{"title":"Organic Synthesis","description":"","products":[{"product_id":"propargyl-peg8-acid","title":"Propargyl-PEG8 Acid","description":"\u003cdiv style=\"max-width: 1400px; margin: 0 auto; padding: 40px 20px; font-family: 'Open Sans', sans-serif; font-weight: 300; background: #fff; color: #333; font-size: 0.95rem; box-sizing: border-box;\"\u003e\n \u003cdiv style=\"display: flex; flex-direction: column; gap: 20px;\"\u003e\n \u003cp\u003e\u003cstrong\u003ePropargyl-PEG8 Acid\u003c\/strong\u003e\u003c\/p\u003e\n \u003cdiv style=\"overflow-x: auto; max-width: 100%; margin-bottom: 20px;\"\u003e\n \u003ctable style=\"width: 500px; border-collapse: collapse;\"\u003e\n \u003ctbody\u003e\n \u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eCatalog number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e B2014795\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eLot number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch Dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eExpiration Date:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eAmount:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 25 mg\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eMolecular Weight or Concentration:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 436.5\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eSupplied as:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Powder\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eApplications:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e molecular tool for various biochemical applications\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eStorage:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e -20 °C\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eKeywords:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Propargyl-PEG8-acid\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eGrade:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity \u0026gt;18 MΩ-cm) and are filtered through 0.22 um.\u003c\/td\u003e\n \u003c\/tr\u003e\n \u003c\/tbody\u003e\n \u003c\/table\u003e\n \u003c\/div\u003e\n\n \u003chr\u003e\n \u003ch4\u003eReferences\u003c\/h4\u003e\n \n \u003cul style=\"padding-left: 20px; margin: 0;\"\u003e\n \u003cli\u003eMero A, Ishino T, Chaiken I, Veronese FM, Pasut G. Multivalent and flexible PEG-nitrilotriacetic acid derivatives for non-covalent protein pegylation Pharm Res. 2011 Oct;28(10):2412-21.\u003c\/li\u003e\n\u003cli\u003eOkutsu T, Kuroiwa Y, Kagitani F, Kai M, Aisaka K, Tsutsumi O, Kaneko Y, Yokomori K, Surani MA, Kohda T, Kaneko-Ishino T, Ishino F. Expression and imprinting status of human PEG8\/IGF2AS, a paternally expressed antisense transcript from the IGF2 locus, in Wilms’ tumors J Biochem. 2000 Mar;127(3):475-83.\u003c\/li\u003e\n\u003cli\u003eDiaferia C, Netti F, Ghosh M, Sibillano T, Giannini C, Morelli G, Adler-Abramovich L, Accardo A. Bi-functional peptide-based 3D hydrogel-scaffolds Soft Matter. 2020 Aug 5;16(30):7006-7017.\u003c\/li\u003e\n\u003cli\u003eShemesh Y, Yavin E. PNA-Rose Bengal Conjugates as Efficient DNA Photomodulators Bioconjug Chem. 2015 Sep 16;26(9):1916-22.\u003c\/li\u003e\n\u003cli\u003eShamsi F. Covalent attachment of three derivatives of pegylated RGD peptides on the NH2-terminated silicon surfaces: Impact on fibroblast cell behavior Biochim Biophys Acta Biomembr. 2021 Dec 1;1863(12):183770.\u003c\/li\u003e\n\u003cli\u003eSamanen J, Narindray D, Adams W Jr, Cash T, Yellin T, Regoli D. Effects of D-amino acid substitution on antagonist activities of angiotensin II analogues J Med Chem. 1988 Mar;31(3):510-6.\u003c\/li\u003e\n\u003cli\u003eBiswas S, Chowdhury PK. Correlated and Anticorrelated Domain Movement of Human Serum Albumin: A Peek into the Complexity of the Crowded Milieu J Phys Chem B. 2016 Jun 9;120(22):4897-911.\u003c\/li\u003e\n\u003cli\u003eChen WH, Lei Q, Luo GF, Jia HZ, Hong S, Liu YX, Cheng YJ, Zhang XZ. Rational Design of Multifunctional Gold Nanoparticles via Host-Guest Interaction for Cancer-Targeted Therapy ACS Appl Mater Interfaces. 2015 Aug 12;7(31):17171-80.\u003c\/li\u003e\n\u003cli\u003eAraújo LM, Thomazine JA, Lopez RF. Development of microemulsions to topically deliver 5-aminolevulinic acid in photodynamic therapy Eur J Pharm Biopharm. 2010 May;75(1):48-55.\u003c\/li\u003e\n \u003c\/ul\u003e\n \u003c\/div\u003e\n \u003c\/div\u003e","brand":"Molecular Depot","offers":[{"title":"Default Title","offer_id":50478263730474,"sku":"BTS-B2014795","price":1167.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0896\/1579\/4474\/files\/B2014795.png?v=1754869397"},{"product_id":"propargyl-peg2-acid","title":"Propargyl-PEG2 Acid","description":"\u003cdiv style=\"max-width: 1400px; margin: 0 auto; padding: 40px 20px; font-family: 'Open Sans', sans-serif; font-weight: 300; background: #fff; color: #333; font-size: 0.95rem; box-sizing: border-box;\"\u003e\n \u003cdiv style=\"display: flex; flex-direction: column; gap: 20px;\"\u003e\n \u003cp\u003e\u003cstrong\u003ePropargyl-PEG2 Acid\u003c\/strong\u003e\u003c\/p\u003e\n \u003cdiv style=\"overflow-x: auto; max-width: 100%; margin-bottom: 20px;\"\u003e\n \u003ctable style=\"width: 500px; border-collapse: collapse;\"\u003e\n \u003ctbody\u003e\n \u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eCatalog number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e B2014798\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eLot number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch Dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eExpiration Date:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eAmount:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 50 mg\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eMolecular Weight or Concentration:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 172.2\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eSupplied as:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Powder\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eApplications:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e molecular tool for various biochemical applications\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eStorage:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e -20 °C\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eKeywords:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Propargyl-PEG2-acid\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eGrade:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity \u0026gt;18 MΩ-cm) and are filtered through 0.22 um.\u003c\/td\u003e\n \u003c\/tr\u003e\n \u003c\/tbody\u003e\n \u003c\/table\u003e\n \u003c\/div\u003e\n\n \u003chr\u003e\n \u003ch4\u003eReferences\u003c\/h4\u003e\n \n \u003cul style=\"padding-left: 20px; margin: 0;\"\u003e\n \u003cli\u003eZhao K, Ke W, Yin W, Li J, Qiang M, Ge Z. Facile Preparation and Radiotherapy Application of an Amphiphilic Block Copolymer Radiosensitizer ACS Macro Lett. 2017 May 16;6(5):556-560.\u003c\/li\u003e\n\u003cli\u003eLiu Y, Wang Y, Zhao J. Design, optimization and in vitro-in vivo evaluation of smart nanocaged carrier delivery of multifunctional PEG-chitosan stabilized silybin nanocrystals Int J Biol Macromol. 2019 Mar 1;124:667-680.\u003c\/li\u003e\n\u003cli\u003eYounis Y, Hunter R, Muhanji CI, Hale I, Singh R, Bailey CM, Sullivan TJ, Anderson KS. [d4U]-spacer-[HI-236] double-drug inhibitors of HIV-1 reverse-transcriptase Bioorg Med Chem. 2010 Jul 1;18(13):4661-73.\u003c\/li\u003e\n\u003cli\u003eLu C, Xing MM, Zhong W. Shell cross-linked and hepatocyte-targeting nanoparticles containing doxorubicin via acid-cleavable linkage Nanomedicine. 2011 Feb;7(1):80-7.\u003c\/li\u003e\n\u003cli\u003eSteinmetz NF, Hong V, Spoerke ED, Lu P, Breitenkamp K, Finn MG, Manchester M. Buckyballs meet viral nanoparticles: candidates for biomedicine J Am Chem Soc. 2009 Dec 2;131(47):17093-5.\u003c\/li\u003e\n\u003cli\u003eDamm D, Kostka K, Weingärtner C, Wagner JT, Rojas-Sánchez L, Gensberger-Reigl S, Sokolova V, Überla K, Epple M, Temchura V. Covalent coupling of HIV-1 glycoprotein trimers to biodegradable calcium phosphate nanoparticles via genetically encoded aldehyde-tags Acta Biomater. 2022 Mar 1;140:586-600.\u003c\/li\u003e\n\u003cli\u003eCheng Y, He C, Xiao C, Ding J, Cui H, Zhuang X, Chen X. Versatile biofunctionalization of polypeptide-based thermosensitive hydrogels via click chemistry Biomacromolecules. 2013 Feb 11;14(2):468-75.\u003c\/li\u003e\n\u003cli\u003eParrish B, Breitenkamp RB, Emrick T. PEG- and peptide-grafted aliphatic polyesters by click chemistry J Am Chem Soc. 2005 May 25;127(20):7404-10.\u003c\/li\u003e\n\u003cli\u003eEgami H, Kamisuki S, Dodo K, Asanuma M, Hamashima Y, Sodeoka M. Catch and release of alkyne-tagged molecules in water by a polymer-supported cobalt complex Org Biomol Chem. 2011 Oct 26;9(22):7667-70.\u003c\/li\u003e\n \u003c\/ul\u003e\n \u003c\/div\u003e\n \u003c\/div\u003e","brand":"Molecular Depot","offers":[{"title":"Default Title","offer_id":50478263763242,"sku":"BTS-B2014798","price":907.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0896\/1579\/4474\/files\/B2014798.png?v=1754869397"},{"product_id":"20-hydroxycholesterol-highly-pure","title":"20-hydroxycholesterol (Highly Pure)","description":"\u003cdiv style=\"max-width: 1400px; margin: 0 auto; padding: 40px 20px; font-family: 'Open Sans', sans-serif; font-weight: 300; background: #fff; color: #333; font-size: 0.95rem; box-sizing: border-box;\"\u003e\n \u003cdiv style=\"display: flex; flex-direction: column; gap: 20px;\"\u003e\n \u003cp\u003e\u003cstrong\u003e20-hydroxycholesterol (Highly Pure)\u003c\/strong\u003e\u003c\/p\u003e\n \u003cdiv style=\"overflow-x: auto; max-width: 100%; margin-bottom: 20px;\"\u003e\n \u003ctable style=\"width: 500px; border-collapse: collapse;\"\u003e\n \u003ctbody\u003e\n \u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eCatalog number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e B2014819\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eLot number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch Dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eExpiration Date:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eAmount:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 1 mg\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eMolecular Weight or Concentration:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e N\/A\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eSupplied as:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e N\/A\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eApplications:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e molecular tool for various biochemical applications\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eStorage:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e RT\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eKeywords:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 20-hydroxycholesterol\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eGrade:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity \u0026gt;18 MΩ-cm) and are filtered through 0.22 um.\u003c\/td\u003e\n \u003c\/tr\u003e\n \u003c\/tbody\u003e\n \u003c\/table\u003e\n \u003c\/div\u003e\n\n \u003chr\u003e\n \u003ch4\u003eReferences\u003c\/h4\u003e\n \n \u003cul style=\"padding-left: 20px; margin: 0;\"\u003e\n \u003cli\u003eHuang Y, Lin Y, Rong M, Liu W, He J, Zhou L. 20(S)-hydroxycholesterol and simvastatin synergistically enhance osteogenic differentiation of marrow stromal cells and bone regeneration by initiation of Raf\/MEK\/ERK signaling J Mater Sci Mater Med. 2019 Jul 19;30(8):87.\u003c\/li\u003e\n\u003cli\u003eFaletrov YV, Efimova VS, Horetski MS, Tugaeva KV, Frolova NS, Lin Q, Isaeva LV, Rubtsov MA, Sluchanko NN, Novikova LA, Shkumatov VM. New 20-hydroxycholesterol-like compounds with fluorescent NBD or alkyne labels: Synthesis, in silico interactions with proteins and uptake by yeast cells Chem Phys Lipids. 2020 Mar;227:104850.\u003c\/li\u003e\n\u003cli\u003eAdhikari R, Chen C, Kim WK. Effect of 20(S)-Hydroxycholesterol on Multilineage Differentiation of Mesenchymal Stem Cells Isolated from Compact Bones in Chicken Genes (Basel). 2020 Nov 17;11(11):1360.\u003c\/li\u003e\n\u003cli\u003eCONSTANTOPOULOS G, TCHEN TT. Conversion of 20-alpha-hydroxycholesterol to pregnenolone Biochem Biophys Res Commun. 1961 Apr 28;4:460-3.\u003c\/li\u003e\n\u003cli\u003eMijares A, Cargill DI, Glasel JA, Lieberman S. Studies on the C-20 epimers of 20-hydroxycholesterol J Org Chem. 1967 Mar;32(3):810-2.\u003c\/li\u003e\n\u003cli\u003eKim WK, Meliton V, Amantea CM, Hahn TJ, Parhami F. 20(S)-hydroxycholesterol inhibits PPARgamma expression and adipogenic differentiation of bone marrow stromal cells through a hedgehog-dependent mechanism J Bone Miner Res. 2007 Nov;22(11):1711-9.\u003c\/li\u003e\n\u003cli\u003eBurstein S, Middleditch BS, Gut M. Mass spectrometric study of the enzymatic conversion of cholesterol to (22R)-22-hydroxycholesterol, (20R,22R)-20,22-dihydroxycholesterol, and pregnenolone, and of (22R)-22-hydroxycholesterol to the lgycol and pregnenolone in bovine adrenocortical preparations. Mode of oxygen incorporation J Biol Chem. 1975 Dec 10;250(23):9028-37.\u003c\/li\u003e\n\u003cli\u003eHALL PF, KORITZ SB. INHIBITION OF THE BIOSYNTHESIS OF PREGNENOLONE BY 20-ALPHA-HYDROXYCHOLESTEROL Biochim Biophys Acta. 1964 Nov 8;93:441-4.\u003c\/li\u003e\n\u003cli\u003eSHIMIZU K, DORFMAN RI, GUT M. Isocaproic acid, a metabolite of 20 alpha-hydroxycholesterol J Biol Chem. 1960 Jun;235:PC25.\u003c\/li\u003e\n \u003c\/ul\u003e\n \u003c\/div\u003e\n \u003c\/div\u003e","brand":"Molecular Depot","offers":[{"title":"Default Title","offer_id":50478263861546,"sku":"BTS-B2014819","price":1167.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0896\/1579\/4474\/files\/B2014819.png?v=1754869403"},{"product_id":"5-hydroxyindole-2-carboxylic-acid-highly-pure","title":"5-Hydroxyindole-2-carboxylic Acid (Highly Pure)","description":"\u003cdiv style=\"max-width: 1400px; margin: 0 auto; padding: 40px 20px; font-family: 'Open Sans', sans-serif; font-weight: 300; background: #fff; color: #333; font-size: 0.95rem; box-sizing: border-box;\"\u003e\n \u003cdiv style=\"display: flex; flex-direction: column; gap: 20px;\"\u003e\n \u003cp\u003e\u003cstrong\u003e5-Hydroxyindole-2-carboxylic Acid (Highly Pure)\u003c\/strong\u003e\u003c\/p\u003e\n \u003cdiv style=\"overflow-x: auto; max-width: 100%; margin-bottom: 20px;\"\u003e\n \u003ctable style=\"width: 500px; border-collapse: collapse;\"\u003e\n \u003ctbody\u003e\n \u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eCatalog number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e B2016293\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eLot number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch Dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eExpiration Date:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eAmount:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 5 g\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eMolecular Weight or Concentration:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 177.16 g\/mol\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eSupplied as:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Powder\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eApplications:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e a molecular tool for various biochemical applications\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eStorage:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e -20°C\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eKeywords:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 5-Hydroxyindole-2-carboxylic acid\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eGrade:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity \u0026gt;18 MΩ-cm) and are filtered through 0.22 um.\u003c\/td\u003e\n \u003c\/tr\u003e\n \u003c\/tbody\u003e\n \u003c\/table\u003e\n \u003c\/div\u003e\n\n \u003chr\u003e\n \u003ch4\u003eReferences\u003c\/h4\u003e\n \n \u003cul style=\"padding-left: 20px; margin: 0;\"\u003e\n \u003cli\u003ePierson PD, Fettes A, Freichel C, Gatti-McArthur S, Hertel C, Huwyler J, Mohr P, Nakagawa T, Nettekoven M, Plancher JM, Raab S, Richter H, Roche O, Rodríguez Sarmiento RM, Schmitt M, Schuler F, Takahashi T, Taylor S, Ullmer C, Wiegand R. 5-hydroxyindole-2-carboxylic acid amides: novel histamine-3 receptor inverse agonists for the treatment of obesity J Med Chem. 2009 Jul 9;52(13):3855-68.\u003c\/li\u003e\n\u003cli\u003eAroca P, Solano F, Garcia-Borrón JC, Lozano JA. Specificity of dopachrome tautomerase and inhibition by carboxylated indoles. Considerations on the enzyme active site Biochem J. 1991 Jul 15;277 ( Pt 2)(Pt 2):393-7.\u003c\/li\u003e\n\u003cli\u003eCuevas AA, García-Castiñeiras S. Melanins and lens pigments: a comparative study P R Health Sci J. 1993 Jun;12(2):129-35.\u003c\/li\u003e\n\u003cli\u003eRitschdorff ET, Plenert ML, Shear JB. Microsecond analysis of transient molecules using bi-directional capillary electrophoresis Anal Chem. 2009 Nov 1;81(21):8790-6.\u003c\/li\u003e\n\u003cli\u003eDu F, Zhou Q, Sun W, Yang C, Wu C, Wang L, Chen G. 5-Hydroxyindole-Based EZH2 Inhibitors Assembled via TCCA-Catalyzed Condensation and Nenitzescu Reactions Molecules. 2020 Apr 28;25(9):2059.\u003c\/li\u003e\n\u003cli\u003eWaclawiková B, Bullock A, Schwalbe M, Aranzamendi C, Nelemans SA, van Dijk G, El Aidy S. Gut bacteria-derived 5-hydroxyindole is a potent stimulant of intestinal motility via its action on L-type calcium channels PLoS Biol. 2021 Jan 22;19(1):e3001070.\u003c\/li\u003e\n\u003cli\u003eSouthgate J, Sandler M. 5-hydroxyindole metabolism in pregnancy Adv Pharmacol (1962). 1968;6(Pt B):179-86.\u003c\/li\u003e\n\u003cli\u003eMoroni F, Carpenedo R, Mannaioni G, Galli A, Chiarugi A, Carlà V, Moneti G. Studies on the pharmacological properties of oxindole (2-hydroxyindole) and 5-hydroxyindole: are they involved in hepatic encephalopathy? Adv Exp Med Biol. 1997;420:57-73.\u003c\/li\u003e\n\u003cli\u003eFredj Z, Ali M, Singh B, Dempsey E. Simultaneous voltammetric detection of 5-hydroxyindole-3-acetic acid and 5-hydroxytryptamine using a glassy carbon electrode modified with conducting polymer and platinised carbon nanofibers Mikrochim Acta. 2018 Aug 13;185(9):412.\u003c\/li\u003e\n \u003c\/ul\u003e\n \u003c\/div\u003e\n \u003c\/div\u003e","brand":"Molecular Depot","offers":[{"title":"Default Title","offer_id":50482767528234,"sku":"BTS-B2016293","price":1595.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0896\/1579\/4474\/files\/B2016293.png?v=1754943013"},{"product_id":"calcium-acetate-hydrate","title":"Calcium Acetate Hydrate","description":"\u003cdiv style=\"max-width: 1400px; margin: 0 auto; padding: 40px 20px; font-family: 'Open Sans', sans-serif; font-weight: 300; background: #fff; color: #333; font-size: 0.95rem; box-sizing: border-box;\"\u003e\n \u003cdiv style=\"display: flex; flex-direction: column; gap: 20px;\"\u003e\n \u003cp\u003e\u003cstrong\u003eCalcium Acetate Hydrate\u003c\/strong\u003e\u003c\/p\u003e\n \u003cdiv style=\"overflow-x: auto; max-width: 100%; margin-bottom: 20px;\"\u003e\n \u003ctable style=\"width: 500px; border-collapse: collapse;\"\u003e\n \u003ctbody\u003e\n \u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eCatalog number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e B2016288\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eLot number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch Dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eExpiration Date:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eAmount:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 50 g\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eMolecular Weight or Concentration:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 158.17 (anhydrous basis)\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eSupplied as:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Powder\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eApplications:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e a molecular tool for various biochemical applications\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eStorage:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Dry, RT\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eKeywords:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Calcium acetate hydrate\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eGrade:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity \u0026gt;18 MΩ-cm) and are filtered through 0.22 um.\u003c\/td\u003e\n \u003c\/tr\u003e\n \u003c\/tbody\u003e\n \u003c\/table\u003e\n \u003c\/div\u003e\n\n \u003chr\u003e\n \u003ch4\u003eReferences\u003c\/h4\u003e\n \n \u003cul style=\"padding-left: 20px; margin: 0;\"\u003e\n \u003cli\u003eClark B, Baqdunes MW, Kunkel GM. Diet-induced oxalate nephropathy BMJ Case Rep. 2019 Sep 16;12(9):e231284.\u003c\/li\u003e\n\u003cli\u003eDaugirdas JT, Finn WF, Emmett M, Chertow GM; Frequent Hemodialysis Network Trial Group. The phosphate binder equivalent dose Semin Dial. 2011 Jan-Feb;24(1):41-9.\u003c\/li\u003e\n\u003cli\u003eLiu S, Cui S, Guo H, Wang Y, Zheng Y. Adsorption of Lead Ion from Wastewater Using Non-Crystal Hydrated Calcium Silicate Gel Materials (Basel). 2021 Feb 10;14(4):842.\u003c\/li\u003e\n\u003cli\u003eMusumeci AW, Frost RL, Waclawik ER. A spectroscopic study of the mineral paceite (calcium acetate) Spectrochim Acta A Mol Biomol Spectrosc. 2007 Jul;67(3-4):649-61.\u003c\/li\u003e\n\u003cli\u003eLiu W, Low NW, Feng B, Wang G, Diniz da Costa JC. Calcium precursors for the production of CaO sorbents for multicycle CO2 capture Environ Sci Technol. 2010 Jan 15;44(2):841-7.\u003c\/li\u003e\n\u003cli\u003eAl-Amin MD, Bellato F, Mastrotto F, Garofalo M, Malfanti A, Salmaso S, Caliceti P. Dexamethasone Loaded Liposomes by Thin-Film Hydration and Microfluidic Procedures: Formulation Challenges Int J Mol Sci. 2020 Feb 26;21(5):1611.\u003c\/li\u003e\n\u003cli\u003eNik ME, Malaekeh-Nikouei B, Amin M, Hatamipour M, Teymouri M, Sadeghnia HR, Iranshahi M, Jaafari MR. Liposomal formulation of Galbanic acid improved therapeutic efficacy of pegylated liposomal Doxorubicin in mouse colon carcinoma Sci Rep. 2019 Jul 2;9(1):9527.\u003c\/li\u003e\n\u003cli\u003eZhang A, Liu J, Yang Y, Li Y. Insights into chromium removal mechanism by Ca-based sorbents from flue gas Sci Total Environ. 2024 Feb 20;912:168928.\u003c\/li\u003e\n\u003cli\u003eTang H, Li C, Duan Y, Zhu C, Cai L. Combined experimental and theoretical studies on adsorption mechanisms of gaseous mercury(II) by calcium-based sorbents: The effect of unsaturated oxygen sites Sci Total Environ. 2019 Mar 15;656:937-945.\u003c\/li\u003e\n \u003c\/ul\u003e\n \u003c\/div\u003e\n \u003c\/div\u003e","brand":"Molecular Depot","offers":[{"title":"Default Title","offer_id":50482767823146,"sku":"BTS-B2016288","price":595.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0896\/1579\/4474\/files\/B2016288.png?v=1754943014"},{"product_id":"5-methoxyindole-highly-pure","title":"5-Methoxyindole (Highly Pure)","description":"\u003cdiv style=\"max-width: 1400px; margin: 0 auto; padding: 40px 20px; font-family: 'Open Sans', sans-serif; font-weight: 300; background: #fff; color: #333; font-size: 0.95rem; box-sizing: border-box;\"\u003e\n \u003cdiv style=\"display: flex; flex-direction: column; gap: 20px;\"\u003e\n \u003cp\u003e\u003cstrong\u003e5-Methoxyindole (Highly Pure)\u003c\/strong\u003e\u003c\/p\u003e\n \u003cdiv style=\"overflow-x: auto; max-width: 100%; margin-bottom: 20px;\"\u003e\n \u003ctable style=\"width: 500px; border-collapse: collapse;\"\u003e\n \u003ctbody\u003e\n \u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eCatalog number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e B2016301\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eLot number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch Dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eExpiration Date:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eAmount:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 25 g\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eMolecular Weight or Concentration:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 147.18 g\/mol\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eSupplied as:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Powder\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eApplications:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e a molecular tool for various biochemical applications\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eStorage:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e -20°C\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eKeywords:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Indol-5-yl methyl ether\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eGrade:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity \u0026gt;18 MΩ-cm) and are filtered through 0.22 um.\u003c\/td\u003e\n \u003c\/tr\u003e\n \u003c\/tbody\u003e\n \u003c\/table\u003e\n \u003c\/div\u003e\n\n \u003chr\u003e\n \u003ch4\u003eReferences\u003c\/h4\u003e\n \n \u003cul style=\"padding-left: 20px; margin: 0;\"\u003e\n \u003cli\u003eIndomethacin 2021 Jan 18. Drugs and Lactation Database (LactMed®) [Internet]. Bethesda (MD): National Institute of Child Health and Human Development; 2006–.\u003c\/li\u003e\n\u003cli\u003eHo S, Pang SF, Tsang CW, Tang PL. Effect of light on 5-methoxyindole-3-acetic acid in the rat J Neural Transm (Vienna). 2001;108(5):503-11.\u003c\/li\u003e\n\u003cli\u003eHiga S, Markey SP. Identification and quantification of 5-methoxyindole-3-acetic acid in human urine Anal Biochem. 1985 Jan;144(1):86-93.\u003c\/li\u003e\n\u003cli\u003eWang HX, Ng TB. Demonstration of antifungal and anti-human immunodeficiency virus reverse transcriptase activities of 6-methoxy-2-benzoxazolinone and antibacterial activity of the pineal indole 5-methoxyindole-3-acetic acid Comp Biochem Physiol C Toxicol Pharmacol. 2002 Jun;132(2):261-8.\u003c\/li\u003e\n\u003cli\u003eHardeland R. Taxon- and Site-Specific Melatonin Catabolism Molecules. 2017 Nov 21;22(11):2015.\u003c\/li\u003e\n\u003cli\u003ePévet P, Balemans MG, de Reuver GF. The pineal gland of the mole (Talpa europaea L.). VII. Activity of hydroxyindole-O-methyltransferase (HIOMT) in the formation of 5-methoxytryptophan, 5-methoxytryptamine, 5-methoxyindole-3-acetic acid, 5-methoxytryptophol and melantonin in the eyes and the pineal gland J Neural Transm. 1981;51(3-4):271-82.\u003c\/li\u003e\n\u003cli\u003eLi P, Pang SF, Tsang CW. Retinal 5-methoxytryptamine and 5-methoxyindole-3-acetic acid in the rat and quail: diurnal rhythms and interspecies differences Biochem Biophys Res Commun. 1997 Oct 9;239(1):353-6.\u003c\/li\u003e\n\u003cli\u003eLERNER AB, CASE JD, TAKAHASHI Y. Isolation of melatonin and 5-methoxyindole-3-acetic acid from bovine pineal glands J Biol Chem. 1960 Jul;235:1992-7.\u003c\/li\u003e\n\u003cli\u003eOcal-Irez T, Durmus G, Sekerkiran Y, Peker C, Uygur G. Effect of a pineal indolamine, 5-methoxyindole-3-acetic acid, on the estrous cycle and reproductive organs of female Wistar albino rats Brain Res. 1989 Jul 24;493(1):1-7.\u003c\/li\u003e\n \u003c\/ul\u003e\n \u003c\/div\u003e\n \u003c\/div\u003e","brand":"Molecular Depot","offers":[{"title":"Default Title","offer_id":50482767921450,"sku":"BTS-B2016301","price":907.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0896\/1579\/4474\/files\/B2016301.png?v=1754943020"},{"product_id":"5-methoxy-2-methylindole-highly-pure","title":"5-Methoxy-2-methylindole (Highly Pure)","description":"\u003cdiv style=\"max-width: 1400px; margin: 0 auto; padding: 40px 20px; font-family: 'Open Sans', sans-serif; font-weight: 300; background: #fff; color: #333; font-size: 0.95rem; box-sizing: border-box;\"\u003e\n \u003cdiv style=\"display: flex; flex-direction: column; gap: 20px;\"\u003e\n \u003cp\u003e\u003cstrong\u003e5-Methoxy-2-methylindole (Highly Pure)\u003c\/strong\u003e\u003c\/p\u003e\n \u003cdiv style=\"overflow-x: auto; max-width: 100%; margin-bottom: 20px;\"\u003e\n \u003ctable style=\"width: 500px; border-collapse: collapse;\"\u003e\n \u003ctbody\u003e\n \u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eCatalog number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e B2016304\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eLot number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch Dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eExpiration Date:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eAmount:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 250 mg\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eMolecular Weight or Concentration:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 161.21 g\/mol\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eSupplied as:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Powder\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eApplications:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e a molecular tool for various biochemical applications\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eStorage:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 2-8°C\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eKeywords:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 5-Methoxy-2-methylindole\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eGrade:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity \u0026gt;18 MΩ-cm) and are filtered through 0.22 um.\u003c\/td\u003e\n \u003c\/tr\u003e\n \u003c\/tbody\u003e\n \u003c\/table\u003e\n \u003c\/div\u003e\n\n \u003chr\u003e\n \u003ch4\u003eReferences\u003c\/h4\u003e\n \n \u003cul style=\"padding-left: 20px; margin: 0;\"\u003e\n \u003cli\u003eIndomethacin 2021 Jan 18. Drugs and Lactation Database (LactMed®) [Internet]. Bethesda (MD): National Institute of Child Health and Human Development; 2006–.\u003c\/li\u003e\n\u003cli\u003eTanaka I, Yoshizumi H, Tanaka Y, Takeda S, Kamei C, Nakaya N, Kitazumi K, Tagami H, Tasaka K. Pharmacological profiles of 2-carboxyphenyl-1-(4-chlorobenzoyl)-5-methoxy-2-methylindole-3-acetate and 2-[(2-carboxyphenoxy)-carbonyl]phenyl-1-(4-chlorobenzoyl)-5-meth oxy-2- methylindole-3-acetate, new antiinflammatory agents Arzneimittelforschung. 1986 Apr;36(4):703-9.\u003c\/li\u003e\n\u003cli\u003eWINTER CA, RISLEY EA, NUSS GW. ANTI-INFLAMMATORY AND ANTIPYRETIC ACTIVITIES OF INDOMETHACIN, 1-(P-CHLOROBENZOYL)-5-METHOXY-2-METHYLINDOLE-3-ACETIC ACID J Pharmacol Exp Ther. 1963 Sep;141:369-76.\u003c\/li\u003e\n\u003cli\u003eParis GY, Garmaise DL, Cimon DG, Swett L, Carter GW, Young P. Glycerides as prodrugs. 3. Synthesis and antiinflammatory activity of [1-(p-chlorobenzoyl)-5-methoxy-2-methylindole-3-acetyl]glycerides (indomethacin glycerides) J Med Chem. 1980 Jan;23(1):9-13.\u003c\/li\u003e\n\u003cli\u003eO’Hara E, Seymour J. Inducing metamorphosis in the irukandji jellyfish Carukia barnesi Sci Rep. 2022 May 31;12(1):9052.\u003c\/li\u003e\n\u003cli\u003eGiordano M, Capelli L, Chianese U. The therapeutic activity of 1-(p-chlorobenzoyl)-5-methoxy-2-methylindole-3-acetic acid monohydrate glucosamide in rheumatoid arthritis (double blind trial) Arzneimittelforschung. 1975 Mar;25(3):435-7.\u003c\/li\u003e\n\u003cli\u003eUeda I, Ishii K, Arai H, Ikeda S, Hitomi Y, Hatanaka M. Design, synthesis and antiinflammatory activity of a new indomethacin ester. 2-[N-[3-(3-(piperidinomethyl)phenoxy)propyl]carbamoylmethylthio]ethyl 1-(p-chlorobenzoyl)-5-methoxy-2-methyl-indole-3-acetate Chem Pharm Bull (Tokyo). 1991 Mar;39(3):679-84.\u003c\/li\u003e\n\u003cli\u003eHelleberg L. Clinical Pharmacokinetics of indomethacin Clin Pharmacokinet. 1981 Jul-Aug;6(4):245-58.\u003c\/li\u003e\n\u003cli\u003eKistenmacher TJ, Marsh RE. Crystal and molecular structure of an antiinflammatory agent, indomethacin, 1-(p-chlorobenzoyl)-5-methoxy-2-methylindole-3-acetic acid J Am Chem Soc. 1972 Feb 23;94(4):1340-5.\u003c\/li\u003e\n \u003c\/ul\u003e\n \u003c\/div\u003e\n \u003c\/div\u003e","brand":"Molecular Depot","offers":[{"title":"Default Title","offer_id":50482767954218,"sku":"BTS-B2016304","price":907.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0896\/1579\/4474\/files\/B2016304.png?v=1754943020"},{"product_id":"5-chloroindole-highly-pure","title":"5-Chloroindole (Highly Pure)","description":"\u003cdiv style=\"max-width: 1400px; margin: 0 auto; padding: 40px 20px; font-family: 'Open Sans', sans-serif; font-weight: 300; background: #fff; color: #333; font-size: 0.95rem; box-sizing: border-box;\"\u003e\n \u003cdiv style=\"display: flex; flex-direction: column; gap: 20px;\"\u003e\n \u003cp\u003e\u003cstrong\u003e5-Chloroindole (Highly Pure)\u003c\/strong\u003e\u003c\/p\u003e\n \u003cdiv style=\"overflow-x: auto; max-width: 100%; margin-bottom: 20px;\"\u003e\n \u003ctable style=\"width: 500px; border-collapse: collapse;\"\u003e\n \u003ctbody\u003e\n \u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eCatalog number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e B2016295\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eLot number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch Dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eExpiration Date:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eAmount:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 10 g\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eMolecular Weight or Concentration:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 151.60 g\/mol\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eSupplied as:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Powder\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eApplications:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e a molecular tool for various biochemical applications\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eStorage:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 2-8°C\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eKeywords:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 5-Chloroindole\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eGrade:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity \u0026gt;18 MΩ-cm) and are filtered through 0.22 um.\u003c\/td\u003e\n \u003c\/tr\u003e\n \u003c\/tbody\u003e\n \u003c\/table\u003e\n \u003c\/div\u003e\n\n \u003chr\u003e\n \u003ch4\u003eReferences\u003c\/h4\u003e\n \n \u003cul style=\"padding-left: 20px; margin: 0;\"\u003e\n \u003cli\u003eNewman AS, Batis N, Grafton G, Caputo F, Brady CA, Lambert JJ, Peters JA, Gordon J, Brain KL, Powell AD, Barnes NM. 5-Chloroindole: a potent allosteric modulator of the 5-HT₃ receptor Br J Pharmacol. 2013 Jul;169(6):1228-38.\u003c\/li\u003e\n\u003cli\u003eJensen JB, Egsgaard H, Van Onckelen H, Jochimsen BU. Catabolism of indole-3-acetic acid and 4- and 5-chloroindole-3-acetic acid in Bradyrhizobium japonicum J Bacteriol. 1995 Oct;177(20):5762-6.\u003c\/li\u003e\n\u003cli\u003ePrice KL, Lummis SCR. Characterization of a 5-HT(3)-ELIC Chimera Revealing the Sites of Action of Modulators ACS Chem Neurosci. 2018 Jun 20;9(6):1409-1415.\u003c\/li\u003e\n\u003cli\u003eYoussif BGM, Mohamed AM, Osman EEA, Abou-Ghadir OF, Elnaggar DH, Abdelrahman MH, Treamblu L, Gomaa HAM. 5-Chlorobenzofuran-2-carboxamides: From allosteric CB1 modulators to potential apoptotic antitumor agents Eur J Med Chem. 2019 Sep 1;177:1-11.\u003c\/li\u003e\n\u003cli\u003eKholodar SA, Lang G, Cortopassi WA, Iizuka Y, Brah HS, Jacobson MP, England PM. Analogs of the Dopamine Metabolite 5,6-Dihydroxyindole Bind Directly to and Activate the Nuclear Receptor Nurr1 ACS Chem Biol. 2021 Jul 16;16(7):1159-1163.\u003c\/li\u003e\n\u003cli\u003eSural S, Botero JQ, Hobert O, Tekle-Smith M. Protocol to synthesize the auxin analog 5-Ph-IAA for conditional protein depletion in C. elegans using the AID2 system STAR Protoc. 2024 Mar 15;5(1):102901.\u003c\/li\u003e\n\u003cli\u003eBoya BR, Lee JH, Lee J. Antibiofilm and Antimicrobial Activities of Chloroindoles Against Uropathogenic Escherichia coli Front Microbiol. 2022 Jun 16;13:872943.\u003c\/li\u003e\n\u003cli\u003eYan Z, Li S, Wang Y, Li J, Ma C, Guo Y, Zhang L. Discovery of novel heterocyclic derivatives as potential glycogen phosphorylase inhibitors with a cardioprotective effect Bioorg Chem. 2022 Dec;129:106120.\u003c\/li\u003e\n\u003cli\u003eXu L, Sun H. Pharmacological manipulation of brain glycogenolysis as a therapeutic approach to cerebral ischemia Mini Rev Med Chem. 2010 Oct;10(12):1188-93.\u003c\/li\u003e\n \u003c\/ul\u003e\n \u003c\/div\u003e\n \u003c\/div\u003e","brand":"Molecular Depot","offers":[{"title":"Default Title","offer_id":50482768216362,"sku":"BTS-B2016295","price":907.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0896\/1579\/4474\/files\/B2016295.png?v=1754943021"},{"product_id":"5-bromoindole-2-carboxylic-acid-highly-pure","title":"5-Bromoindole-2-carboxylic Acid (Highly Pure)","description":"\u003cdiv style=\"max-width: 1400px; margin: 0 auto; padding: 40px 20px; font-family: 'Open Sans', sans-serif; font-weight: 300; background: #fff; color: #333; font-size: 0.95rem; box-sizing: border-box;\"\u003e\n \u003cdiv style=\"display: flex; flex-direction: column; gap: 20px;\"\u003e\n \u003cp\u003e\u003cstrong\u003e5-Bromoindole-2-carboxylic Acid (Highly Pure)\u003c\/strong\u003e\u003c\/p\u003e\n \u003cdiv style=\"overflow-x: auto; max-width: 100%; margin-bottom: 20px;\"\u003e\n \u003ctable style=\"width: 500px; border-collapse: collapse;\"\u003e\n \u003ctbody\u003e\n \u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eCatalog number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e B2016305\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eLot number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch Dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eExpiration Date:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eAmount:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 5 g\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eMolecular Weight or Concentration:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 240.06 g\/mol\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eSupplied as:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Powder\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eApplications:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e a molecular tool for various biochemical applications\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eStorage:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e -20°C\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eKeywords:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 5-Bromoindole-2-carboxylic acid\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eGrade:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity \u0026gt;18 MΩ-cm) and are filtered through 0.22 um.\u003c\/td\u003e\n \u003c\/tr\u003e\n \u003c\/tbody\u003e\n \u003c\/table\u003e\n \u003c\/div\u003e\n\n \u003chr\u003e\n \u003ch4\u003eReferences\u003c\/h4\u003e\n \n \u003cul style=\"padding-left: 20px; margin: 0;\"\u003e\n \u003cli\u003eHassan OM, Kubba A, Tahtamouni LH. Novel 5-bromoindole-2-carboxylic Acid Derivatives as EGFR Inhibitors: Synthesis, Docking Study, and Structure Activity Relationship Anticancer Agents Med Chem. 2023;23(11):1336-1348.\u003c\/li\u003e\n\u003cli\u003eJahangir S, Eglin D, Pötter N, Khozaei Ravari M, Stoddart MJ, Samadikuchaksaraei A, Alini M, Baghaban Eslaminejad M, Safa M. Inhibition of hypertrophy and improving chondrocyte differentiation by MMP-13 inhibitor small molecule encapsulated in alginate-chondroitin sulfate-platelet lysate hydrogel Stem Cell Res Ther. 2020 Oct 9;11(1):436.\u003c\/li\u003e\n\u003cli\u003eHassan OM, Kubba A, Tahtamouni LH. Novel 5-bromoindole-2-carboxylic Acid Derivatives as EGFR Inhibitors: Synthesis, Docking Study, and Structure Activity Relationship Anticancer Agents Med Chem. 2023;23(11):1336-1348.\u003c\/li\u003e\n\u003cli\u003eJahangir S, Eglin D, Pötter N, Khozaei Ravari M, Stoddart MJ, Samadikuchaksaraei A, Alini M, Baghaban Eslaminejad M, Safa M. Inhibition of hypertrophy and improving chondrocyte differentiation by MMP-13 inhibitor small molecule encapsulated in alginate-chondroitin sulfate-platelet lysate hydrogel Stem Cell Res Ther. 2020 Oct 9;11(1):436.\u003c\/li\u003e\n\u003cli\u003eKhan M. The antischistosomal activity of substituted indoles J Environ Sci Health B. 1983 Dec;18(6):781-93.\u003c\/li\u003e\n\u003cli\u003eManoso AS, Ahn C, Soheili A, Handy CJ, Correia R, Seganish WM, Deshong P. Improved synthesis of aryltrialkoxysilanes via treatment of aryl Grignard or lithium reagents with tetraalkyl orthosilicates J Org Chem. 2004 Nov 26;69(24):8305-14.\u003c\/li\u003e\n\u003cli\u003eMeyer A, Würsten M, Schmid A, Kohler HP, Witholt B. Hydroxylation of indole by laboratory-evolved 2-hydroxybiphenyl 3-monooxygenase J Biol Chem. 2002 Sep 13;277(37):34161-7.\u003c\/li\u003e\n\u003cli\u003eYan X, Tang XX, Qin D, Yi ZW, Fang MJ, Wu Z, Qiu YK. Biosynthetic Functional Gene Analysis of Bis-Indole Metabolites from 25D7, a Clone Derived from a Deep-Sea Sediment Metagenomic Library Mar Drugs. 2016 Jun 1;14(6):107.\u003c\/li\u003e\n\u003cli\u003eMunir IZ, Dordick JS. Soybean peroxidase as an effective bromination catalyst* Enzyme Microb Technol. 2000 Mar 1;26(5-6):337-341.\u003c\/li\u003e\n \u003c\/ul\u003e\n \u003c\/div\u003e\n \u003c\/div\u003e","brand":"Molecular Depot","offers":[{"title":"Default Title","offer_id":50482768249130,"sku":"BTS-B2016305","price":907.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0896\/1579\/4474\/files\/B2016305.png?v=1754943022"},{"product_id":"tyramine-free-base","title":"Tyramine Free Base","description":"\u003cdiv style=\"max-width: 1400px; margin: 0 auto; padding: 40px 20px; font-family: 'Open Sans', sans-serif; font-weight: 300; background: #fff; color: #333; font-size: 0.95rem; box-sizing: border-box;\"\u003e\n \u003cdiv style=\"display: flex; flex-direction: column; gap: 20px;\"\u003e\n \u003cp\u003e\u003cstrong\u003eTyramine Free Base\u003c\/strong\u003e\u003c\/p\u003e\n \u003cdiv style=\"overflow-x: auto; max-width: 100%; margin-bottom: 20px;\"\u003e\n \u003ctable style=\"width: 500px; border-collapse: collapse;\"\u003e\n \u003ctbody\u003e\n \u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eCatalog number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e B2016296\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eLot number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch Dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eExpiration Date:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eAmount:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 100 g\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eMolecular Weight or Concentration:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 137.18 g\/mol\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eSupplied as:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Powder\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eApplications:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e a molecular tool for various biochemical applications\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eStorage:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 2-8°C\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eKeywords:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Tyramine, free base\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eGrade:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity \u0026gt;18 MΩ-cm) and are filtered through 0.22 um.\u003c\/td\u003e\n \u003c\/tr\u003e\n \u003c\/tbody\u003e\n \u003c\/table\u003e\n \u003c\/div\u003e\n\n \u003chr\u003e\n \u003ch4\u003eReferences\u003c\/h4\u003e\n \n \u003cul style=\"padding-left: 20px; margin: 0;\"\u003e\n \u003cli\u003eFan D, Zhu X, Dong S, Wang E. Tyramine Hydrochloride Based Label-Free System for Operating Various DNA Logic Gates and a DNA Caliper for Base Number Measurements Chemphyschem. 2017 Jul 5;18(13):1767-1772.\u003c\/li\u003e\n\u003cli\u003eRaman N, Sobha S, Thamaraichelvan A. A novel bioactive tyramine derived Schiff base and its transition metal complexes as selective DNA binding agents Spectrochim Acta A Mol Biomol Spectrosc. 2011 Feb;78(2):888-98.\u003c\/li\u003e\n\u003cli\u003eMitsuda H, Kawai F, Yamamoto A, Nakajima K. Carbon dioxide-protein interaction in a gas-solid phase J Nutr Sci Vitaminol (Tokyo). 1975;21(3):151-62.\u003c\/li\u003e\n\u003cli\u003eChotimarkorn C, Silalai N, Chaitanawisuit N. Post-mortem changes in farmed spotted Babylon snail (Babylonia areolata) during iced storage Food Sci Technol Int. 2010 Jun;16(3):277-84.\u003c\/li\u003e\n\u003cli\u003eCueva C, García-Ruiz A, González-Rompinelli E, Bartolome B, Martín-Álvarez PJ, Salazar O, Vicente MF, Bills GF, Moreno-Arribas MV. Degradation of biogenic amines by vineyard ecosystem fungi. Potential use in winemaking J Appl Microbiol. 2012 Apr;112(4):672-82.\u003c\/li\u003e\n\u003cli\u003eGuo X, Zang X, Dou SJ, Wang DY, Wang XL. Fermentation of soymilk by Lactobacillus acidipiscis isolated from Chinese stinky tofu capable of efficiently biotransforming isoflavone glucosides to dihydrodaidzein and dihydrogenistein J Sci Food Agric. 2022 Dec;102(15):7221-7230.\u003c\/li\u003e\n\u003cli\u003eDong J, Cui X, Deng Y, Tang Z. Amplified detection of nucleic acid by G-quadruplex based hybridization chain reaction Biosens Bioelectron. 2012 Oct-Dec;38(1):258-63.\u003c\/li\u003e\n\u003cli\u003eMundorf ML, Hochstetler SE, Wightman RM. Amine weak bases disrupt vesicular storage and promote exocytosis in chromaffin cells J Neurochem. 1999 Dec;73(6):2397-405.\u003c\/li\u003e\n\u003cli\u003eByrne-Quinn E, Grover RF. Aminorex (Menocil) and amphetamine: acute and chronic effects on pulmonary and systemic haemodynamics in the calf Thorax. 1972 Jan;27(1):127-31.\u003c\/li\u003e\n \u003c\/ul\u003e\n \u003c\/div\u003e\n \u003c\/div\u003e","brand":"Molecular Depot","offers":[{"title":"Default Title","offer_id":50482768314666,"sku":"BTS-B2016296","price":795.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0896\/1579\/4474\/files\/B2016296.png?v=1754943027"},{"product_id":"triton-x-114-10","title":"Triton X-114 10%","description":"\u003cdiv style=\"max-width: 1400px; margin: 0 auto; padding: 40px 20px; font-family: 'Open Sans', sans-serif; font-weight: 300; background: #fff; color: #333; font-size: 0.95rem; box-sizing: border-box;\"\u003e\n \u003cdiv style=\"display: flex; flex-direction: column; gap: 20px;\"\u003e\n \u003cp\u003e\u003cstrong\u003eTriton X-114 10%\u003c\/strong\u003e\u003c\/p\u003e\n \u003cdiv style=\"overflow-x: auto; max-width: 100%; margin-bottom: 20px;\"\u003e\n \u003ctable style=\"width: 500px; border-collapse: collapse;\"\u003e\n \u003ctbody\u003e\n \u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eCatalog number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e B2016309\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eLot number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch Dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eExpiration Date:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eAmount:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 10 mL\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eMolecular Weight or Concentration:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e ~537 (for n=7-8)\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eSupplied as:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Solution\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eApplications:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e a molecular tool for various biochemical applications\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eStorage:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e RT\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eKeywords:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 2-methyl-2-propenoic acid, polymer with 2-propenoic acid and N-octy-2-propenamide \/ alpha((1,1,3,3-tetramethylbutyl)phenyl)omega-hydroxypoly(oxy-1,2-ethanediyl) \/ charger E \/ ethoxylated octylphenol \/ ethylan CP \/ glycols, polyethylene, mono((1,1,3,3-tetramethylbutyl) phenyl)ether \/ igepal CA \/ igepal CA210 \/ igepal CA520 \/ neutronyx 622 \/ neutronyx 675 \/ nonidet P40 \/ nonion HS206 \/ nonion HS208 \/ NP-40 \/ octoxylol-9 \/ octyl phenol condensed with 20 moles ethylene oxide \/ octyl phenol condensed with 3 moles ethylene oxide \/ octyl phenol condensed with16 moles ethylene oxide \/ octyl phenol EO (16) \/ octyl phenol EO (3) \/ octylphenol polyethoxylate \/ octylphenoxypoly(ethoxyethanol) \/ octylphenoxypoly(ethyleneoxy)ethanol) \/ OP 1062 \/ OPE-3 \/ poly(ethylene oxide)octylphenyl ether \/ poly(ethylene oxide)tertiary-octylphenyl ether \/ poly(oxy-1,2-ethanediyl), alpha ((1,1,3,3-tetramethylbutyl)phenyl)-omega-hydroxy- \/ poly(oxyethylene)octylphenol ether \/ poly(oxyethylene)tertiary-octylphenol ether \/ poly(oxyethylene)tertiary-octylphenyl ether \/ polyethyleneglycol octylphenyl ether \/ polyethyleneglycol tertiary-octylphenyl ether \/ polyethyleneglycolmono((1,1,3,3-tetramethylbutyl)phenyl)ether \/ polyethyleneglycolmono(octylphenyl)ether \/ polyoxyethylenemono-tertiary-octylphenyl ether \/ secopal OP 20 \/ synperonic OP \/ synperonic OP 10 \/ T 45 \/ T 45,polyglycol \/ tertiary- octylphenoxypoly(ethyleneoxy)ethanol \/ tertiary-octylphenoxypoly(oxyethylene)ethanol \/ tertiary-octylphenoxypolyethoxyethanol,nonionic,surfactant \/ tert- octylphenoxypoly(ethoxyethanol) \/ triton X 114 \/ triton X 15 \/ triton X 207\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eGrade:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity \u0026gt;18 MΩ-cm) and are filtered through 0.22 um.\u003c\/td\u003e\n \u003c\/tr\u003e\n \u003c\/tbody\u003e\n \u003c\/table\u003e\n \u003c\/div\u003e\n\n \u003chr\u003e\n \u003ch4\u003eReferences\u003c\/h4\u003e\n \n \u003cul style=\"padding-left: 20px; margin: 0;\"\u003e\n \u003cli\u003eMagalhães PO, Lopes AM, Mazzola PG, Rangel-Yagui C, Penna TC, Pessoa A Jr. Methods of endotoxin removal from biological preparations: a review J Pharm Pharm Sci. 2007;10(3):388-404.\u003c\/li\u003e\n\u003cli\u003eRay SS, Chen SS, Nguyen NC, Nguyen HT, Dan NP, Thanh BX, Trang LT. Exploration of polyelectrolyte incorporated with Triton-X 114 surfactant based osmotic agent for forward osmosis desalination J Environ Manage. 2018 Mar 1;209:346-353.\u003c\/li\u003e\n\u003cli\u003eLi S, Cheng Y, Qin M, Chen S, Li P, Yang L. Exploring the utility of Au@PVP-polyamide-Triton X-114 for SERS tracking of extracellular senescence associated-beta-galactosidase activity Anal Methods. 2021 May 13;13(18):2087-2091.\u003c\/li\u003e\n\u003cli\u003eFilik H, Sener I, Cekiç SD, Kiliç E, Apak R. Spectrophotometric determination of paracetamol in urine with tetrahydroxycalix[4]arene as a coupling reagent and preconcentration with triton X-114 using cloud point extraction Chem Pharm Bull (Tokyo). 2006 Jun;54(6):891-6.\u003c\/li\u003e\n\u003cli\u003eSeth P, Willingham MC, Pastan I. Binding of adenovirus and its external proteins to Triton X-114. Dependence on pH J Biol Chem. 1985 Nov 25;260(27):14431-4.\u003c\/li\u003e\n\u003cli\u003eVachereau A. Transparency of nitrocellulose membranes with Triton X-114 Electrophoresis. 1989 Jul;10(7):524-7.\u003c\/li\u003e\n\u003cli\u003eSonesson A, Berglund M, Staxén I, Widell S. The characterization of plasma membrane-bound tubulin of cauliflower using Triton X-114 fractionation Plant Physiol. 1997 Nov;115(3):1001-7.\u003c\/li\u003e\n\u003cli\u003ePavić T, Gudelj I, Keser T, Pučić-Baković M, Gornik O. Enrichment of hydrophobic membrane proteins using Triton X-114 and subsequent analysis of their N-glycosylation Biochim Biophys Acta. 2016 Aug;1860(8):1710-5.\u003c\/li\u003e\n\u003cli\u003eDu K, Li J, Tian F, Chang YX. Non-ionic detergent Triton X-114 Based vortex- synchronized matrix solid-phase dispersion method for the simultaneous determination of six compounds with various polarities from Forsythiae Fructus by ultra high-performance liquid chromatography J Pharm Biomed Anal. 2018 Feb 20;150:59-66.\u003c\/li\u003e\n \u003c\/ul\u003e\n \u003c\/div\u003e\n \u003c\/div\u003e","brand":"Molecular Depot","offers":[{"title":"Default Title","offer_id":50482768347434,"sku":"BTS-B2016309","price":795.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0896\/1579\/4474\/files\/B2016309.png?v=1754943028"},{"product_id":"methanesulfonic-acid-highly-pure","title":"Methanesulfonic Acid (Highly Pure)","description":"\u003cdiv style=\"max-width: 1400px; margin: 0 auto; padding: 40px 20px; font-family: 'Open Sans', sans-serif; font-weight: 300; background: #fff; color: #333; font-size: 0.95rem; box-sizing: border-box;\"\u003e\n \u003cdiv style=\"display: flex; flex-direction: column; gap: 20px;\"\u003e\n \u003cp\u003e\u003cstrong\u003eMethanesulfonic Acid (Highly Pure)\u003c\/strong\u003e\u003c\/p\u003e\n \u003cdiv style=\"overflow-x: auto; max-width: 100%; margin-bottom: 20px;\"\u003e\n \u003ctable style=\"width: 500px; border-collapse: collapse;\"\u003e\n \u003ctbody\u003e\n \u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eCatalog number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e B2016267\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eLot number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch Dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eExpiration Date:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eAmount:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 1 mL\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eMolecular Weight or Concentration:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 96.11\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eSupplied as:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Liquid\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eApplications:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e a molecular tool for various biochemical applications\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eStorage:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e RT\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eKeywords:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Methanesulfonic Acid\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eGrade:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity \u0026gt;18 MΩ-cm) and are filtered through 0.22 um.\u003c\/td\u003e\n \u003c\/tr\u003e\n \u003c\/tbody\u003e\n \u003c\/table\u003e\n \u003c\/div\u003e\n\n \u003chr\u003e\n \u003ch4\u003eReferences\u003c\/h4\u003e\n \n \u003cul style=\"padding-left: 20px; margin: 0;\"\u003e\n \u003cli\u003eBritschgi J, Kersten W, Waldvogel SR, Schüth F. Electrochemically Initiated Synthesis of Methanesulfonic Acid Angew Chem Int Ed Engl. 2022 Oct 10;61(41):e202209591.\u003c\/li\u003e\n\u003cli\u003eChen J, Lane JR, Bates KH, Kjaergaard HG. Atmospheric Gas-Phase Formation of Methanesulfonic Acid Environ Sci Technol. 2023 Dec 19;57(50):21168-21177.\u003c\/li\u003e\n\u003cli\u003eElm J. Clusteromics II: Methanesulfonic Acid-Base Cluster Formation ACS Omega. 2021 Jun 23;6(26):17035-17044.\u003c\/li\u003e\n\u003cli\u003eWu N, Ning A, Liu L, Zu H, Liang D, Zhang X. Methanesulfonic acid and iodous acid nucleation: a novel mechanism for marine aerosols Phys Chem Chem Phys. 2023 Jun 28;25(25):16745-16752.\u003c\/li\u003e\n\u003cli\u003eHuff AK, Love N, Leopold KR. Microwave and Computational Study of Methanesulfonic Acid and Its Complex with Water J Phys Chem A. 2023 Apr 27;127(16):3658-3667.\u003c\/li\u003e\n\u003cli\u003eJohnson JS, Jen CN. Role of Methanesulfonic Acid in Sulfuric Acid-Amine and Ammonia New Particle Formation ACS Earth Space Chem. 2023 Mar 7;7(3):653-660.\u003c\/li\u003e\n\u003cli\u003eShen J, Scholz W, He XC, Zhou P, Marie G, Wang M, Marten R, Surdu M, Rörup B, Baalbaki R, Amorim A, Ataei F, Bell DM, Bertozzi B, Brasseur Z, Caudillo L, Chen D, Chu B, Dada L, Duplissy J, Finkenzeller H, Granzin M, Guida R, Heinritzi M, Hofbauer V, Iyer S, Kemppainen D, Kong W, Krechmer JE, Kürten A, Lamkaddam H, Lee CP, Lopez B, Mahfouz NGA, Manninen HE, Massabò D, Mauldin RL, Mentler B, Müller T, Pfeifer J, Philippov M, Piedehierro AA, Roldin P, Schobesberger S, Simon M, Stolzenburg D, Tham YJ, Tomé A, Umo NS, Wang D, Wang Y, Weber SK, Welti A, Wollesen de Jonge R, Wu Y, Zauner-Wieczorek M, Zust F, Baltensperger U, Curtius J, Flagan RC, Hansel A, Möhler O, Petäjä T, Volkamer R, Kulmala M, Lehtipalo K, Rissanen M, Kirkby J, El-Haddad I, Bianchi F, Sipilä M, Donahue NM, Worsnop DR. High Gas-Phase Methanesulfonic Acid Production in the OH-Initiated Oxidation of Dimethyl Sulfide at Low Temperatures Environ Sci Technol. 2022 Oct 4;56(19):13931-13944.\u003c\/li\u003e\n\u003cli\u003eRasmussen FR, Kubečka J, Elm J. Contribution of Methanesulfonic Acid to the Formation of Molecular Clusters in the Marine Atmosphere J Phys Chem A. 2022 Oct 13;126(40):7127-7136.\u003c\/li\u003e\n\u003cli\u003eEberlin AR, Eddleston MD, Frampton CS. Methanesulfonic acid salt forms of carbamazepine and 10,11-dihydrocarbamazepine Acta Crystallogr C. 2013 Nov;69(Pt 11):1260-6.\u003c\/li\u003e\n \u003c\/ul\u003e\n \u003c\/div\u003e\n \u003c\/div\u003e","brand":"Molecular Depot","offers":[{"title":"Default Title","offer_id":50482768380202,"sku":"BTS-B2016267","price":595.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0896\/1579\/4474\/files\/B2016267.png?v=1754943029"},{"product_id":"5-hydroxy-2-methylindole-highly-pure","title":"5-Hydroxy-2-methylindole (Highly Pure)","description":"\u003cdiv style=\"max-width: 1400px; margin: 0 auto; padding: 40px 20px; font-family: 'Open Sans', sans-serif; font-weight: 300; background: #fff; color: #333; font-size: 0.95rem; box-sizing: border-box;\"\u003e\n \u003cdiv style=\"display: flex; flex-direction: column; gap: 20px;\"\u003e\n \u003cp\u003e\u003cstrong\u003e5-Hydroxy-2-methylindole (Highly Pure)\u003c\/strong\u003e\u003c\/p\u003e\n \u003cdiv style=\"overflow-x: auto; max-width: 100%; margin-bottom: 20px;\"\u003e\n \u003ctable style=\"width: 500px; border-collapse: collapse;\"\u003e\n \u003ctbody\u003e\n \u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eCatalog number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e B2016273\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eLot number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch Dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eExpiration Date:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eAmount:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 250 mg\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eMolecular Weight or Concentration:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 147.18 g\/mol\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eSupplied as:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Powder\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eApplications:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e a molecular tool for various biochemical applications\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eStorage:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e -20°C\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eKeywords:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 5-Hydroxy-2-methylindole\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eGrade:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity \u0026gt;18 MΩ-cm) and are filtered through 0.22 um.\u003c\/td\u003e\n \u003c\/tr\u003e\n \u003c\/tbody\u003e\n \u003c\/table\u003e\n \u003c\/div\u003e\n\n \u003chr\u003e\n \u003ch4\u003eReferences\u003c\/h4\u003e\n \n \u003cul style=\"padding-left: 20px; margin: 0;\"\u003e\n \u003cli\u003eMulwad VV, Parmar HT, Mir AA. Synthesis of biologically active 1′-(2-oxo-2H-benzopyran-6-yl)- 5′-hydroxy-2′-methylindole-3′-amido-2″-phenyl-thiazolidene-4″-ones Acta Pol Pharm. 2011 Jan-Feb;68(1):49-55.\u003c\/li\u003e\n\u003cli\u003eBell MR, Oesterlin R, Beyler AL, Harding HR, Potts GO. Isomeric Mannich bases derived from ethyl 5-hydroxy-2-methylindole-3-carboxylate J Med Chem. 1967 Mar;10(2):264-6.\u003c\/li\u003e\n\u003cli\u003eThe MICAD Research Team. [(11)C]5-Hydroxy-2-(4-methyaminophenyl)benzofuran 2006 Oct 7 [updated 2006 Oct 16]. In: Molecular Imaging and Contrast Agent Database (MICAD) [Internet]. Bethesda (MD): National Center for Biotechnology Information (US); 2004–2013.\u003c\/li\u003e\n\u003cli\u003eBanskota AH, Stefanova R, Hui JPM, Berrué F, Achenbach JC, Ellis L. 9,10-Dihydro-5-hydroxy-2,3,6-trimethoxyphenanthrene-1,4-dione: a new dihydrophenanthrene from commercial cannabis and its effect on zebrafish larval behaviour Nat Prod Res. 2022 Jul;36(14):3553-3558.\u003c\/li\u003e\n\u003cli\u003eKim M, Truss M, Pagare PP, Essandoh MA, Zhang Y, Williams DA. Structure activity relationship exploration of 5-hydroxy-2-(3-phenylpropyl)chromones as a unique 5-HT(2B) receptor antagonist scaffold Bioorg Med Chem Lett. 2020 Nov 1;30(21):127511.\u003c\/li\u003e\n\u003cli\u003eTakeno M, Kitagawa S, Yamanaka J, Teramoto M, Tomita H, Shirai N, Itoh S, Hida S, Hayakawa K, Onozaki K, Takii T. 5-Hydroxy-2-methylpyridine Isolated from Cigarette Smoke Condensate Aggravates Collagen-Induced Arthritis in Mice Biol Pharm Bull. 2018;41(6):877-884.\u003c\/li\u003e\n\u003cli\u003eKanazawa S, Mizuno S, Yamauchi R, Nishimura N, Maeba I. Synthesis of 5-hydroxy-2-(beta-D-ribofuranosyl)pyran-4-one from a pyranulose glycoside Carbohydr Res. 1999 May 31;318(1-4):180-5.\u003c\/li\u003e\n\u003cli\u003eWilliams DA, Zaidi SA, Zhang Y. Synthesis and Characterization of 5-Hydroxy-2-(2-phenylethyl)chromone (5-HPEC) and Its Analogues as Non-nitrogenous 5-HT2B Ligands J Nat Prod. 2015 Aug 28;78(8):1859-67.\u003c\/li\u003e\n\u003cli\u003eLiao CH, Chen JJ, Lin JE, Liu CH, Tseng CP, Day YJ. 5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-3,7-dimethoxy-4H-chromen-4-one (MSF-2) suppresses fMLP-mediated respiratory burst in human neutrophils by inhibiting phosphatidylinositol 3-kinase activity J Cell Physiol. 2011 Jun;226(6):1519-30.\u003c\/li\u003e\n \u003c\/ul\u003e\n \u003c\/div\u003e\n \u003c\/div\u003e","brand":"Molecular Depot","offers":[{"title":"Default Title","offer_id":50482768675114,"sku":"BTS-B2016273","price":907.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0896\/1579\/4474\/files\/B2016273.png?v=1754943034"},{"product_id":"5-fluoroindole-highly-pure","title":"5-Fluoroindole (Highly Pure)","description":"\u003cdiv style=\"max-width: 1400px; margin: 0 auto; padding: 40px 20px; font-family: 'Open Sans', sans-serif; font-weight: 300; background: #fff; color: #333; font-size: 0.95rem; box-sizing: border-box;\"\u003e\n \u003cdiv style=\"display: flex; flex-direction: column; gap: 20px;\"\u003e\n \u003cp\u003e\u003cstrong\u003e5-Fluoroindole (Highly Pure)\u003c\/strong\u003e\u003c\/p\u003e\n \u003cdiv style=\"overflow-x: auto; max-width: 100%; margin-bottom: 20px;\"\u003e\n \u003ctable style=\"width: 500px; border-collapse: collapse;\"\u003e\n \u003ctbody\u003e\n \u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eCatalog number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e B2016271\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eLot number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch Dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eExpiration Date:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eAmount:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 25 g\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eMolecular Weight or Concentration:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 135.14 g\/mol\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eSupplied as:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Powder\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eApplications:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e a molecular tool for various biochemical applications\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eStorage:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e -20°C\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eKeywords:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 5-Fluoroindole\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eGrade:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity \u0026gt;18 MΩ-cm) and are filtered through 0.22 um.\u003c\/td\u003e\n \u003c\/tr\u003e\n \u003c\/tbody\u003e\n \u003c\/table\u003e\n \u003c\/div\u003e\n\n \u003chr\u003e\n \u003ch4\u003eReferences\u003c\/h4\u003e\n \n \u003cul style=\"padding-left: 20px; margin: 0;\"\u003e\n \u003cli\u003eFolkes LK, Greco O, Dachs GU, Stratford MR, Wardman P. 5-Fluoroindole-3-acetic acid: a prodrug activated by a peroxidase with potential for use in targeted cancer therapy Biochem Pharmacol. 2002 Jan 15;63(2):265-72.\u003c\/li\u003e\n\u003cli\u003eBarczak AJ, Zhao J, Pruitt KD, Last RL. 5-Fluoroindole resistance identifies tryptophan synthase beta subunit mutants in Arabidopsis thaliana Genetics. 1995 May;140(1):303-13.\u003c\/li\u003e\n\u003cli\u003eKamiński R, Przywara B, Gasior M, Kleinrok Z, Czuczwar SJ. Effect of 5-fluoroindole-2-carboxylic acid (an antagonist of the NMDA receptor-associated glycine site) on the anticonvulsive activity of conventional antiepileptic drugs J Neural Transm (Vienna). 1998;105(2-3):133-46.\u003c\/li\u003e\n\u003cli\u003eSethupathy S, Sathiyamoorthi E, Kim YG, Lee JH, Lee J. Antibiofilm and Antivirulence Properties of Indoles Against Serratia marcescens Front Microbiol. 2020 Oct 30;11:584812.\u003c\/li\u003e\n\u003cli\u003ePan B, Guo C, Liu D, Wüthrich K. Fluorine-19 labeling of the tryptophan residues in the G protein-coupled receptor NK1R using the 5-fluoroindole precursor in Pichia pastoris expression J Biomol NMR. 2024 Mar 30.\u003c\/li\u003e\n\u003cli\u003eAdoni P, Romanyuk A, Overton TW, Fernandez-Trillo P. Polymer-induced biofilms for enhanced biocatalysis Mater Horiz. 2022 Oct 3;9(10):2592-2602.\u003c\/li\u003e\n\u003cli\u003eWilke J, Wilke M, Brand C, Spiegel JD, Marian CM, Schmitt M. Modulation of the L(a)\/L(b) Mixing in an Indole Derivative: A Position-Dependent Study Using 4-, 5-, and 6-Fluoroindole J Phys Chem A. 2017 Mar 2;121(8):1597-1606.\u003c\/li\u003e\n\u003cli\u003eBrand C, Oeltermann O, Wilke M, Tatchen J, Schmitt M. Ground and electronically excited singlet-state structures of 5-fluoroindole deduced from rotationally resolved electronic spectroscopy and ab initio theory Chemphyschem. 2012 Sep 17;13(13):3134-8.\u003c\/li\u003e\n\u003cli\u003eCosottini L, Zineddu S, Massai L, Ghini V, Turano P. (19)F: A small probe for a giant protein J Inorg Biochem. 2023 Jul;244:112236.\u003c\/li\u003e\n \u003c\/ul\u003e\n \u003c\/div\u003e\n \u003c\/div\u003e","brand":"Molecular Depot","offers":[{"title":"Default Title","offer_id":50482769002794,"sku":"BTS-B2016271","price":1167.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0896\/1579\/4474\/files\/B2016271.png?v=1754943040"},{"product_id":"tectomer-2-tailed-highly-pure","title":"Tectomer 2-Tailed (Highly Pure)","description":"\u003cdiv style=\"max-width: 1400px; margin: 0 auto; padding: 40px 20px; font-family: 'Open Sans', sans-serif; font-weight: 300; background: #fff; color: #333; font-size: 0.95rem; box-sizing: border-box;\"\u003e\n \u003cdiv style=\"display: flex; flex-direction: column; gap: 20px;\"\u003e\n \u003cp\u003e\u003cstrong\u003eTectomer 2-Tailed (Highly Pure)\u003c\/strong\u003e\u003c\/p\u003e\n \u003cdiv style=\"overflow-x: auto; max-width: 100%; margin-bottom: 20px;\"\u003e\n \u003ctable style=\"width: 500px; border-collapse: collapse;\"\u003e\n \u003ctbody\u003e\n \u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eCatalog number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e B2016283\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eLot number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch Dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eExpiration Date:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eAmount:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 2 mg\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eMolecular Weight or Concentration:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e N\/A\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eSupplied as:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Powder\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eApplications:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e a molecular tool for various biochemical applications\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eStorage:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e -20°C\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eKeywords:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Tectomer 2-Tailed (Highly Pure)\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eGrade:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity \u0026gt;18 MΩ-cm) and are filtered through 0.22 um.\u003c\/td\u003e\n \u003c\/tr\u003e\n \u003c\/tbody\u003e\n \u003c\/table\u003e\n \u003c\/div\u003e\n\n \u003chr\u003e\n \u003ch4\u003eReferences\u003c\/h4\u003e\n \n \u003cul style=\"padding-left: 20px; margin: 0;\"\u003e\n \u003cli\u003eVilaval T, Sasinan W, Mayuree C, Chananun P, Somchai S. Effect of acupuncture on blood pressure control in hypertensive patients J Tradit Chin Med. 2019 Apr;39(2):246-250.\u003c\/li\u003e\n\u003cli\u003eBlackman AJ, Engasser WM, Krych AJ, Stuart MJ, Levy BA. Fibular head and tibial-based (2-Tailed) posterolateral corner reconstruction Sports Med Arthrosc Rev. 2015 Mar;23(1):44-50.\u003c\/li\u003e\n\u003cli\u003eMurata MA, Yamamoto LG. Single Versus Double-Sided Hypotheses and Probabilities Pediatr Emerg Care. 2021 Jul 1;37(7):386-388.\u003c\/li\u003e\n\u003cli\u003eSenthilnathan A, Larrondo J, De Souza B, Harris T, Eginli A, McMichael A. Topical Minoxidil Adherence in Patients With Alopecia J Drugs Dermatol. 2023 Mar 1;22(3):252-255.\u003c\/li\u003e\n\u003cli\u003eHönekopp J, Linden AH. Heterogeneity estimates in a biased world PLoS One. 2022 Feb 3;17(2):e0262809.\u003c\/li\u003e\n\u003cli\u003eKim H, Lee K, Lee YH, Park Y, Park Y, Yu Y, Park J, Noh S. The Effectiveness of a Mobile Phone-Based Physical Activity Program for Treating Depression, Stress, Psychological Well-Being, and Quality of Life Among Adults: Quantitative Study JMIR Mhealth Uhealth. 2023 Jun 26;11:e46286.\u003c\/li\u003e\n\u003cli\u003eCox MD, Trinidade A, Russell JS, Dornhoffer JL. Long-Term Hearing Results After Ossiculoplasty Otol Neurotol. 2017 Apr;38(4):510-515.\u003c\/li\u003e\n\u003cli\u003eNash DJ. An unusual two-tailed mouse Teratology. 1975 Oct;12(2):121-4.\u003c\/li\u003e\n\u003cli\u003eDeCoste R, McDonell LM, Uzans D, Molinari M, Huang WY. Comparing Pathology Report Quality Indicators in 2 Distinct Whipple Resection Specimen Protocols Pancreas. 2020 Jul;49(6):788-792.\u003c\/li\u003e\n \u003c\/ul\u003e\n \u003c\/div\u003e\n \u003c\/div\u003e","brand":"Molecular Depot","offers":[{"title":"Default Title","offer_id":50482769035562,"sku":"BTS-B2016283","price":795.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0896\/1579\/4474\/files\/B2016283.png?v=1754943040"},{"product_id":"5-methyl-dl-tryptophan-highly-pure","title":"5-Methyl-DL-tryptophan (Highly Pure)","description":"\u003cdiv style=\"max-width: 1400px; margin: 0 auto; padding: 40px 20px; font-family: 'Open Sans', sans-serif; font-weight: 300; background: #fff; color: #333; font-size: 0.95rem; box-sizing: border-box;\"\u003e\n \u003cdiv style=\"display: flex; flex-direction: column; gap: 20px;\"\u003e\n \u003cp\u003e\u003cstrong\u003e5-Methyl-DL-tryptophan (Highly Pure)\u003c\/strong\u003e\u003c\/p\u003e\n \u003cdiv style=\"overflow-x: auto; max-width: 100%; margin-bottom: 20px;\"\u003e\n \u003ctable style=\"width: 500px; border-collapse: collapse;\"\u003e\n \u003ctbody\u003e\n \u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eCatalog number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e B2016284\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eLot number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch Dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eExpiration Date:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eAmount:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 250 mg\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eMolecular Weight or Concentration:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 218.26 g\/mol\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eSupplied as:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Powder\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eApplications:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e a molecular tool for various biochemical applications\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eStorage:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 2-8°C\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eKeywords:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 5-Methyl-DL-tryptophan\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eGrade:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity \u0026gt;18 MΩ-cm) and are filtered through 0.22 um.\u003c\/td\u003e\n \u003c\/tr\u003e\n \u003c\/tbody\u003e\n \u003c\/table\u003e\n \u003c\/div\u003e\n\n \u003chr\u003e\n \u003ch4\u003eReferences\u003c\/h4\u003e\n \n \u003cul style=\"padding-left: 20px; margin: 0;\"\u003e\n \u003cli\u003eZou YF, Li CY, Fu YP, JiZe XP, Zhao YZ, Peng X, Wang JY, Yin ZQ, Li YP, Song X, Li LX, Zhao XH, Feng B, Huang C, Ye G, Tang HQ, Chen J, Li R, Chen XF, Tian ML. Angelica sinensis aboveground part polysaccharide and its metabolite 5-MT ameliorate colitis via modulating gut microbiota and TLR4\/MyD88\/NF-κB pathway Int J Biol Macromol. 2023 Jul 1;242(Pt 1):124689.\u003c\/li\u003e\n\u003cli\u003eHyde EI, Ramesh V, Frederick R, Roberts GC. NMR studies of the activation of the Escherichia coli trp repressor Eur J Biochem. 1991 Nov 1;201(3):569-79.\u003c\/li\u003e\n\u003cli\u003eRyu K, Nakamura S, Nakashima S, Matsuda H. One-pot enantioselective synthesis of (S)-spirobrassinin and non-natural (S)-methylspirobrassinin from amino acids using a turnip enzyme J Nat Med. 2021 Mar;75(2):308-318.\u003c\/li\u003e\n\u003cli\u003eFan A, Chen H, Wu R, Xu H, Li SM. A new member of the DMATS superfamily from Aspergillus niger catalyzes prenylations of both tyrosine and tryptophan derivatives Appl Microbiol Biotechnol. 2014 Dec;98(24):10119-29.\u003c\/li\u003e\n\u003cli\u003eSuzuki S, Hirahara T, Horinouchi S, Beppu T. Purification and properties of thermostable tryptophanase from an obligately symbiotic thermophile, Symbiobacterium thermophilum Agric Biol Chem. 1991 Dec;55(12):3059-66.\u003c\/li\u003e\n\u003cli\u003eMatsukawa T, Ishihara A, Iwamura H. Induction of anthranilate synthase activity by elicitors in oats Z Naturforsch C J Biosci. 2002 Jan-Feb;57(1-2):121-8.\u003c\/li\u003e\n\u003cli\u003eBertani G, Baresi L. Genetic transformation in the methanogen Methanococcus voltae PS J Bacteriol. 1987 Jun;169(6):2730-8.\u003c\/li\u003e\n\u003cli\u003eLester G. In vivo regulation of intermediate reactions in the pathway of tryptophan biosynthesis in Neurospora crassa J Bacteriol. 1968 Nov;96(5):1768-73.\u003c\/li\u003e\n\u003cli\u003eMorgan K, Leighton SP, Millar RP. Probing the GnRH receptor agonist binding site identifies methylated triptorelin as a new anti-proliferative agent J Mol Biochem. 2012 Jun 16;1(2):86-98.\u003c\/li\u003e\n \u003c\/ul\u003e\n \u003c\/div\u003e\n \u003c\/div\u003e","brand":"Molecular Depot","offers":[{"title":"Default Title","offer_id":50482769592618,"sku":"BTS-B2016284","price":995.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0896\/1579\/4474\/files\/B2016284.png?v=1754943047"},{"product_id":"x-d-fucopyranoside-highly-pure","title":"X-β-D-fucopyranoside (Highly Pure)","description":"\u003cdiv style=\"max-width: 1400px; margin: 0 auto; padding: 40px 20px; font-family: 'Open Sans', sans-serif; font-weight: 300; background: #fff; color: #333; font-size: 0.95rem; box-sizing: border-box;\"\u003e\n \u003cdiv style=\"display: flex; flex-direction: column; gap: 20px;\"\u003e\n \u003cp\u003e\u003cstrong\u003eX-β-D-fucopyranoside (Highly Pure)\u003c\/strong\u003e\u003c\/p\u003e\n \u003cdiv style=\"overflow-x: auto; max-width: 100%; margin-bottom: 20px;\"\u003e\n \u003ctable style=\"width: 500px; border-collapse: collapse;\"\u003e\n \u003ctbody\u003e\n \u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eCatalog number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e B2016222\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eLot number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch Dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eExpiration Date:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eAmount:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 25 mg\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eMolecular Weight or Concentration:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 392.64 g\/mol\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eSupplied as:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Powder\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eApplications:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e a molecular tool for various biochemical applications\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eStorage:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e -20°C\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eKeywords:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 5-Bromo-4-chloro-3-indoxyl-β-D-fucopyranoside\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eGrade:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity \u0026gt;18 MΩ-cm) and are filtered through 0.22 um.\u003c\/td\u003e\n \u003c\/tr\u003e\n \u003c\/tbody\u003e\n \u003c\/table\u003e\n \u003c\/div\u003e\n\n \u003chr\u003e\n \u003ch4\u003eReferences\u003c\/h4\u003e\n \n \u003cul style=\"padding-left: 20px; margin: 0;\"\u003e\n \u003cli\u003eJeyakumar M, Sathya S, Gandhi S, Tharra P, Suryanarayanan V, Singh SK, Baire B, Pandima Devi K. α-bisabolol β-D-fucopyranoside as a potential modulator of β-amyloid peptide induced neurotoxicity: An in vitro \u0026amp;in silico study Bioorg Chem. 2019 Jul;88:102935.\u003c\/li\u003e\n\u003cli\u003ePiochon M, Legault J, Gauthier C, Pichette A. Synthesis and cytotoxicity evaluation of natural alpha-bisabolol beta-D-fucopyranoside and analogues Phytochemistry. 2009 Jan;70(2):228-36.\u003c\/li\u003e\n\u003cli\u003eNguyen DH, Mitaine-Offer AC, Miyamoto T, Tanaka C, Bellaye PS, Collin B, Chambin O, Lacaille-Dubois MA. Steroidal glycosides from the Vietnamese cultivar Cordyline fruticosa “Fairchild red” Phytochemistry. 2021 Dec;192:112966.\u003c\/li\u003e\n\u003cli\u003eLiu Q, Lu JJ, Hong HJ, Yang Q, Wang Y, Chen XJ. Ophiopogon japonicus and its active compounds: A review of potential anticancer effects and underlying mechanisms Phytomedicine. 2023 May;113:154718.\u003c\/li\u003e\n\u003cli\u003eLi F, Wu ST, Qu MH, Wang YX, Ma CL, Yu BH, Wang GS. Triterpenoid saponins from the herb Hylomecon japonica Phytochemistry. 2021 Jan;181:112542.\u003c\/li\u003e\n\u003cli\u003eJeyakumar M, Jaya Balan D, Kiruthiga C, Jafni S, Pandima Devi K. α-bisabolol β-d-fucopyranoside (ABFP) ameliorates scopolamine-induced memory deficits through cholinesterase inhibition and attenuation of oxidative stress in zebrafish (Danio rerio) J Biochem Mol Toxicol. 2024 Jan;38(1):e23580.\u003c\/li\u003e\n\u003cli\u003eSakai T, Tanemura Y, Itoh S, Fujimoto Y. Dodecyl α-L-rhamnopyranosyl-(1→2)-β-D-fucopyranoside derivatives from the glandular trichome exudate of Erodium pelargoniflorum Chem Biodivers. 2013 Jun;10(6):1099-108.\u003c\/li\u003e\n\u003cli\u003eEsterly JR, Standen AC, Pearson B. The histochemical demonstration of intestinal beta-D-fucosidase with 5-bromo-4-chloroindole-3-yl-beta-D-fucopyranoside J Histochem Cytochem. 1967 Aug;15(8):470-4.\u003c\/li\u003e\n\u003cli\u003eHu Z, Jiang C, Qin M, Qi J, Yu B. [Determination of 25(R, S) ruscogenin 1-O-[beta-D-glucopyranosyl (1 –\u0026gt; 2)] [beta-D-xylopyranosyl (1 –\u0026gt; 3)] beta-D-fucopyranoside in Liriope muscari from different habitats and different harvest time by HPLC-ELSD] Zhongguo Zhong Yao Za Zhi. 2010 Oct;35(19):2508-10.\u003c\/li\u003e\n \u003c\/ul\u003e\n \u003c\/div\u003e\n \u003c\/div\u003e","brand":"Molecular Depot","offers":[{"title":"Default Title","offer_id":50503232782634,"sku":"BTS-B2016222","price":995.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0896\/1579\/4474\/files\/B2016222.png?v=1755359012"},{"product_id":"x-l-fucopyranoside-highly-pure","title":"X-α-L-fucopyranoside (Highly Pure)","description":"\u003cdiv style=\"max-width: 1400px; margin: 0 auto; padding: 40px 20px; font-family: 'Open Sans', sans-serif; font-weight: 300; background: #fff; color: #333; font-size: 0.95rem; box-sizing: border-box;\"\u003e\n \u003cdiv style=\"display: flex; flex-direction: column; gap: 20px;\"\u003e\n \u003cp\u003e\u003cstrong\u003eX-α-L-fucopyranoside (Highly Pure)\u003c\/strong\u003e\u003c\/p\u003e\n \u003cdiv style=\"overflow-x: auto; max-width: 100%; margin-bottom: 20px;\"\u003e\n \u003ctable style=\"width: 500px; border-collapse: collapse;\"\u003e\n \u003ctbody\u003e\n \u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eCatalog number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e B2016254\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eLot number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch Dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eExpiration Date:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eAmount:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 50 mg\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eMolecular Weight or Concentration:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 392.64 g\/mol\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eSupplied as:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Powder\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eApplications:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e a molecular tool for various biochemical applications\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eStorage:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e -20°C\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eKeywords:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 5-Bromo-4-chloro-3-indoxyl-α-L-fucopyranoside; X-alpha-L-Fucoside\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eGrade:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity \u0026gt;18 MΩ-cm) and are filtered through 0.22 um.\u003c\/td\u003e\n \u003c\/tr\u003e\n \u003c\/tbody\u003e\n \u003c\/table\u003e\n \u003c\/div\u003e\n\n \u003chr\u003e\n \u003ch4\u003eReferences\u003c\/h4\u003e\n \n \u003cul style=\"padding-left: 20px; margin: 0;\"\u003e\n \u003cli\u003eJančaříková G, Herczeg M, Fujdiarová E, Houser J, Kövér KE, Borbás A, Wimmerová M, Csávás M. Synthesis of α-l-Fucopyranoside-Presenting Glycoclusters and Investigation of Their Interaction with Photorhabdus asymbiotica Lectin (PHL) Chemistry. 2018 Mar 15;24(16):4055-4068.\u003c\/li\u003e\n\u003cli\u003eGu G, Du Y, Hu H, Jin C. Synthesis of 2-chloro-4-nitrophenyl alpha-L-fucopyranoside: a substrate for alpha-L-fucosidase (AFU) Carbohydr Res. 2003 Jul 22;338(15):1603-7.\u003c\/li\u003e\n\u003cli\u003eJain RK, Matta KL. Synthesis of the sodium salts of methyl 2-O-alpha-L-fucopyranosyl-alpha-L-fucopyranoside 3- and 4-sulfate Carbohydr Res. 1990 Dec 15;208:51-8.\u003c\/li\u003e\n\u003cli\u003ePerrella NN, Fuzita FJ, Moreti R, Verhaert PDEM, Lopes AR. First characterization of fucosidases in spiders Arch Insect Biochem Physiol. 2018 Jul;98(3):e21462.\u003c\/li\u003e\n\u003cli\u003eDejter-Juszynski M, Flowers HM. Synthesis of 4-O-alpha-L-fucopyranosyl-L-fucose and methyl 4-O-beta-L-fucopyranosyl-alpha-L-fucopyranoside Carbohydr Res. 1975 May;41:308-12.\u003c\/li\u003e\n\u003cli\u003eJain RK, Matta KL. Synthesis of methyl 2-O-(sodium alpha-L-fucopyranosyl 3- and 4-sulfate)-alpha-L-fucopyranoside Carbohydr Res. 1990 Dec 15;208:280-6.\u003c\/li\u003e\n\u003cli\u003eGrootaert H, Van Landuyt L, Hulpiau P, Callewaert N. Functional exploration of the GH29 fucosidase family Glycobiology. 2020 Aug 20;30(9):735-745.\u003c\/li\u003e\n\u003cli\u003eZhang Z, Li Y, Wu M, Gao Z, Wu B, He B. Identification and Characterization of a Novel α-L-Fucosidase from Enterococcus gallinarum and Its Application for Production of 2′-Fucosyllactose Int J Mol Sci. 2023 Jul 17;24(14):11555.\u003c\/li\u003e\n\u003cli\u003eBenesová E, Lipovová P, Dvoráková H, Králová B. α-L-fucosidase from Paenibacillus thiaminolyticus: its hydrolytic and transglycosylation abilities Glycobiology. 2013 Sep;23(9):1052-65.\u003c\/li\u003e\n \u003c\/ul\u003e\n \u003c\/div\u003e\n \u003c\/div\u003e","brand":"Molecular Depot","offers":[{"title":"Default Title","offer_id":50503232880938,"sku":"BTS-B2016254","price":1167.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0896\/1579\/4474\/files\/B2016254.png?v=1755359016"},{"product_id":"5-fluoro-2-nitrotoluene-highly-pure","title":"5-Fluoro-2-nitrotoluene (Highly Pure)","description":"\u003cdiv style=\"max-width: 1400px; margin: 0 auto; padding: 40px 20px; font-family: 'Open Sans', sans-serif; font-weight: 300; background: #fff; color: #333; font-size: 0.95rem; box-sizing: border-box;\"\u003e\n \u003cdiv style=\"display: flex; flex-direction: column; gap: 20px;\"\u003e\n \u003cp\u003e\u003cstrong\u003e5-Fluoro-2-nitrotoluene (Highly Pure)\u003c\/strong\u003e\u003c\/p\u003e\n \u003cdiv style=\"overflow-x: auto; max-width: 100%; margin-bottom: 20px;\"\u003e\n \u003ctable style=\"width: 500px; border-collapse: collapse;\"\u003e\n \u003ctbody\u003e\n \u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eCatalog number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e B2016214\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eLot number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch Dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eExpiration Date:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eAmount:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 100 g\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eMolecular Weight or Concentration:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 155.13 g\/mol\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eSupplied as:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Powder\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eApplications:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e a molecular tool for various biochemical applications\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eStorage:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e RT\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eKeywords:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 5-Fluoro-2-nitrotoluene\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eGrade:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity \u0026gt;18 MΩ-cm) and are filtered through 0.22 um.\u003c\/td\u003e\n \u003c\/tr\u003e\n \u003c\/tbody\u003e\n \u003c\/table\u003e\n \u003c\/div\u003e\n\n \u003chr\u003e\n \u003ch4\u003eReferences\u003c\/h4\u003e\n \n \u003cul style=\"padding-left: 20px; margin: 0;\"\u003e\n \u003cli\u003eLeung K. N-(5-Fluoro-2-phenoxyphenyl)-N-(2-[(18)F]fluoroethyl-5-methoxybenzyl)acetamide 2006 Mar 10 [updated 2008 Mar 27]. In: Molecular Imaging and Contrast Agent Database (MICAD) [Internet]. Bethesda (MD): National Center for Biotechnology Information (US); 2004–2013.\u003c\/li\u003e\n\u003cli\u003eLeung K. N-(5-Fluoro-2-phenoxyphenyl)-N-(2-[(131)I]iodo-5-methoxybenzyl)acetamide 2007 Aug 6 [updated 2007 Sep 12]. In: Molecular Imaging and Contrast Agent Database (MICAD) [Internet]. Bethesda (MD): National Center for Biotechnology Information (US); 2004–2013.\u003c\/li\u003e\n\u003cli\u003eLi W, Yin X, Schneller SW. 5′-Fluoro-5′-deoxyaristeromycin Bioorg Med Chem Lett. 2008 Jan 1;18(1):220-2.\u003c\/li\u003e\n\u003cli\u003eLaxio Arenas J, Retailleau P, Gillet JM, Ghermani NE, Ongeri S, Crousse B. 5-Fluoro-1,2,3-triazole motif in peptides and its electronic properties Org Biomol Chem. 2022 Nov 9;20(43):8410-8414.\u003c\/li\u003e\n\u003cli\u003eCao S, Zhang Z, Creaven PJ, Rustum YM. 5-Fluoro-2′-deoxyuridine: role of schedule in its therapeutic efficacy Adv Exp Med Biol. 1993;339:1-8; discussion 21.\u003c\/li\u003e\n\u003cli\u003eSolodinin A, Gautrais A, Ollivier S, Yan H. 5-Fluoro-2′-deoxycytidine as a Probe for the Study of B\/Z-DNA Transition by (19)F NMR Spectroscopy ACS Omega. 2019 Nov 15;4(22):19716-19722.\u003c\/li\u003e\n\u003cli\u003eCapecitabine 2021 Aug 16. Drugs and Lactation Database (LactMed®) [Internet]. Bethesda (MD): National Institute of Child Health and Human Development; 2006–.\u003c\/li\u003e\n\u003cli\u003eFluorouracil 2021 May 17. Drugs and Lactation Database (LactMed®) [Internet]. Bethesda (MD): National Institute of Child Health and Human Development; 2006–.\u003c\/li\u003e\n\u003cli\u003eJiang Y, Wu K, Cui D, Zhou W. 2-Chloro-5-fluoro-6-methyl-N-o-tolyl-pyrimidin-4-amine Acta Crystallogr Sect E Struct Rep Online. 2013 Apr 5;69(Pt 5):o626.\u003c\/li\u003e\n \u003c\/ul\u003e\n \u003c\/div\u003e\n \u003c\/div\u003e","brand":"Molecular Depot","offers":[{"title":"Default Title","offer_id":50503234257194,"sku":"BTS-B2016214","price":907.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0896\/1579\/4474\/files\/B2016214.png?v=1755359079"},{"product_id":"5-cyanoindole-highly-pure","title":"5-Cyanoindole (Highly Pure)","description":"\u003cdiv style=\"max-width: 1400px; margin: 0 auto; padding: 40px 20px; font-family: 'Open Sans', sans-serif; font-weight: 300; background: #fff; color: #333; font-size: 0.95rem; box-sizing: border-box;\"\u003e\n \u003cdiv style=\"display: flex; flex-direction: column; gap: 20px;\"\u003e\n \u003cp\u003e\u003cstrong\u003e5-Cyanoindole (Highly Pure)\u003c\/strong\u003e\u003c\/p\u003e\n \u003cdiv style=\"overflow-x: auto; max-width: 100%; margin-bottom: 20px;\"\u003e\n \u003ctable style=\"width: 500px; border-collapse: collapse;\"\u003e\n \u003ctbody\u003e\n \u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eCatalog number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e B2016217\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eLot number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch Dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eExpiration Date:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eAmount:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 5 g\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eMolecular Weight or Concentration:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 142.16 g\/mol\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eSupplied as:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Powder\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eApplications:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e a molecular tool for various biochemical applications\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eStorage:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e -20°C\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eKeywords:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Indole-5-cyanonitrile\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eGrade:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity \u0026gt;18 MΩ-cm) and are filtered through 0.22 um.\u003c\/td\u003e\n \u003c\/tr\u003e\n \u003c\/tbody\u003e\n \u003c\/table\u003e\n \u003c\/div\u003e\n\n \u003chr\u003e\n \u003ch4\u003eReferences\u003c\/h4\u003e\n \n \u003cul style=\"padding-left: 20px; margin: 0;\"\u003e\n \u003cli\u003eYokogawa D. Time-dependent density functional theory (TD-DFT) coupled with reference interaction site model self-consistent field explicitly including spatial electron density distribution (RISM-SCF-SEDD) J Chem Phys. 2016 Sep 7;145(9):094101.\u003c\/li\u003e\n\u003cli\u003eWaegele MM, Gai F. Computational Modeling of the Nitrile Stretching Vibration of 5-Cyanoindole in Water J Phys Chem Lett. 2010 Feb 1;1(4):781-786.\u003c\/li\u003e\n\u003cli\u003eOeltermann O, Brand C, Engels B, Tatchen J, Schmitt M. The structure of 5-cyanoindole in the ground and the lowest electronically excited singlet states, deduced from rotationally resolved electronic spectroscopy and ab initio theory Phys Chem Chem Phys. 2012 Aug 7;14(29):10266-70.\u003c\/li\u003e\n\u003cli\u003eYang Y, Liu J, Feng RR, Zhang W, Gai F. C≡N Stretching Frequency as a Convenient Reporter of Charge Separation in Molecular Systems J Phys Chem B. 2023 Aug 10;127(31):6999-7003.\u003c\/li\u003e\n\u003cli\u003eStuhlmann B, Gräßle A, Schmitt M. Determination of the geometry change of 5-cyanoindole upon electronic excitation from a combined Franck-Condon\/rotational constants fit Phys Chem Chem Phys. 2014 Jan 21;16(3):899-905.\u003c\/li\u003e\n\u003cli\u003eMarkiewicz BN, Mukherjee D, Troxler T, Gai F. Utility of 5-Cyanotryptophan Fluorescence as a Sensitive Probe of Protein Hydration J Phys Chem B. 2016 Feb 11;120(5):936-44.\u003c\/li\u003e\n\u003cli\u003eTalbi H, Billaud D, Louarn G, Pron A. UV-vis and Raman spectroelectrochemical investigation of the redox behavior of poly(5-cyanoindole) in acidic aqueous solutions Spectrochim Acta A Mol Biomol Spectrosc. 2000 Mar;56(4):717-28.\u003c\/li\u003e\n\u003cli\u003eHebestreit ML, Schneider M, Lartian H, Betz V, Heinrich M, Lindic M, Choi MY, Schmitt M. Structures, dipole moments and excited state lifetime of isolated 4-cyanoindole in its ground and lowest electronically excited singlet states Phys Chem Chem Phys. 2019 Jul 10;21(27):14766-14774.\u003c\/li\u003e\n\u003cli\u003eLakhdar S, Westermaier M, Terrier F, Goumont R, Boubaker T, Ofial AR, Mayr H. Nucleophilic reactivities of indoles J Org Chem. 2006 Nov 24;71(24):9088-95.\u003c\/li\u003e\n \u003c\/ul\u003e\n \u003c\/div\u003e\n \u003c\/div\u003e","brand":"Molecular Depot","offers":[{"title":"Default Title","offer_id":50503234289962,"sku":"BTS-B2016217","price":907.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0896\/1579\/4474\/files\/B2016217.png?v=1755359083"},{"product_id":"5-bromoindole-highly-pure","title":"5-Bromoindole (Highly Pure)","description":"\u003cdiv style=\"max-width: 1400px; margin: 0 auto; padding: 40px 20px; font-family: 'Open Sans', sans-serif; font-weight: 300; background: #fff; color: #333; font-size: 0.95rem; box-sizing: border-box;\"\u003e\n \u003cdiv style=\"display: flex; flex-direction: column; gap: 20px;\"\u003e\n \u003cp\u003e\u003cstrong\u003e5-Bromoindole (Highly Pure)\u003c\/strong\u003e\u003c\/p\u003e\n \u003cdiv style=\"overflow-x: auto; max-width: 100%; margin-bottom: 20px;\"\u003e\n \u003ctable style=\"width: 500px; border-collapse: collapse;\"\u003e\n \u003ctbody\u003e\n \u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eCatalog number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e B2016226\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eLot number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch Dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eExpiration Date:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eAmount:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 50 g\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eMolecular Weight or Concentration:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 196.05 g\/mol\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eSupplied as:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Powder\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eApplications:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e a molecular tool for various biochemical applications\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eStorage:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 2-8°C\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eKeywords:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 5-Bromoindole 99.5+%\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eGrade:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity \u0026gt;18 MΩ-cm) and are filtered through 0.22 um.\u003c\/td\u003e\n \u003c\/tr\u003e\n \u003c\/tbody\u003e\n \u003c\/table\u003e\n \u003c\/div\u003e\n\n \u003chr\u003e\n \u003ch4\u003eReferences\u003c\/h4\u003e\n \n \u003cul style=\"padding-left: 20px; margin: 0;\"\u003e\n \u003cli\u003eHassan OM, Kubba A, Tahtamouni LH. Novel 5-bromoindole-2-carboxylic Acid Derivatives as EGFR Inhibitors: Synthesis, Docking Study, and Structure Activity Relationship Anticancer Agents Med Chem. 2023;23(11):1336-1348.\u003c\/li\u003e\n\u003cli\u003eButler-Fernández KM, Ramos Z, Francis-Malavé AM, Bloom J, Dharmawardhane S, Hernández E. Synthesis, Anti-Cancer and Anti-Migratory Evaluation of 3,6-Dibromocarbazole and 5-Bromoindole Derivatives Molecules. 2019 Jul 24;24(15):2686.\u003c\/li\u003e\n\u003cli\u003eTasdemir D, Bugni TS, Mangalindan GC, Concepción GP, Harper MK, Ireland CM. Cytotoxic bromoindole derivatives and terpenes from the Philippine marine sponge Smenospongia sp Z Naturforsch C J Biosci. 2002 Sep-Oct;57(9-10):914-22.\u003c\/li\u003e\n\u003cli\u003eTupper J, Stratford MR, Hill S, Tozer GM, Dachs GU. In vivo characterization of horseradish peroxidase with indole-3-acetic acid and 5-bromoindole-3-acetic acid for gene therapy of cancer Cancer Gene Ther. 2010 Jun;17(6):420-8.\u003c\/li\u003e\n\u003cli\u003eSuárez-Castillo OR, Beiza-Granados L, Meléndez-Rodríguez M, Alvarez-Hernández A, Morales-Ríos MS, Joseph-Nathan P. Synthesis of bromoindole alkaloids from Laurencia brongniartii J Nat Prod. 2006 Nov;69(11):1596-600.\u003c\/li\u003e\n\u003cli\u003eBengtsson C, Gravenfors Y. Rapid Construction of a Chloromethyl-Substituted Duocarmycin-like Prodrug Molecules. 2023 Jun 16;28(12):4818.\u003c\/li\u003e\n\u003cli\u003eMphahlele MJ, Parbhoo N. Synthesis, Evaluation of Cytotoxicity and Molecular Docking Studies of the 7-Acetamido Substituted 2-Aryl-5-bromo-3-trifluoroacetylindoles as Potential Inhibitors of Tubulin Polymerization Pharmaceuticals (Basel). 2018 Jun 11;11(2):59.\u003c\/li\u003e\n\u003cli\u003eMédici R, Garaycoechea JI, Dettorre LA, Iribarren AM, Lewkowicz ES. Biocatalysed halogenation of nucleobase analogues Biotechnol Lett. 2011 Oct;33(10):1999-2003.\u003c\/li\u003e\n\u003cli\u003eManoharan RK, Raorane CJ, Ishaque F, Ahn YH. Antimicrobial photodynamic inactivation of wastewater microorganisms by halogenated indole derivative capped zinc oxide Environ Res. 2022 Nov;214(Pt 3):113905.\u003c\/li\u003e\n \u003c\/ul\u003e\n \u003c\/div\u003e\n \u003c\/div\u003e","brand":"Molecular Depot","offers":[{"title":"Default Title","offer_id":50503234322730,"sku":"BTS-B2016226","price":907.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0896\/1579\/4474\/files\/B2016226.png?v=1755359084"},{"product_id":"5-nitro-dl-tryptophan-highly-pure","title":"5-Nitro-DL-tryptophan (Highly Pure)","description":"\u003cdiv style=\"max-width: 1400px; margin: 0 auto; padding: 40px 20px; font-family: 'Open Sans', sans-serif; font-weight: 300; background: #fff; color: #333; font-size: 0.95rem; box-sizing: border-box;\"\u003e\n \u003cdiv style=\"display: flex; flex-direction: column; gap: 20px;\"\u003e\n \u003cp\u003e\u003cstrong\u003e5-Nitro-DL-tryptophan (Highly Pure)\u003c\/strong\u003e\u003c\/p\u003e\n \u003cdiv style=\"overflow-x: auto; max-width: 100%; margin-bottom: 20px;\"\u003e\n \u003ctable style=\"width: 500px; border-collapse: collapse;\"\u003e\n \u003ctbody\u003e\n \u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eCatalog number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e B2016218\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eLot number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch Dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eExpiration Date:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eAmount:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 250 mg\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eMolecular Weight or Concentration:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 249.23 g\/mol\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eSupplied as:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Solution When Dissolved\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eApplications:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e a molecular tool for various biochemical applications\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eStorage:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 2-8°C\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eKeywords:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e DL-2-Amino-3-(5-nitroindolyl)propionic acid; H-5-Nitro-DL-Trp-OH\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eGrade:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity \u0026gt;18 MΩ-cm) and are filtered through 0.22 um.\u003c\/td\u003e\n \u003c\/tr\u003e\n \u003c\/tbody\u003e\n \u003c\/table\u003e\n \u003c\/div\u003e\n\n \u003chr\u003e\n \u003ch4\u003eReferences\u003c\/h4\u003e\n \n \u003cul style=\"padding-left: 20px; margin: 0;\"\u003e\n \u003cli\u003eChoi JS, Kim CS, Berdis A. Inhibition of Translesion DNA Synthesis as a Novel Therapeutic Strategy to Treat Brain Cancer Cancer Res. 2018 Feb 15;78(4):1083-1096.\u003c\/li\u003e\n\u003cli\u003eChoi JS, Berdis A. Artificial Nucleosides as Diagnostic Probes to Measure Translesion DNA Synthesis Methods Mol Biol. 2019;1973:237-249.\u003c\/li\u003e\n\u003cli\u003eMotea EA, Lee I, Berdis AJ. A non-natural nucleoside with combined therapeutic and diagnostic activities against leukemia ACS Chem Biol. 2012 Jun 15;7(6):988-98.\u003c\/li\u003e\n\u003cli\u003eMotea EA, Lee I, Berdis AJ. Development of a ‘clickable’ non-natural nucleotide to visualize the replication of non-instructional DNA lesions Nucleic Acids Res. 2012 Mar;40(5):2357-67.\u003c\/li\u003e\n\u003cli\u003eReineks EZ, Berdis AJ. Evaluating the contribution of base stacking during translesion DNA replication Biochemistry. 2004 Jan 20;43(2):393-404.\u003c\/li\u003e\n\u003cli\u003eAhmad MF, Wan Q, Jha S, Motea E, Berdis A, Dealwis C. Evaluating the therapeutic potential of a non-natural nucleotide that inhibits human ribonucleotide reductase Mol Cancer Ther. 2012 Oct;11(10):2077-86.\u003c\/li\u003e\n\u003cli\u003eWu X, Ma X, Zhong Y, Chen W, Xu M, Zhang H, Wang L, Tu X, Han Z, Zhao W, Wu Z, Moschos SJ, Li Z. Development of [(18)F]F-5-OMe-Tryptophans through Photoredox Radiofluorination: A New Method to Access Tryptophan-Based PET Agents J Med Chem. 2023 Mar 9;66(5):3262-3272.\u003c\/li\u003e\n\u003cli\u003eShirmovsky SE, Chizhov AV. Modeling of the entangled states transfer processes in microtubule tryptophan system Biosystems. 2023 Sep;231:104967.\u003c\/li\u003e\n\u003cli\u003eZou Y, Yu L, Fang X, Zheng Y, Yang Y, Wang C. Position-coded multivalent peptide-peptide interactions revealed by tryptophan-scanning mutagenesis J Pept Sci. 2020 Sep;26(9):e3273.\u003c\/li\u003e\n \u003c\/ul\u003e\n \u003c\/div\u003e\n \u003c\/div\u003e","brand":"Molecular Depot","offers":[{"title":"Default Title","offer_id":50503234355498,"sku":"BTS-B2016218","price":795.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0896\/1579\/4474\/files\/B2016218.png?v=1755359084"},{"product_id":"5-fluoro-l-tryptophan-monohydrate-highly-pure","title":"5-Fluoro-L-tryptophan Monohydrate (Highly Pure)","description":"\u003cdiv style=\"max-width: 1400px; margin: 0 auto; padding: 40px 20px; font-family: 'Open Sans', sans-serif; font-weight: 300; background: #fff; color: #333; font-size: 0.95rem; box-sizing: border-box;\"\u003e\n \u003cdiv style=\"display: flex; flex-direction: column; gap: 20px;\"\u003e\n \u003cp\u003e\u003cstrong\u003e5-Fluoro-L-tryptophan Monohydrate (Highly Pure)\u003c\/strong\u003e\u003c\/p\u003e\n \u003cdiv style=\"overflow-x: auto; max-width: 100%; margin-bottom: 20px;\"\u003e\n \u003ctable style=\"width: 500px; border-collapse: collapse;\"\u003e\n \u003ctbody\u003e\n \u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eCatalog number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e B2016227\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eLot number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch Dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eExpiration Date:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eAmount:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 100 mg\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eMolecular Weight or Concentration:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 240.24 g\/mol\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eSupplied as:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Powder\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eApplications:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e a molecular tool for various biochemical applications\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eStorage:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e -20°C\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eKeywords:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e H-5-Fluoro-Trp-OH\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eGrade:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity \u0026gt;18 MΩ-cm) and are filtered through 0.22 um.\u003c\/td\u003e\n \u003c\/tr\u003e\n \u003c\/tbody\u003e\n \u003c\/table\u003e\n \u003c\/div\u003e\n\n \u003chr\u003e\n \u003ch4\u003eReferences\u003c\/h4\u003e\n \n \u003cul style=\"padding-left: 20px; margin: 0;\"\u003e\n \u003cli\u003eEriksson O, Selvaraju R, Borg B, Asplund V, Estrada S, Antoni G. 5-Fluoro-[β-¹¹C]-L-tryptophan is a functional analogue of 5-hydroxy-[β-¹¹C]-L-tryptophan in vitro but not in vivo Nucl Med Biol. 2013 May;40(4):567-75.\u003c\/li\u003e\n\u003cli\u003eFerrer L, Elsaraf M, Mindt M, Wendisch VF. l-Serine Biosensor-Controlled Fermentative Production of l-Tryptophan Derivatives by Corynebacterium glutamicum Biology (Basel). 2022 May 13;11(5):744.\u003c\/li\u003e\n\u003cli\u003eTang T, Gill HS, Ogasawara A, Tinianow JN, Vanderbilt AN, Williams SP, Hatzivassiliou G, White S, Sandoval W, DeMent K, Wong M, Marik J. Preparation and evaluation of L- and D-5-[(18)F]fluorotryptophan as PET imaging probes for indoleamine and tryptophan 2,3-dioxygenases Nucl Med Biol. 2017 Aug;51:10-17.\u003c\/li\u003e\n\u003cli\u003ePfefferkorn CM, Lee JC. 5-fluoro-D,L-tryptophan as a dual NMR and fluorescent probe of α-synuclein Methods Mol Biol. 2012;895:197-209.\u003c\/li\u003e\n\u003cli\u003eMiles EW, Phillips RS, Yeh HJ, Cohen LA. Isomerization of (3S)-2,3-dihydro-5-fluoro-L-tryptophan and of 5-fluoro-L-tryptophan catalyzed by tryptophan synthase: studies using fluorine-19 nuclear magnetic resonance and difference spectroscopy Biochemistry. 1986 Jul 29;25(15):4240-9.\u003c\/li\u003e\n\u003cli\u003eAymard N, Honore P, Carbuccia I. Determination of 5-hydroxytryptamine and tryptophan by liquid chromatography in whole blood. Its interest for the exploration of mental disorders Prog Neuropsychopharmacol Biol Psychiatry. 1994 Jan;18(1):77-86.\u003c\/li\u003e\n\u003cli\u003ePhillips RS. Reactions of O-acyl-L-serines with tryptophanase, tyrosine phenol-lyase, and tryptophan synthase Arch Biochem Biophys. 1987 Jul;256(1):302-10.\u003c\/li\u003e\n\u003cli\u003eRosenfeld H, Feigelson P. Product induction in Pseudomonas acidovorans of a permease system which transports L-tryptophan J Bacteriol. 1969 Feb;97(2):705-14.\u003c\/li\u003e\n\u003cli\u003eBrady FO, Feigelson P. The oxygenated complexes of the two catalytically active oxidation-reduction states of L-tryptophan-2,3-dioxygenase J Biol Chem. 1975 Jul 10;250(13):5041-8.\u003c\/li\u003e\n \u003c\/ul\u003e\n \u003c\/div\u003e\n \u003c\/div\u003e","brand":"Molecular Depot","offers":[{"title":"Default Title","offer_id":50503234388266,"sku":"BTS-B2016227","price":1167.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0896\/1579\/4474\/files\/B2016227.png?v=1755359085"},{"product_id":"5-chloro-dl-tryptophan-highly-pure","title":"5-Chloro-DL-tryptophan (Highly Pure)","description":"\u003cdiv style=\"max-width: 1400px; margin: 0 auto; padding: 40px 20px; font-family: 'Open Sans', sans-serif; font-weight: 300; background: #fff; color: #333; font-size: 0.95rem; box-sizing: border-box;\"\u003e\n \u003cdiv style=\"display: flex; flex-direction: column; gap: 20px;\"\u003e\n \u003cp\u003e\u003cstrong\u003e5-Chloro-DL-tryptophan (Highly Pure)\u003c\/strong\u003e\u003c\/p\u003e\n \u003cdiv style=\"overflow-x: auto; max-width: 100%; margin-bottom: 20px;\"\u003e\n \u003ctable style=\"width: 500px; border-collapse: collapse;\"\u003e\n \u003ctbody\u003e\n \u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eCatalog number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e B2016229\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eLot number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch Dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eExpiration Date:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eAmount:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 250 mg\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eMolecular Weight or Concentration:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 238.68 g\/mol\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eSupplied as:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Powder\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eApplications:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e a molecular tool for various biochemical applications\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eStorage:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e -20°C\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eKeywords:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e DL-2-Amino-3-(5-chloroindolyl)propionic acid; H-5-Chloro-DL-Trp-OH\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eGrade:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity \u0026gt;18 MΩ-cm) and are filtered through 0.22 um.\u003c\/td\u003e\n \u003c\/tr\u003e\n \u003c\/tbody\u003e\n \u003c\/table\u003e\n \u003c\/div\u003e\n\n \u003chr\u003e\n \u003ch4\u003eReferences\u003c\/h4\u003e\n \n \u003cul style=\"padding-left: 20px; margin: 0;\"\u003e\n \u003cli\u003eKnight CG. A quenched fluorescent substrate for thimet peptidase containing a new fluorescent amino acid, DL-2-amino-3-(7-methoxy-4-coumaryl)propionic acid Biochem J. 1991 Feb 15;274 ( Pt 1)(Pt 1):45-8.\u003c\/li\u003e\n\u003cli\u003eLaber B, Gerbling KP, Harde C, Neff KH, Nordhoff E, Pohlenz HD. Mechanisms of interaction of Escherichia coli threonine synthase with substrates and inhibitors Biochemistry. 1994 Mar 22;33(11):3413-23.\u003c\/li\u003e\n\u003cli\u003eOkada D. Two pathways of cyclic GMP production through glutamate receptor-mediated nitric oxide synthesis J Neurochem. 1992 Oct;59(4):1203-10.\u003c\/li\u003e\n\u003cli\u003eLaabich A, Cooper NG. Regulation of calcium\/calmodulin-dependent protein kinase II in the adult rat retina is mediated by ionotropic glutamate receptors Exp Eye Res. 1999 Jun;68(6):703-13.\u003c\/li\u003e\n\u003cli\u003eHoller T, Cappel E, Klein J, Löffelholz K. Glutamate activates phospholipase D in hippocampal slices of newborn and adult rats J Neurochem. 1993 Oct;61(4):1569-72.\u003c\/li\u003e\n\u003cli\u003eCristòfol RM, Rodríguez-Farré E, Sanfeliu C. Effects of glucose and oxygen deprivation on phosphoinositide hydrolysis in cerebral cortex slices from neonatal rats Life Sci. 1996;59(7):587-97.\u003c\/li\u003e\n\u003cli\u003eCui D, Xu J, Xu Q, Zuo G. DL-2-amino-3-phosphonopropionic acid protects primary neurons from oxygen-glucose deprivation induced injury Bosn J Basic Med Sci. 2017 Feb 21;17(1):12-16.\u003c\/li\u003e\n\u003cli\u003eLeonard F, Tschannen W. DL-2-amino-4-(4-pyridyl)butyric acid J Med Chem. 1966 Jan;9(1):140.\u003c\/li\u003e\n\u003cli\u003eFELLOWS EJ, MACKO E, FENDRICK AJ. Pharmacologic data on dl-2-amino-1-(p-methylphenyl)-propane J Pharmacol Exp Ther. 1950 Sep;100(1):72-7.\u003c\/li\u003e\n \u003c\/ul\u003e\n \u003c\/div\u003e\n \u003c\/div\u003e","brand":"Molecular Depot","offers":[{"title":"Default Title","offer_id":50503234421034,"sku":"BTS-B2016229","price":907.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0896\/1579\/4474\/files\/B2016229.png?v=1755359089"},{"product_id":"5-hydroxyindole-3-acetic-acid-highly-pure","title":"5-Hydroxyindole-3-acetic acid (Highly Pure)","description":"\u003cdiv style=\"max-width: 1400px; margin: 0 auto; padding: 40px 20px; font-family: 'Open Sans', sans-serif; font-weight: 300; background: #fff; color: #333; font-size: 0.95rem; box-sizing: border-box;\"\u003e\n \u003cdiv style=\"display: flex; flex-direction: column; gap: 20px;\"\u003e\n \u003cp\u003e\u003cstrong\u003e5-Hydroxyindole-3-acetic acid (Highly Pure)\u003c\/strong\u003e\u003c\/p\u003e\n \u003cdiv style=\"overflow-x: auto; max-width: 100%; margin-bottom: 20px;\"\u003e\n \u003ctable style=\"width: 500px; border-collapse: collapse;\"\u003e\n \u003ctbody\u003e\n \u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eCatalog number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e B2016239\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eLot number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch Dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eExpiration Date:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eAmount:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 2 g\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eMolecular Weight or Concentration:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 191.19 g\/mol\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eSupplied as:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Powder\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eApplications:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e a molecular tool for various biochemical applications\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eStorage:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e -20°C\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eKeywords:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 5-HIAA\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eGrade:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity \u0026gt;18 MΩ-cm) and are filtered through 0.22 um.\u003c\/td\u003e\n \u003c\/tr\u003e\n \u003c\/tbody\u003e\n \u003c\/table\u003e\n \u003c\/div\u003e\n\n \u003chr\u003e\n \u003ch4\u003eReferences\u003c\/h4\u003e\n \n \u003cul style=\"padding-left: 20px; margin: 0;\"\u003e\n \u003cli\u003eRosser EC, Piper CJM, Matei DE, Blair PA, Rendeiro AF, Orford M, Alber DG, Krausgruber T, Catalan D, Klein N, Manson JJ, Drozdov I, Bock C, Wedderburn LR, Eaton S, Mauri C. Microbiota-Derived Metabolites Suppress Arthritis by Amplifying Aryl-Hydrocarbon Receptor Activation in Regulatory B Cells Cell Metab. 2020 Apr 7;31(4):837-851.e10.\u003c\/li\u003e\n\u003cli\u003eJeong YM, Li H, Kim SY, Park WJ, Yun HY, Baek KJ, Kwon NS, Jeong JH, Myung SC, Kim DS. Photo-activated 5-hydroxyindole-3-acetic acid induces apoptosis of prostate and bladder cancer cells J Photochem Photobiol B. 2011 Apr 4;103(1):50-6.\u003c\/li\u003e\n\u003cli\u003eFukui M, Tanaka M, Toda H, Asano M, Yamazaki M, Hasegawa G, Imai S, Nakamura N. High plasma 5-hydroxyindole-3-acetic acid concentrations in subjects with metabolic syndrome Diabetes Care. 2012 Jan;35(1):163-7.\u003c\/li\u003e\n\u003cli\u003eZhang Y, Li L, Gao Y, Wang X, Sun L, Ji W, Ozaki Y. Nitrosonaphthol reaction-assisted SERS assay for selective determination of 5-hydroxyindole-3-acetic acid in human urine Anal Chim Acta. 2020 Oct 16;1134:34-40.\u003c\/li\u003e\n\u003cli\u003eFredj Z, Ali M, Singh B, Dempsey E. Simultaneous voltammetric detection of 5-hydroxyindole-3-acetic acid and 5-hydroxytryptamine using a glassy carbon electrode modified with conducting polymer and platinised carbon nanofibers Mikrochim Acta. 2018 Aug 13;185(9):412.\u003c\/li\u003e\n\u003cli\u003eZhu K, Xu X, Yan B. Ratio Fluorescent Detecting of Tryptophan and Its Metabolite 5-Hydroxyindole-3-acetic Acid Relevant with Depression via Tb(III) Modified HOFs Hybrids: Further Designing Recyclable Molecular Logic Gate Connected by Back Propagation Neural Network Adv Healthc Mater. 2023 Jun;12(15):e2203292.\u003c\/li\u003e\n\u003cli\u003eAfarideh M, Behdadnia A, Noshad S, Mirmiranpour H, Mousavizadeh M, Khajeh E, Rad MV, Mazaheri T, Nakhjavani M, Esteghamati A. ASSOCIATION OF PERIPHERAL 5-HYDROXYINDOLE-3-ACETIC ACID, A SEROTONIN DERIVATIVE, WITH METABOLIC SYNDROME AND LOW-GRADE INFLAMMATION Endocr Pract. 2015 Jul;21(7):711-8.\u003c\/li\u003e\n\u003cli\u003eHu D, Liu J, Yu W, Li C, Huang L, Mao W, Lu Z. Tryptophan intake, not always the more the better Front Nutr. 2023 Apr 11;10:1140054.\u003c\/li\u003e\n\u003cli\u003eHelander A, Wikström T, Löwenmo C, Jacobsson G, Beck O. Urinary excretion of 5-hydroxyindole-3-acetic acid and 5-hydroxytryptophol after oral loading with serotonin Life Sci. 1992;50(17):1207-13.\u003c\/li\u003e\n \u003c\/ul\u003e\n \u003c\/div\u003e\n \u003c\/div\u003e","brand":"Molecular Depot","offers":[{"title":"Default Title","offer_id":50503234453802,"sku":"BTS-B2016239","price":1195.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0896\/1579\/4474\/files\/B2016239.png?v=1755359089"},{"product_id":"5-fluoro-dl-tryptophan-highly-pure","title":"5-Fluoro-DL-tryptophan (Highly Pure)","description":"\u003cdiv style=\"max-width: 1400px; margin: 0 auto; padding: 40px 20px; font-family: 'Open Sans', sans-serif; font-weight: 300; background: #fff; color: #333; font-size: 0.95rem; box-sizing: border-box;\"\u003e\n \u003cdiv style=\"display: flex; flex-direction: column; gap: 20px;\"\u003e\n \u003cp\u003e\u003cstrong\u003e5-Fluoro-DL-tryptophan (Highly Pure)\u003c\/strong\u003e\u003c\/p\u003e\n \u003cdiv style=\"overflow-x: auto; max-width: 100%; margin-bottom: 20px;\"\u003e\n \u003ctable style=\"width: 500px; border-collapse: collapse;\"\u003e\n \u003ctbody\u003e\n \u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eCatalog number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e B2016244\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eLot number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch Dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eExpiration Date:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eAmount:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 50 mg\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eMolecular Weight or Concentration:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 222.22 g\/mol\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eSupplied as:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Powder\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eApplications:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e a molecular tool for various biochemical applications\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eStorage:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 2-8°C\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eKeywords:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e H-5-Fluoro-DL-Trp-OH\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eGrade:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity \u0026gt;18 MΩ-cm) and are filtered through 0.22 um.\u003c\/td\u003e\n \u003c\/tr\u003e\n \u003c\/tbody\u003e\n \u003c\/table\u003e\n \u003c\/div\u003e\n\n \u003chr\u003e\n \u003ch4\u003eReferences\u003c\/h4\u003e\n \n \u003cul style=\"padding-left: 20px; margin: 0;\"\u003e\n \u003cli\u003eAymard N, Honore P, Carbuccia I. Determination of 5-hydroxytryptamine and tryptophan by liquid chromatography in whole blood. Its interest for the exploration of mental disorders Prog Neuropsychopharmacol Biol Psychiatry. 1994 Jan;18(1):77-86.\u003c\/li\u003e\n\u003cli\u003eZhao X, DeVries JS, McDonald R, Sykes BD. Determination of the 19F NMR chemical shielding tensor and crystal structure of 5-fluoro-dl-tryptophan J Magn Reson. 2007 Jul;187(1):88-96.\u003c\/li\u003e\n\u003cli\u003eTraiffort E, Hubert P, Tayeb N, Aymard N. Rapid determination of 5-hydroxytryptamine in whole blood by liquid chromatography with fluorimetric detection J Chromatogr. 1991 Nov 15;571(1-2):231-4.\u003c\/li\u003e\n\u003cli\u003eKinoshita H, Maki Y, Nakai R, Sen K, Shibai H. Competitive amino acid transport between L-tryptophan and other amino acids in Schizophyllum commune J Biosci Bioeng. 2001;92(6):556-9.\u003c\/li\u003e\n\u003cli\u003eFirnau G, Nahmias C, Garnett S. Synthesis of 3,4-dihydroxy-5-fluoro-DL-phenylalanine and 3,4-dihydroxy-5-( 18 F)fluoro-DL-phenylalanine J Med Chem. 1973 Apr;16(4):416-8.\u003c\/li\u003e\n\u003cli\u003eTraiffort E, Hubert P, Tayeb N, Aymard N. Rapid determination of 5-hydroxytryptamine in whole blood by liquid chromatography with fluorimetric detection J Chromatogr. 1991 Nov 15;571(1-2):231-4.\u003c\/li\u003e\n\u003cli\u003eJiang L, Pan T, Lv Q, Yuan W, Liu X, Qu X, Luo D, Wan S, Cui S. Novel ProTide prodrugs of 5-fluoro-2′-deoxyuridine for the treatment of liver cancer Eur J Med Chem. 2023 Nov 15;260:115763.\u003c\/li\u003e\n\u003cli\u003eGe GP, Li CY. (Acetyl-acetonato-κ(2)O,O’)bis-{5-fluoro-2-[3-(4-fluoro-phen-yl)pyrazin-2-yl]phenyl-κ(2)N(1),C(1)}iridium(III) Acta Crystallogr Sect E Struct Rep Online. 2012 Aug 1;68(Pt 8):m1079.\u003c\/li\u003e\n\u003cli\u003eFeng S, Zhu GL, Sun JJ, Chen C, Zhang ZH. Crystal structure of (RS)-4-(3-carb-oxy-1-ethyl-6,8-di-fluoro-4-oxo-1,4-di-hydro-quinolin-7-yl)-2-methyl-piperazin-1-ium 3-carb-oxy-5-fluoro-benzoate Acta Crystallogr E Crystallogr Commun. 2019 Jan 1;75(Pt 1):68-70.\u003c\/li\u003e\n \u003c\/ul\u003e\n \u003c\/div\u003e\n \u003c\/div\u003e","brand":"Molecular Depot","offers":[{"title":"Default Title","offer_id":50503234519338,"sku":"BTS-B2016244","price":595.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0896\/1579\/4474\/files\/B2016244.png?v=1755359092"},{"product_id":"35-diaminobenzoic-acid","title":"3,5-Diaminobenzoic Acid","description":"\u003cdiv style=\"max-width: 1400px; margin: 0 auto; padding: 40px 20px; font-family: 'Open Sans', sans-serif; font-weight: 300; background: #fff; color: #333; font-size: 0.95rem; box-sizing: border-box;\"\u003e\n \u003cdiv style=\"display: flex; flex-direction: column; gap: 20px;\"\u003e\n \u003cp\u003e\u003cstrong\u003e3,5-Diaminobenzoic Acid\u003c\/strong\u003e\u003c\/p\u003e\n \u003cdiv style=\"overflow-x: auto; max-width: 100%; margin-bottom: 20px;\"\u003e\n \u003ctable style=\"width: 500px; border-collapse: collapse;\"\u003e\n \u003ctbody\u003e\n \u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eCatalog number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e B2016172\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eLot number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch Dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eExpiration Date:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eAmount:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 10 g\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eMolecular Weight or Concentration:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 152.15\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eSupplied as:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Powder\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eApplications:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e a molecular tool for various biochemical applications\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eStorage:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e RT, Dry\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eKeywords:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 3,5-Diaminobenzoic Acid\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eGrade:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity \u0026gt;18 MΩ-cm) and are filtered through 0.22 um.\u003c\/td\u003e\n \u003c\/tr\u003e\n \u003c\/tbody\u003e\n \u003c\/table\u003e\n \u003c\/div\u003e\n\n \u003chr\u003e\n \u003ch4\u003eReferences\u003c\/h4\u003e\n \n \u003cul style=\"padding-left: 20px; margin: 0;\"\u003e\n \u003cli\u003eDu C, Ma C, Gu J, Li L, Chen G. Fluorescence Sensing of Caffeine in Tea Beverages with 3,5-diaminobenzoic_Acid Sensors (Basel). 2020 Feb 3;20(3):819.\u003c\/li\u003e\n\u003cli\u003eAnyama CA, Inah B, Utsu P, Ayi AA. Tailoring the band-gap, optical and fluorescent properties of 3,5-diaminobenzoic acid via functionalization with chemical groups: A DFT study Talanta. 2023 Dec 1;265:124777.\u003c\/li\u003e\n\u003cli\u003eChattopadhayay S, Ghosh A, Kumar Mukhopadhyay T, Sharma R, Datta A, Talukdar P. Supramolecular Barrel-Rosette Ion Channel Based on 3,5-Diaminobenzoic Acid for Cation-Anion Symport Angew Chem Int Ed Engl. 2023 Nov 13;62(46):e202313712.\u003c\/li\u003e\n\u003cli\u003eFarag AA, Gafar Afif A, Salih SA, Altalhi AA, Mohamed EA, Mohamed GG. Highly Efficient Elimination of Pb(+2) and Al(+3) Metal Ions from Wastewater Using Graphene Oxide\/3,5-Diaminobenzoic Acid Composites: Selective Removal of Pb(2+) from Real Industrial Wastewater ACS Omega. 2022 Oct 20;7(43):38347-38360.\u003c\/li\u003e\n\u003cli\u003eMulhearn WD, Stafford CM. Highly Permeable Reverse Osmosis Membranes via Molecular Layer-by-Layer Deposition of Trimesoyl Chloride and 3,5-Diaminobenzoic_Acid ACS Appl Polym Mater. 2021;3(1):10.1021\/acsapm.0c01199.\u003c\/li\u003e\n\u003cli\u003ePovedailo VA, Lysenko IL, Tikhomirov SA, Yakovlev DL, Tsybulsky DA, Kruhlik AS, Fan F, Martynenko-Makaev YV, Sharko OL, Duong PV, Minh PH, Shmanai VV. Fluorescent Properties of Carboxyfluorescein Bifluorophores J Fluoresc. 2020 May;30(3):629-635.\u003c\/li\u003e\n\u003cli\u003eBrylev VA, Lysenko IL, Kokin EA, Martynenko-Makaev YV, Ryazantsev DY, Shmanai VV, Korshun VA. Molecular Beacon DNA Probes with Fluorescein Bifluorophore Russ J Bioorg Chem. 2021;47(3):734-740.\u003c\/li\u003e\n\u003cli\u003eGao Y, Dong C, Zhang F, Ma H, Li Y. Constructing Polyimide Aerogels with Carboxyl for CO(2) Adsorption Polymers (Basel). 2022 Jan 18;14(3):359.\u003c\/li\u003e\n\u003cli\u003eSchy WE, Plewa MJ. Use of the diaminobenzoic acid fluorescence assay in conjunction with uv absorbance as a means of quantifying and ascertaining the purity of a DNA preparation Anal Biochem. 1989 Aug 1;180(2):314-8.\u003c\/li\u003e\n \u003c\/ul\u003e\n \u003c\/div\u003e\n \u003c\/div\u003e","brand":"Molecular Depot","offers":[{"title":"Default Title","offer_id":50503234552106,"sku":"BTS-B2016172","price":907.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0896\/1579\/4474\/files\/B2016172.png?v=1755359095"},{"product_id":"n-phosphonomethylglycine","title":"N-(Phosphonomethyl)glycine","description":"\u003cdiv style=\"max-width: 1400px; margin: 0 auto; padding: 40px 20px; font-family: 'Open Sans', sans-serif; font-weight: 300; background: #fff; color: #333; font-size: 0.95rem; box-sizing: border-box;\"\u003e\n \u003cdiv style=\"display: flex; flex-direction: column; gap: 20px;\"\u003e\n \u003cp\u003e\u003cstrong\u003eN-(Phosphonomethyl)glycine\u003c\/strong\u003e\u003c\/p\u003e\n \u003cdiv style=\"overflow-x: auto; max-width: 100%; margin-bottom: 20px;\"\u003e\n \u003ctable style=\"width: 500px; border-collapse: collapse;\"\u003e\n \u003ctbody\u003e\n \u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eCatalog number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e B2016174\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eLot number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch Dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eExpiration Date:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eAmount:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 50 mg\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eMolecular Weight or Concentration:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 169.07\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eSupplied as:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Powder\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eApplications:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e a molecular tool for various biochemical applications\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eStorage:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e RT, Dry\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eKeywords:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Glyphosate\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eGrade:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity \u0026gt;18 MΩ-cm) and are filtered through 0.22 um.\u003c\/td\u003e\n \u003c\/tr\u003e\n \u003c\/tbody\u003e\n \u003c\/table\u003e\n \u003c\/div\u003e\n\n \u003chr\u003e\n \u003ch4\u003eReferences\u003c\/h4\u003e\n \n \u003cul style=\"padding-left: 20px; margin: 0;\"\u003e\n \u003cli\u003eVan Bruggen AHC, He MM, Shin K, Mai V, Jeong KC, Finckh MR, Morris JG Jr. Environmental and health effects of the herbicide glyphosate Sci Total Environ. 2018 Mar;616-617:255-268.\u003c\/li\u003e\n\u003cli\u003eReinbothe S, Nelles A, Parthier B. N-(phosphonomethyl)glycine (glyphosate) tolerance in Euglena gracilis acquired by either overproduced or resistant 5-enolpyruvylshikimate-3-phosphate synthase Eur J Biochem. 1991 Jun 1;198(2):365-73.\u003c\/li\u003e\n\u003cli\u003eMeftaul IM, Venkateswarlu K, Dharmarajan R, Annamalai P, Asaduzzaman M, Parven A, Megharaj M. Controversies over human health and ecological impacts of glyphosate: Is it to be banned in modern agriculture? Environ Pollut. 2020 Aug;263(Pt A):114372.\u003c\/li\u003e\n\u003cli\u003eNaydenova ED, Todorov PT, Topashka-Ancheva MN, Momekov GTs, Yordanova TZ, Konstantinov SM, Troev KD. Novel N-(phosphonomethyl) glycine derivatives: Design, characterization and biological activity Eur J Med Chem. 2008 Jun;43(6):1199-205.\u003c\/li\u003e\n\u003cli\u003eKubena LF, Smalley HE, Farr FM. Influence of glyphosate (N-(phosphonomethyl)glycine) on performance and selected parameters in broilers Poult Sci. 1981 Jan;60(1):132-6.\u003c\/li\u003e\n\u003cli\u003eEkstrom G, Johansson S. Determination of glyphosate (N-phosphonomethyl glycine) using an amino acid analyzer Bull Environ Contam Toxicol. 1975 Sep;14(3):295-300.\u003c\/li\u003e\n\u003cli\u003eMendes A. Research Roundup Br J Community Nurs. 2024 Mar 2;29(3):106-107.\u003c\/li\u003e\n\u003cli\u003eBielecki K, Sarapuk J, Kleszczyńsk H. Binary mixtures of (N-phosphonomethyl)-glycine with new aminophosphonates Z Naturforsch C J Biosci. 2004 Jul-Aug;59(7-8):515-8.\u003c\/li\u003e\n\u003cli\u003eKogevinas M. Probable carcinogenicity of glyphosate BMJ. 2019 Apr 8;365:l1613.\u003c\/li\u003e\n \u003c\/ul\u003e\n \u003c\/div\u003e\n \u003c\/div\u003e","brand":"Molecular Depot","offers":[{"title":"Default Title","offer_id":50503234584874,"sku":"BTS-B2016174","price":595.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0896\/1579\/4474\/files\/B2016174.png?v=1755359095"},{"product_id":"l-alanine-methyl-ester-hydrochloride","title":"L-Alanine Methyl Ester Hydrochloride","description":"\u003cdiv style=\"max-width: 1400px; margin: 0 auto; padding: 40px 20px; font-family: 'Open Sans', sans-serif; font-weight: 300; background: #fff; color: #333; font-size: 0.95rem; box-sizing: border-box;\"\u003e\n \u003cdiv style=\"display: flex; flex-direction: column; gap: 20px;\"\u003e\n \u003cp\u003e\u003cstrong\u003eL-Alanine Methyl Ester Hydrochloride\u003c\/strong\u003e\u003c\/p\u003e\n \u003cdiv style=\"overflow-x: auto; max-width: 100%; margin-bottom: 20px;\"\u003e\n \u003ctable style=\"width: 500px; border-collapse: collapse;\"\u003e\n \u003ctbody\u003e\n \u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eCatalog number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e B2016181\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eLot number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch Dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eExpiration Date:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eAmount:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 1 g\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eMolecular Weight or Concentration:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 139.58\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eSupplied as:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Powder\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eApplications:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e a molecular tool for various biochemical applications\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eStorage:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e RT, Dry\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eKeywords:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e (S)-2-Aminopropionic acid methyl ester hydrochloride, L-Ala-OMe·HCl\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eGrade:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity \u0026gt;18 MΩ-cm) and are filtered through 0.22 um.\u003c\/td\u003e\n \u003c\/tr\u003e\n \u003c\/tbody\u003e\n \u003c\/table\u003e\n \u003c\/div\u003e\n\n \u003chr\u003e\n \u003ch4\u003eReferences\u003c\/h4\u003e\n \n \u003cul style=\"padding-left: 20px; margin: 0;\"\u003e\n \u003cli\u003eLutz M, Schouten A. l-Alanine methyl ester hydro-chloride monohydrate Acta Crystallogr Sect E Struct Rep Online. 2011 Feb 9;67(Pt 3):o586.\u003c\/li\u003e\n\u003cli\u003eHirao Y, Mihara Y, Kira I, Abe I, Yokozeki K. Enzymatic production of L-alanyl-L-glutamine by recombinant E. coli expressing α-amino acid ester acyltransferase from Sphingobacterium siyangensis Biosci Biotechnol Biochem. 2013;77(3):618-23.\u003c\/li\u003e\n\u003cli\u003eAl-Omar MA, Amr Ael-G. Synthesis of some new pyridine-2,6-carboxamide-derived Schiff bases as potential antimicrobial agents Molecules. 2010 Jul 6;15(7):4711-21.\u003c\/li\u003e\n\u003cli\u003eHamed A, Frese M, Elgaafary M, Syrovets T, Sewald N, Simmet T, Shaaban M. Synthesis of novel feruloyl dipeptides with proapoptotic potential against different cancer cell lines Bioorg Chem. 2020 Apr;97:103678.\u003c\/li\u003e\n\u003cli\u003ePinilla L, Gonzalez LC, Tena-Sempere M, Aguilar E. 5-HT1 and 5-HT2 receptor activation reduces N-methyl-D-aspartate (NMDA)-stimulated LH secretion in prepubertal male and female rats Eur J Endocrinol. 2003 Jan;148(1):121-7.\u003c\/li\u003e\n\u003cli\u003eCheng C, Cai Z, Peng XS, Wong HN. Enantiomeric recognition of amino acid salts by macrocyclic crown ethers derived from enantiomerically pure 1,8,9,16-tetrahydroxytetraphenylenes J Org Chem. 2013 Sep 6;78(17):8562-73.\u003c\/li\u003e\n\u003cli\u003eBornaghi LF, Poulsen SA, Healy PC, White AR. N-Cinnamoyl-l-phenyl-alanine methyl ester Acta Crystallogr Sect E Struct Rep Online. 2007 Dec 6;64(Pt 1):o139.\u003c\/li\u003e\n\u003cli\u003eLi BS, Lam JW, Yu ZQ, Tang BZ. Tunable helical assemblies of L-alanine methyl ester-containing polyphenylacetylene Langmuir. 2012 Apr 3;28(13):5770-4.\u003c\/li\u003e\n\u003cli\u003eKaurav H, Kapoor DN. Implantable systems for drug delivery to the brain Ther Deliv. 2017 Dec;8(12):1097-1107.\u003c\/li\u003e\n \u003c\/ul\u003e\n \u003c\/div\u003e\n \u003c\/div\u003e","brand":"Molecular Depot","offers":[{"title":"Default Title","offer_id":50503234650410,"sku":"BTS-B2016181","price":595.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0896\/1579\/4474\/files\/B2016181.png?v=1755359098"},{"product_id":"d-alanine-7-amido-4-methylcoumarin","title":"D-Alanine-7-Amido-4-Methylcoumarin","description":"\u003cdiv style=\"max-width: 1400px; margin: 0 auto; padding: 40px 20px; font-family: 'Open Sans', sans-serif; font-weight: 300; background: #fff; color: #333; font-size: 0.95rem; box-sizing: border-box;\"\u003e\n \u003cdiv style=\"display: flex; flex-direction: column; gap: 20px;\"\u003e\n \u003cp\u003e\u003cstrong\u003eD-Alanine-7-Amido-4-Methylcoumarin\u003c\/strong\u003e\u003c\/p\u003e\n \u003cdiv style=\"overflow-x: auto; max-width: 100%; margin-bottom: 20px;\"\u003e\n \u003ctable style=\"width: 500px; border-collapse: collapse;\"\u003e\n \u003ctbody\u003e\n \u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eCatalog number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e B2016193\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eLot number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch Dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eExpiration Date:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eAmount:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 5 mg\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eMolecular Weight or Concentration:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 360.3\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eSupplied as:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Powder\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eApplications:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e a molecular tool for various biochemical applications\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eStorage:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e -20°C\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eKeywords:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e D-Alanine-7-Amido-4-Methylcoumarin Trifluoroacetate\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eGrade:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity \u0026gt;18 MΩ-cm) and are filtered through 0.22 um.\u003c\/td\u003e\n \u003c\/tr\u003e\n \u003c\/tbody\u003e\n \u003c\/table\u003e\n \u003c\/div\u003e\n\n \u003chr\u003e\n \u003ch4\u003eReferences\u003c\/h4\u003e\n \n \u003cul style=\"padding-left: 20px; margin: 0;\"\u003e\n \u003cli\u003eSobczak AJ, Chbib C, Wnuk SF. S-Ribosylhomocysteine analogs containing a [4-thio]ribose ring Carbohydr Res. 2015 Oct 13;415:39-47.\u003c\/li\u003e\n\u003cli\u003eTsukanov SV, Comins DL. Total synthesis of alkaloid 205B J Org Chem. 2014 Oct 3;79(19):9074-85.\u003c\/li\u003e\n\u003cli\u003eVinaya, Basavaraju YB, Yathirajan HS, Parkin S. Syntheses and crystal structures of four 4-(4-meth-oxy-phen-yl)piperazin-1-ium salts: tri-fluoro-acetate, 2,3,4,5,6-penta-fluoro-benzoate, 4-iodo-benzoate, and a polymorph with 4-methyl-benzoate Acta Crystallogr E Crystallogr Commun. 2023 Mar 23;79(Pt 4):380-385.\u003c\/li\u003e\n\u003cli\u003eHirsch J, Petrakova E, Feather MS, Barnes CL. The reaction of D-glucose with aminoguanidine Carbohydr Res. 1995 Feb 1;267(1):17-25.\u003c\/li\u003e\n\u003cli\u003eAoyama J, Osaka M, Deushi M, Hosoya S, Ishigami A, Maehara T, Yoshida M. CXCL1-Triggered PAD4 Cytoplasmic Translocation Enhances Neutrophil Adhesion through Citrullination of PDIA1 J Atheroscler Thromb. 2022 Sep 1;29(9):1307-1318.\u003c\/li\u003e\n\u003cli\u003eSun ZH, Sun WM, Chen CT, Zhang GH, Wang XQ, Xu D. L-arginine trifluoroacetate salt bridges in its solid state compound: the low-temperature three dimensional structural determination of L-arginine bis(trifluoroacetate) crystal and its vibrational spectral analysis Spectrochim Acta A Mol Biomol Spectrosc. 2011 Dec;83(1):39-45.\u003c\/li\u003e\n\u003cli\u003eBalasekaran SM, Hagenbach A, Drees M, Abram U. [Tc(II)(NO)(trifluoroacetate)(4)F](2-) – synthesis and reactions Dalton Trans. 2017 Oct 10;46(39):13544-13552.\u003c\/li\u003e\n\u003cli\u003eCheong WJ, Ali F, Kim YS, Lee JW. Comprehensive overview of recent preparation and application trends of various open tubular capillary columns in separation science J Chromatogr A. 2013 Sep 20;1308:1-24.\u003c\/li\u003e\n\u003cli\u003eBussolati B, Ribatti D, Munaron L, Bartorelli A, Bussolati G. Anti-angiogenic properties of calcium trifluoroacetate Microvasc Res. 2009 Dec;78(3):272-7.\u003c\/li\u003e\n \u003c\/ul\u003e\n \u003c\/div\u003e\n \u003c\/div\u003e","brand":"Molecular Depot","offers":[{"title":"Default Title","offer_id":50503234748714,"sku":"BTS-B2016193","price":907.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0896\/1579\/4474\/files\/B2016193.png?v=1755359105"},{"product_id":"d-biotin-highly-pure","title":"D(+)-Biotin (Highly Pure)","description":"\u003cdiv style=\"max-width: 1400px; margin: 0 auto; padding: 40px 20px; font-family: 'Open Sans', sans-serif; font-weight: 300; background: #fff; color: #333; font-size: 0.95rem; box-sizing: border-box;\"\u003e\n \u003cdiv style=\"display: flex; flex-direction: column; gap: 20px;\"\u003e\n \u003cp\u003e\u003cstrong\u003eD(+)-Biotin (Highly Pure)\u003c\/strong\u003e\u003c\/p\u003e\n \u003cdiv style=\"overflow-x: auto; max-width: 100%; margin-bottom: 20px;\"\u003e\n \u003ctable style=\"width: 500px; border-collapse: collapse;\"\u003e\n \u003ctbody\u003e\n \u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eCatalog number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e B2016195\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eLot number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch Dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eExpiration Date:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eAmount:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 250 mg\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eMolecular Weight or Concentration:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 244.31\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eSupplied as:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Powder\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eApplications:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e a molecular tool for various biochemical applications\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eStorage:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e RT, Dry\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eKeywords:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e D(+)-Biotin, D-Biotin,Vitamin H, Hexahydro-2-oxothieno(3,4-d)-imidazole-4-pentanoic acid, Vitamin H\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eGrade:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity \u0026gt;18 MΩ-cm) and are filtered through 0.22 um.\u003c\/td\u003e\n \u003c\/tr\u003e\n \u003c\/tbody\u003e\n \u003c\/table\u003e\n \u003c\/div\u003e\n\n \u003chr\u003e\n \u003ch4\u003eReferences\u003c\/h4\u003e\n \n \u003cul style=\"padding-left: 20px; margin: 0;\"\u003e\n \u003cli\u003eNagase Y, Matsumoto U, Shimada K. [Polymorphism of d-biotin] Yakugaku Zasshi. 1969 Apr;89(4):595-7.\u003c\/li\u003e\n\u003cli\u003eBIRNBAUM J, LICHSTEIN HC. CONVERSION OF D-BIOTIN TO BIOTIN VITAMERS BY LACTOBACILLUS ARABINOSUS J Bacteriol. 1965 Apr;89(4):1035-40.\u003c\/li\u003e\n\u003cli\u003eDing Z, Wang S, Shi Y, Fei X, Cheng B, Lu Y, Chen J. Discovery of Novel d-(+)-Biotin-Conjugated Resorcinol Dibenzyl Ether-Based PD-L1 Inhibitors for Targeted Cancer Immunotherapy J Med Chem. 2023 Aug 10;66(15):10364-10380.\u003c\/li\u003e\n\u003cli\u003eZhang Y, Wang R, Dong Y, Huang G, Ji B, Wang Q. Assessment of biotin interference in thyroid function tests Medicine (Baltimore). 2020 Feb;99(9):e19232.\u003c\/li\u003e\n\u003cli\u003eDuchi S, Rebollo Torregrosa P, Hajuj A, Molho D, Shkoor R, Saada NA, Fernández DG, Goldstein D, Pérez-Fernández A. The formulation and in vitro evaluation of WS Biotin, a novel encapsulated form of D-Biotin with improved water solubility for hair and skin treatment applications Int J Cosmet Sci. 2024 Feb;46(1):119-129.\u003c\/li\u003e\n\u003cli\u003eMELVILLE DB. Biotin sulfoxide J Biol Chem. 1954 Jun;208(2):495-501.\u003c\/li\u003e\n\u003cli\u003eViswanathan V, Mahn FP, Venturella VS, Senkowski BZ. Gas-liquid chromatography of d-biotin J Pharm Sci. 1970 Mar;59(3):400-2.\u003c\/li\u003e\n\u003cli\u003eSuganuma M, Kubo T, Ishiki K, Tanaka K, Suto K, Ejima D, Toyota M, Tsumoto K, Sato T, Nishikawa Y. Mirror-image streptavidin with specific binding to L-biotin, the unnatural enantiomer Sci Rep. 2022 Jun 10;12(1):9568.\u003c\/li\u003e\n\u003cli\u003eGunsolus IL, Matias M, Prostko J, Mohr P, Sokoll LJ. Prevalence of Detectable Biotin in Five US Emergency Department Patient Cohorts Clin Biochem. 2021 Jul;93:26-32.\u003c\/li\u003e\n \u003c\/ul\u003e\n \u003c\/div\u003e\n \u003c\/div\u003e","brand":"Molecular Depot","offers":[{"title":"Default Title","offer_id":50503234912554,"sku":"BTS-B2016195","price":907.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0896\/1579\/4474\/files\/B2016195.png?v=1755359104"},{"product_id":"n-benzyloxycarbonyloxysuccinimide","title":"N-(Benzyloxycarbonyloxy)succinimide","description":"\u003cdiv style=\"max-width: 1400px; margin: 0 auto; padding: 40px 20px; font-family: 'Open Sans', sans-serif; font-weight: 300; background: #fff; color: #333; font-size: 0.95rem; box-sizing: border-box;\"\u003e\n \u003cdiv style=\"display: flex; flex-direction: column; gap: 20px;\"\u003e\n \u003cp\u003e\u003cstrong\u003eN-(Benzyloxycarbonyloxy)succinimide\u003c\/strong\u003e\u003c\/p\u003e\n \u003cdiv style=\"overflow-x: auto; max-width: 100%; margin-bottom: 20px;\"\u003e\n \u003ctable style=\"width: 500px; border-collapse: collapse;\"\u003e\n \u003ctbody\u003e\n \u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eCatalog number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e B2016196\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eLot number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch Dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eExpiration Date:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eAmount:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 5 g\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eMolecular Weight or Concentration:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 249.22\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eSupplied as:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Powder\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eApplications:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e a molecular tool for various biochemical applications\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eStorage:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e RT, Dry\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eKeywords:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Benzyl N-succinimidyl carbonate, Z-OSu\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eGrade:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity \u0026gt;18 MΩ-cm) and are filtered through 0.22 um.\u003c\/td\u003e\n \u003c\/tr\u003e\n \u003c\/tbody\u003e\n \u003c\/table\u003e\n \u003c\/div\u003e\n\n \u003chr\u003e\n \u003ch4\u003eReferences\u003c\/h4\u003e\n \n \u003cul style=\"padding-left: 20px; margin: 0;\"\u003e\n \u003cli\u003eTavaré R, Torres Martin De Rosales R, Blower PJ, Mullen GE. Efficient site-specific radiolabeling of a modified C2A domain of synaptotagmin I with [99mTc(CO)3]+: a new radiopharmaceutical for imaging cell death Bioconjug Chem. 2009 Nov;20(11):2071-81.\u003c\/li\u003e\n\u003cli\u003eShiozaki M, Arai M, Hiraoka T, Nishijima M, Akamatsu Y. Synthesis of 2-deoxy-2-[(2R,3S)-2-fluoro-3-hydroxytetradecanamido]- 3-O-[(3R)-3-hydroxytetradecanoyl]-4-O-phosphono-D-glucopyranose and its (2S,3R)-isomer Biosci Biotechnol Biochem. 1993 Sep;57(9):1526-9.\u003c\/li\u003e\n\u003cli\u003eShiozaki M, Kobayashi Y, Arai M, Watanabe T, Hiraoka T. Synthesis of 2-deoxy-2-[(2,2-difluoro-3-hydroxytetradecanoyl)amino]-3-O- [(R)-3-(tetradecanoyloxy)tetradecanoyl]-D-glucopyranose 4-phosphate J Med Chem. 1991 Aug;34(8):2643-6.\u003c\/li\u003e\n\u003cli\u003eZhao Z, Yue J, Ji X, Nian M, Kang K, Qiao H, Zheng X. Research progress in biological activities of succinimide derivatives Bioorg Chem. 2021 Mar;108:104557.\u003c\/li\u003e\n\u003cli\u003eRenaudet O, Dumy P, Philouze C, Averbuch-Pouchot MT. N-(2-Acetamido-3,4,6-tri-O-acetyl-2-deoxy-alpha-D-galactopyranosyloxy)succinimide Acta Crystallogr C. 2001 May;57(Pt 5):649-50.\u003c\/li\u003e\n\u003cli\u003eParsons WH, Rutland NT, Crainic JA, Cardozo JM, Chow AS, Andrews CL, Sheehan BK. Development of succinimide-based inhibitors for the mitochondrial rhomboid protease PARL Bioorg Med Chem Lett. 2021 Oct 1;49:128290.\u003c\/li\u003e\n\u003cli\u003eLi YF, Wei YF, Tian J, Zhang J, Chang HH, Gao WC. N-Thiohydroxy Succinimide Esters (NTSEs): Versatile Reagents for Selective Acyl and Acylthio Transfer Org Lett. 2022 Aug 12;24(31):5736-5740.\u003c\/li\u003e\n\u003cli\u003eNowak C, Ponniah G, Neill A, Liu H. Characterization of succinimide stability during trypsin digestion for LC-MS analysis Anal Biochem. 2017 Jun 1;526:1-8.\u003c\/li\u003e\n\u003cli\u003eVanAernum ZL, Sergi JA, Dey M, Toner T, Kilgore B, Lay-Fortenbery A, Wang Y, Bian S, Kochert BA, Bothe JR, Gao X, Richardson D, Schuessler HA. Discovery and Control of Succinimide Formation and Accumulation at Aspartic Acid Residues in The Complementarity-Determining Region of a Therapeutic Monoclonal Antibody Pharm Res. 2023 Jun;40(6):1411-1423.\u003c\/li\u003e\n \u003c\/ul\u003e\n \u003c\/div\u003e\n \u003c\/div\u003e","brand":"Molecular Depot","offers":[{"title":"Default Title","offer_id":50503234945322,"sku":"BTS-B2016196","price":907.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0896\/1579\/4474\/files\/B2016196.png?v=1755359108"},{"product_id":"l-asparagine-monohydrate","title":"L-Asparagine monohydrate","description":"\u003cdiv style=\"max-width: 1400px; margin: 0 auto; padding: 40px 20px; font-family: 'Open Sans', sans-serif; font-weight: 300; background: #fff; color: #333; font-size: 0.95rem; box-sizing: border-box;\"\u003e\n \u003cdiv style=\"display: flex; flex-direction: column; gap: 20px;\"\u003e\n \u003cp\u003e\u003cstrong\u003eL-Asparagine monohydrate\u003c\/strong\u003e\u003c\/p\u003e\n \u003cdiv style=\"overflow-x: auto; max-width: 100%; margin-bottom: 20px;\"\u003e\n \u003ctable style=\"width: 500px; border-collapse: collapse;\"\u003e\n \u003ctbody\u003e\n \u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eCatalog number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e B2016203\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eLot number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch Dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eExpiration Date:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eAmount:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 10 g\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eMolecular Weight or Concentration:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 150.13\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eSupplied as:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Powder\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eApplications:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e a molecular tool for various biochemical applications\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eStorage:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e RT, Dry\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eKeywords:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e (S)-(+)-2-Aminosuccinamic acid, (S)-2-Aminosuccinic acid 4-amide, L-Aspartic acid 4-amide\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eGrade:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity \u0026gt;18 MΩ-cm) and are filtered through 0.22 um.\u003c\/td\u003e\n \u003c\/tr\u003e\n \u003c\/tbody\u003e\n \u003c\/table\u003e\n \u003c\/div\u003e\n\n \u003chr\u003e\n \u003ch4\u003eReferences\u003c\/h4\u003e\n \n \u003cul style=\"padding-left: 20px; margin: 0;\"\u003e\n \u003cli\u003eRahman MA, Podder J, Das H. Growth, structural, thermal, and optical characteristics of L-asparagine monohydrate doped magnesium sulphate heptahydrate semiorganic crystals Heliyon. 2023 Nov 14;9(11):e22322.\u003c\/li\u003e\n\u003cli\u003eGomes EJ, Lima JA Jr, Freire PTC, Pinheiro GS, de Sousa FF, Remédios CMR. Effect of Fe (III) on L-asparagine monohydrate investigated under low- and high-temperature conditions Spectrochim Acta A Mol Biomol Spectrosc. 2020 Nov 5;241:118643.\u003c\/li\u003e\n\u003cli\u003ede Oliveira RC, Ferreira Júnior MNG, Calligaris GA, Dos Santos AO, Remédios CMR. Synchrotron radiation X-ray diffraction and Raman spectroscopy study of l-asparagine monohydrate doped with Fe(III) at high pressure Spectrochim Acta A Mol Biomol Spectrosc. 2022 Dec 15;283:121716.\u003c\/li\u003e\n\u003cli\u003eSchilling K, Amstalden MC, Meinel L, Holzgrabe U. Impurity profiling of l-asparagine monohydrate by ion pair chromatography applying low wavelength UV detection J Pharm Biomed Anal. 2016 Nov 30;131:202-207.\u003c\/li\u003e\n\u003cli\u003ede Moraes LS, Kennedy AR, Logan CR. Crystal structures of three halide salts of l-asparagine: an isostructural series Acta Crystallogr E Crystallogr Commun. 2018 Oct 19;74(Pt 11):1619-1623.\u003c\/li\u003e\n\u003cli\u003eShkir M, Muhammad S, AlFaify S, Irfan A, Yahia IS. A dual approach to study the electro-optical properties of a noncentrosymmetric L-asparagine monohydrate Spectrochim Acta A Mol Biomol Spectrosc. 2015 Feb 25;137:432-41.\u003c\/li\u003e\n\u003cli\u003eSylvestre S, Sebastian S, Edwin S, Amalanathan M, Ayyapan S, Jayavarthanan T, Oudayakumar K, Solomon S. Vibrational spectra (FT-IR and FT-Raman), molecular structure, natural bond orbital, and TD-DFT analysis of L-Asparagine Monohydrate by Density Functional Theory approach Spectrochim Acta A Mol Biomol Spectrosc. 2014 Dec 10;133:190-200.\u003c\/li\u003e\n\u003cli\u003eGörbitz CH, Hartviksen LM. The monohydrates of the four polar dipeptides L-seryl-L-asparagine, L-seryl-L-tyrosine, L-tryptophanyl-L-serine and L-tyrosyl-L-tryptophan Acta Crystallogr C. 2008 Mar;64(Pt 3):o171-6.\u003c\/li\u003e\n\u003cli\u003eDelbaere LT. The molecular and crystal structures of 4-N-(2-acetamido-2-deoxy-beta-D-glucopyranosyl)-L-asparagine trihydrate and 4-N-(beta-D-glucopyranosyl)-L-asparagine monohydrate. The x-ray analysis of a carbohydrate-peptide linkage Biochem J. 1974 Oct;143(1):197-205.\u003c\/li\u003e\n \u003c\/ul\u003e\n \u003c\/div\u003e\n \u003c\/div\u003e","brand":"Molecular Depot","offers":[{"title":"Default Title","offer_id":50503235010858,"sku":"BTS-B2016203","price":907.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0896\/1579\/4474\/files\/B2016203.png?v=1755359109"},{"product_id":"l-proline-methyl-ester-hydrochloride","title":"L-Proline Methyl Ester Hydrochloride","description":"\u003cdiv style=\"max-width: 1400px; margin: 0 auto; padding: 40px 20px; font-family: 'Open Sans', sans-serif; font-weight: 300; background: #fff; color: #333; font-size: 0.95rem; box-sizing: border-box;\"\u003e\n \u003cdiv style=\"display: flex; flex-direction: column; gap: 20px;\"\u003e\n \u003cp\u003e\u003cstrong\u003eL-Proline Methyl Ester Hydrochloride\u003c\/strong\u003e\u003c\/p\u003e\n \u003cdiv style=\"overflow-x: auto; max-width: 100%; margin-bottom: 20px;\"\u003e\n \u003ctable style=\"width: 500px; border-collapse: collapse;\"\u003e\n \u003ctbody\u003e\n \u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eCatalog number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e B2016123\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eLot number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch Dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eExpiration Date:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eAmount:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 250 mg\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eMolecular Weight or Concentration:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 165.62\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eSupplied as:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Powder\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eApplications:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e a molecular tool for various biochemical applications\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eStorage:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e RT, Dry\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eKeywords:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e (S)-Methyl pyrrolidine-2-carboxylate hydrochloride, L-Pro-OMe HCl\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eGrade:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity \u0026gt;18 MΩ-cm) and are filtered through 0.22 um.\u003c\/td\u003e\n \u003c\/tr\u003e\n \u003c\/tbody\u003e\n \u003c\/table\u003e\n \u003c\/div\u003e\n\n \u003chr\u003e\n \u003ch4\u003eReferences\u003c\/h4\u003e\n \n \u003cul style=\"padding-left: 20px; margin: 0;\"\u003e\n \u003cli\u003eZheng L, Zhao Z, Yang Y, Li Y, Wang C. Novel skin permeation enhancers based on amino acid ester ionic liquid: Design and permeation mechanism Int J Pharm. 2020 Feb 25;576:119031.\u003c\/li\u003e\n\u003cli\u003eSeth MK, Hussain ME, Pasha S, Fahim M. Effects of a novel ACE inhibitor, 3-(3-thienyl)-l-alanyl-ornithyl-proline, on endothelial vasodilation and hepatotoxicity in l-NAME-induced hypertensive rats Drug Des Devel Ther. 2016 Apr 20;10:1533-42.\u003c\/li\u003e\n\u003cli\u003eSekii Y, Kiuchi H, Takezawa K, Imanaka T, Kuribayashi S, Okada K, Inagaki Y, Ueda N, Fukuhara S, Imamura R, Negoro H, Nonomura N. Dietary salt with nitric oxide deficiency induces nocturnal polyuria in mice via hyperactivation of intrarenal angiotensin II-SPAK-NCC pathway Commun Biol. 2022 Feb 28;5(1):175.\u003c\/li\u003e\n\u003cli\u003eMishra V, Singh VP. Implication of nitric oxide and hydrogen sulfide signalling in alleviating arsenate stress in rice seedlings Environ Pollut. 2021 Dec 15;291:117958.\u003c\/li\u003e\n\u003cli\u003eKaya C, Polat T, Ashraf M, Kaushik P, Alyemeni MN, Ahmad P. Endogenous nitric oxide and its potential sources regulate glutathione-induced cadmium stress tolerance in maize plants Plant Physiol Biochem. 2021 Oct;167:723-737.\u003c\/li\u003e\n\u003cli\u003eNonaka A, Nakamura T, Hirota T, Matsushita A, Asakura M, Ohki K, Kitakaze M. The milk-derived peptides Val-Pro-Pro and Ile-Pro-Pro attenuate arterial dysfunction in L-NAME-treated rats Hypertens Res. 2014 Aug;37(8):703-7.\u003c\/li\u003e\n\u003cli\u003eZhang ZY, Feng XY, Wang ZH, Huang YZ, Yang WB, Zhang WJ, Zhou J, Yuan ZY. [Similarities and differences of myocardial metabolic characteristics between HFpEF and HFrEF mice based on LC-MS\/MS metabolomics] Zhonghua Xin Xue Guan Bing Za Zhi. 2023 Jul 24;51(7):722-730.\u003c\/li\u003e\n\u003cli\u003eBunbupha S, Pakdeechote P, Maneesai P, Prachaney P, Boonprom P. Carthamus Tinctorius L. extract attenuates cardiac remodeling in L-NAME-induced hypertensive rats by inhibiting the NADPH oxidase-mediated TGF-β1 and MMP-9 pathway Ann Anat. 2019 Mar;222:120-128.\u003c\/li\u003e\n\u003cli\u003eYamane M, Moriya S, Kokuba H. Visualization of ceramide channels in lysosomes following endogenous palmitoyl-ceramide accumulation as an initial step in the induction of necrosis Biochem Biophys Rep. 2017 Mar 13;11:174-181.\u003c\/li\u003e\n \u003c\/ul\u003e\n \u003c\/div\u003e\n \u003c\/div\u003e","brand":"Molecular Depot","offers":[{"title":"Default Title","offer_id":50503235731754,"sku":"BTS-B2016123","price":595.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0896\/1579\/4474\/files\/B2016123.png?v=1755359130"},{"product_id":"n-tosyl-l-alanine-3-indoxyl-ester","title":"N-Tosyl-L-alanine 3-indoxyl Ester","description":"\u003cdiv style=\"max-width: 1400px; margin: 0 auto; padding: 40px 20px; font-family: 'Open Sans', sans-serif; font-weight: 300; background: #fff; color: #333; font-size: 0.95rem; box-sizing: border-box;\"\u003e\n \u003cdiv style=\"display: flex; flex-direction: column; gap: 20px;\"\u003e\n \u003cp\u003e\u003cstrong\u003eN-Tosyl-L-alanine 3-indoxyl Ester\u003c\/strong\u003e\u003c\/p\u003e\n \u003cdiv style=\"overflow-x: auto; max-width: 100%; margin-bottom: 20px;\"\u003e\n \u003ctable style=\"width: 500px; border-collapse: collapse;\"\u003e\n \u003ctbody\u003e\n \u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eCatalog number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e B2016125\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eLot number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch Dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eExpiration Date:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eAmount:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 25 mg\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eMolecular Weight or Concentration:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 358.42 g\/mol\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eSupplied as:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Powder\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eApplications:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e a molecular tool for various biochemical applications\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eStorage:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e -20°C\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eKeywords:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Tos-Ala-Y\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eGrade:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity \u0026gt;18 MΩ-cm) and are filtered through 0.22 um.\u003c\/td\u003e\n \u003c\/tr\u003e\n \u003c\/tbody\u003e\n \u003c\/table\u003e\n \u003c\/div\u003e\n\n \u003chr\u003e\n \u003ch4\u003eReferences\u003c\/h4\u003e\n \n \u003cul style=\"padding-left: 20px; margin: 0;\"\u003e\n \u003cli\u003eMendes JA, Salustiano EJ, Pires CS, Oliveira T, Barcellos JCF, Cifuentes JMC, Costa PRR, Rennó MN, Buarque CD. 11a-N-tosyl-5-carbapterocarpans: Synthesis, antineoplastic evaluation and in silico prediction of ADMETox properties Bioorg Chem. 2018 Oct;80:585-590.\u003c\/li\u003e\n\u003cli\u003eShen HS, Liu N, Li ZC, Huang WC. N-Ethyl-N-phenyl-N’-tosyl-formamidine Acta Crystallogr Sect E Struct Rep Online. 2009 Jun 17;65(Pt 7):o1582.\u003c\/li\u003e\n\u003cli\u003eMeng XZ, Wan XJ. (E)-2-Phenyl-N-tosyl-non-2-en-4-ynamide Acta Crystallogr Sect E Struct Rep Online. 2013 Jan 1;69(Pt 1):o78.\u003c\/li\u003e\n\u003cli\u003eYoshioka S, Takatsuki M, Takehara T, Suzuki T, Arisawa M. Development of Cycloisomerization with Rearrangement of a Tosyl Group Using N-Tosyl-o-allenylaniline J Org Chem. 2023 Aug 4;88(15):11268-11277.\u003c\/li\u003e\n\u003cli\u003eLo A, Gutierrez DA, Toth-Williams G, Fettinger JC, Shaw JT. 1,3-Asymmetric Induction in Diastereoselective Allylations of Chiral N-Tosyl Imines J Org Chem. 2022 Mar 4;87(5):2773-2778.\u003c\/li\u003e\n\u003cli\u003eHuang ML. Aqua-{N-[(4-methyl-phen-yl)sulfon-yl]glycinato(2-)-κN,O}(1,10-phenan-throline)copper(II) Acta Crystallogr Sect E Struct Rep Online. 2010 Sep 15;66(Pt 10):m1255.\u003c\/li\u003e\n\u003cli\u003eWu M, Hu YM. 2-Tosyl-2,3,3a,4,9,9a-hexa-hydro-1H-benzo[f]isoindol-1-one Acta Crystallogr Sect E Struct Rep Online. 2013 May 18;69(Pt 6):o926.\u003c\/li\u003e\n\u003cli\u003eN Al-Mohammed N, Alias Y, Abdullah Z, Khaledi H. 1-Tosyl-2-[(1-tosyl-1H-benzimidazol-2-yl)methyl-sulfanyl]-1H-benzimidazole Acta Crystallogr Sect E Struct Rep Online. 2011 May 1;67(Pt 5):o1043.\u003c\/li\u003e\n\u003cli\u003eBennett JM, Shapiro JD, Choinski KN, Mei Y, Aulita SM, Dominguez GM, Majireck MM. Preparation of N-(2-alkoxyvinyl)sulfonamides from N-tosyl-1,2,3-triazoles and Subsequent Conversion to Substituted Phthalans and Phenethylamines J Vis Exp. 2018 Jan 3;(131):56848.\u003c\/li\u003e\n \u003c\/ul\u003e\n \u003c\/div\u003e\n \u003c\/div\u003e","brand":"Molecular Depot","offers":[{"title":"Default Title","offer_id":50503236288810,"sku":"BTS-B2016125","price":907.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0896\/1579\/4474\/files\/B2016125.png?v=1755359142"},{"product_id":"n-acetyl-l-carnosine-highly-pure","title":"N-Acetyl-L-carnosine (Highly Pure)","description":"\u003cdiv style=\"max-width: 1400px; margin: 0 auto; padding: 40px 20px; font-family: 'Open Sans', sans-serif; font-weight: 300; background: #fff; color: #333; font-size: 0.95rem; box-sizing: border-box;\"\u003e\n \u003cdiv style=\"display: flex; flex-direction: column; gap: 20px;\"\u003e\n \u003cp\u003e\u003cstrong\u003eN-Acetyl-L-carnosine (Highly Pure)\u003c\/strong\u003e\u003c\/p\u003e\n \u003cdiv style=\"overflow-x: auto; max-width: 100%; margin-bottom: 20px;\"\u003e\n \u003ctable style=\"width: 500px; border-collapse: collapse;\"\u003e\n \u003ctbody\u003e\n \u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eCatalog number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e B2016126\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eLot number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch Dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eExpiration Date:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eAmount:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 1 g\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eMolecular Weight or Concentration:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 268.27 g\/mol\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eSupplied as:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Powder\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eApplications:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e a molecular tool for various biochemical applications\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eStorage:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e RT\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eKeywords:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e N-Acetylcarnosine\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eGrade:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity \u0026gt;18 MΩ-cm) and are filtered through 0.22 um.\u003c\/td\u003e\n \u003c\/tr\u003e\n \u003c\/tbody\u003e\n \u003c\/table\u003e\n \u003c\/div\u003e\n\n \u003chr\u003e\n \u003ch4\u003eReferences\u003c\/h4\u003e\n \n \u003cul style=\"padding-left: 20px; margin: 0;\"\u003e\n \u003cli\u003eAbdelkader H, Longman MR, Alany RG, Pierscionek B. Phytosome-hyaluronic acid systems for ocular delivery of L-carnosine Int J Nanomedicine. 2016 Jun 14;11:2815-27.\u003c\/li\u003e\n\u003cli\u003eLiu M, Lu J, Chen Y, Shi X, Li Y, Yang S, Yu J, Guan S. Sodium Sulfite-Induced Mast Cell Pyroptosis and Degranulation J Agric Food Chem. 2021 Jul 14;69(27):7755-7764.\u003c\/li\u003e\n\u003cli\u003eOkabe S, Kunimi H. Effects of N-acetyl-L-carnosine aluminum (CL-1700) on various acute gastric lesions and gastric secretion in rats Jpn J Pharmacol. 1981 Dec;31(6):941-50.\u003c\/li\u003e\n\u003cli\u003eBadawi A, Mohammed M, Khalil R, Ali R, Taleb SA. Effectuation of loading a natural acetyl carnosine derivative within a promising cross-linked cyclodextrin spongey-like nanospheres on Physicochemical characterization and release behavior Pak J Pharm Sci. 2021 Jan;34(1(Supplementary)):283-290.\u003c\/li\u003e\n\u003cli\u003eGoebel AS, Schmaus G, Neubert RH, Wohlrab J. Dermal peptide delivery using enhancer molecules and colloidal carrier systems–part I: carnosine Skin Pharmacol Physiol. 2012;25(6):281-7.\u003c\/li\u003e\n\u003cli\u003eKunimi H, Okabe S. Effects of CL-1700 and its constituents on acute or chronic gastric lesions and gastric secretion in rats Jpn J Pharmacol. 1982 Jun;32(3):469-77.\u003c\/li\u003e\n\u003cli\u003eDobson AJ, Gerkin RE. N-acetyl-L-glutamic acid Acta Crystallogr C. 1997 Jan 15;53 ( Pt 1):73-6.\u003c\/li\u003e\n\u003cli\u003eXing S, Guo Z, Lang J, Zhou M, Cao J, He H, Yu L, Zhou Y. N-Acetyl-l-cysteine ameliorates gestational diabetes mellitus by inhibiting oxidative stress Gynecol Endocrinol. 2023 Dec;39(1):2189969.\u003c\/li\u003e\n\u003cli\u003eCalzetta L, Matera MG, Rogliani P, Cazzola M. Multifaceted activity of N-acetyl-l-cysteine in chronic obstructive pulmonary disease Expert Rev Respir Med. 2018 Aug;12(8):693-708.\u003c\/li\u003e\n \u003c\/ul\u003e\n \u003c\/div\u003e\n \u003c\/div\u003e","brand":"Molecular Depot","offers":[{"title":"Default Title","offer_id":50503236485418,"sku":"BTS-B2016126","price":907.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0896\/1579\/4474\/files\/B2016126.png?v=1755359144"},{"product_id":"1-methyl-d-tryptophan","title":"1-Methyl-D-tryptophan","description":"\u003cdiv style=\"max-width: 1400px; margin: 0 auto; padding: 40px 20px; font-family: 'Open Sans', sans-serif; font-weight: 300; background: #fff; color: #333; font-size: 0.95rem; box-sizing: border-box;\"\u003e\n \u003cdiv style=\"display: flex; flex-direction: column; gap: 20px;\"\u003e\n \u003cp\u003e\u003cstrong\u003e1-Methyl-D-tryptophan\u003c\/strong\u003e\u003c\/p\u003e\n \u003cdiv style=\"overflow-x: auto; max-width: 100%; margin-bottom: 20px;\"\u003e\n \u003ctable style=\"width: 500px; border-collapse: collapse;\"\u003e\n \u003ctbody\u003e\n \u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eCatalog number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e B2016131\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eLot number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch Dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eExpiration Date:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eAmount:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 50 mg\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eMolecular Weight or Concentration:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 218.25\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eSupplied as:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Powder\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eApplications:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e a molecular tool for various biochemical applications\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eStorage:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e RT, Dry\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eKeywords:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e (2R)-2-Amino-3-(1-methyl-1H-indol-3-yl)propanoic acid, D-(+)-1-Methyltryptophan\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eGrade:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity \u0026gt;18 MΩ-cm) and are filtered through 0.22 um.\u003c\/td\u003e\n \u003c\/tr\u003e\n \u003c\/tbody\u003e\n \u003c\/table\u003e\n \u003c\/div\u003e\n\n \u003chr\u003e\n \u003ch4\u003eReferences\u003c\/h4\u003e\n \n \u003cul style=\"padding-left: 20px; margin: 0;\"\u003e\n \u003cli\u003eMatheus LHG, Dalmazzo SV, Brito RBO, Pereira LA, de Almeida RJ, Camacho CP, Dellê H. 1-Methyl-D-tryptophan activates aryl hydrocarbon receptor, a pathway associated with bladder cancer progression BMC Cancer. 2020 Sep 9;20(1):869.\u003c\/li\u003e\n\u003cli\u003eAlahdal M, Xing Y, Tang T, Liang J. 1-Methyl-D-tryptophan Reduces Tumor CD133(+) cells, Wnt\/β-catenin and NF-κβp65 while Enhances Lymphocytes NF-κβ2, STAT3, and STAT4 Pathways in Murine Pancreatic Adenocarcinoma Sci Rep. 2018 Jun 29;8(1):9869.\u003c\/li\u003e\n\u003cli\u003eJia L, Schweikart K, Tomaszewski J, Page JG, Noker PE, Buhrow SA, Reid JM, Ames MM, Munn DH. Toxicology and pharmacokinetics of 1-methyl-d-tryptophan: absence of toxicity due to saturating absorption Food Chem Toxicol. 2008 Jan;46(1):203-11.\u003c\/li\u003e\n\u003cli\u003eBrito RB, Malta CS, Souza DM, Matheus LH, Matos YS, Silva CS, Ferreira JM, Nunes VS, França CM, Dellê H. 1-Methyl-D-tryptophan potentiates TGF-β-induced epithelial-mesenchymal transition in T24 human bladder cancer cells PLoS One. 2015 Aug 12;10(8):e0134858.\u003c\/li\u003e\n\u003cli\u003eLiu Y, Xie J, Zhao X, Zhang Y, Zhong Z, Deng C. A polymeric IDO inhibitor based on poly(ethylene glycol)-b-poly(L-tyrosine-co-1-methyl-D_tryptophan) enables facile trident cancer immunotherapy Biomater Sci. 2022 Sep 27;10(19):5731-5743.\u003c\/li\u003e\n\u003cli\u003eOpitz CA, Litzenburger UM, Opitz U, Sahm F, Ochs K, Lutz C, Wick W, Platten M. The indoleamine-2,3-dioxygenase (IDO) inhibitor 1-methyl-D_tryptophan upregulates IDO1 in human cancer cells PLoS One. 2011;6(5):e19823.\u003c\/li\u003e\n\u003cli\u003eHuang GL, Tao A, Miyazaki T, Khan T, Hong T, Nakagawa Y, Cabral H. PEG-Poly(1-Methyl-l-Tryptophan)-Based Polymeric Micelles as Enzymatically Activated Inhibitors of Indoleamine 2,3-Dioxygenase Nanomaterials (Basel). 2019 May 9;9(5):719.\u003c\/li\u003e\n\u003cli\u003eCho T, Kok LY, Uetrecht J. Testing Possible Risk Factors for Idiosyncratic Drug-Induced Liver Injury Using an Amodiaquine Mouse Model and Co-treatment with 1-Methyl-d_Tryptophan or Acetaminophen ACS Omega. 2021 Feb 7;6(7):4656-4662.\u003c\/li\u003e\n\u003cli\u003eMetz R, Rust S, Duhadaway JB, Mautino MR, Munn DH, Vahanian NN, Link CJ, Prendergast GC. IDO inhibits a tryptophan sufficiency signal that stimulates mTOR: A novel IDO effector pathway targeted by D-1-methyl-tryptophan Oncoimmunology. 2012 Dec 1;1(9):1460-1468.\u003c\/li\u003e\n \u003c\/ul\u003e\n \u003c\/div\u003e\n \u003c\/div\u003e","brand":"Molecular Depot","offers":[{"title":"Default Title","offer_id":50503236616490,"sku":"BTS-B2016131","price":595.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0896\/1579\/4474\/files\/B2016131.png?v=1755359145"},{"product_id":"l-cysteic-acid-monohydrate","title":"L-Cysteic Acid Monohydrate","description":"\u003cdiv style=\"max-width: 1400px; margin: 0 auto; padding: 40px 20px; font-family: 'Open Sans', sans-serif; font-weight: 300; background: #fff; color: #333; font-size: 0.95rem; box-sizing: border-box;\"\u003e\n \u003cdiv style=\"display: flex; flex-direction: column; gap: 20px;\"\u003e\n \u003cp\u003e\u003cstrong\u003eL-Cysteic Acid Monohydrate\u003c\/strong\u003e\u003c\/p\u003e\n \u003cdiv style=\"overflow-x: auto; max-width: 100%; margin-bottom: 20px;\"\u003e\n \u003ctable style=\"width: 500px; border-collapse: collapse;\"\u003e\n \u003ctbody\u003e\n \u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eCatalog number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e B2016136\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eLot number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch Dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eExpiration Date:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eAmount:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 1 g\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eMolecular Weight or Concentration:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 187.17\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eSupplied as:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Powder\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eApplications:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e a molecular tool for various biochemical applications\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eStorage:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e RT, Dry\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eKeywords:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e (R)-2-Amino-3-sulfopropionic acid\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eGrade:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity \u0026gt;18 MΩ-cm) and are filtered through 0.22 um.\u003c\/td\u003e\n \u003c\/tr\u003e\n \u003c\/tbody\u003e\n \u003c\/table\u003e\n \u003c\/div\u003e\n\n \u003chr\u003e\n \u003ch4\u003eReferences\u003c\/h4\u003e\n \n \u003cul style=\"padding-left: 20px; margin: 0;\"\u003e\n \u003cli\u003eØhman KT, Sagstuen E. Free radical conformations and conversions in X-irradiated single crystals of L-cysteic acid by electron magnetic resonance and density functional theory studies J Phys Chem A. 2008 May 8;112(18):4284-93.\u003c\/li\u003e\n\u003cli\u003eDai Y, Wu G. Solid-State (17)O NMR Studies of Sulfonate Jump Dynamics in Crystalline Sulfonic Acids: Insights into the Hydrogen Bonding Effect J Phys Chem A. 2020 Nov 19;124(46):9597-9604.\u003c\/li\u003e\n\u003cli\u003eJohnstone RD, Lennie AR, Parsons S, Pidcock E, Warren JE. Comparison of the effects of pressure on three layered hydrates: a partially successful attempt to predict a high-pressure phase transition Acta Crystallogr B. 2009 Dec;65(Pt 6):731-48.\u003c\/li\u003e\n\u003cli\u003eBlaschko H. l(-)-Cysteic acid decarboxylase Biochem J. 1942 Sep;36(7-9):571-4.\u003c\/li\u003e\n\u003cli\u003eTao F, Luo Y, Wei Q, Zhang G. Efficient preparation of L-cysteic acid and its esters Amino Acids. 2004 Oct;27(2):149-51.\u003c\/li\u003e\n\u003cli\u003eLi XL, Yu J, Liu L. Poly[bis-(μ(7)-3-sulfonato-l-alaninato)sodiumzinc] Acta Crystallogr Sect E Struct Rep Online. 2012 Jun 1;68(Pt 6):m849.\u003c\/li\u003e\n\u003cli\u003eWu JY. Purification and characterization of cysteic acid and cysteine sulfinic acid decarboxylase and L-glutamate decarboxylase from bovine brain Proc Natl Acad Sci U S A. 1982 Jul;79(14):4270-4.\u003c\/li\u003e\n\u003cli\u003eRosowsky A, Forsch RA, Freisheim JH, Moran RG, Wick M. Methotrexate analogues. 19. Replacement of the glutamate side chain in classical antifolates by L-homocysteic acid and L-cysteic acid: effect on enzyme inhibition and antitumor activity J Med Chem. 1984 May;27(5):600-4.\u003c\/li\u003e\n\u003cli\u003eROBERTS CW, DU VIGNEAUD V. The synthesis of beta-sulfo-L-Alanyl-L-tyrosine and L-tyrosyl-L-cysteic acid and their dibromotyrosyl analogues J Biol Chem. 1953 Oct;204(2):871-5.\u003c\/li\u003e\n \u003c\/ul\u003e\n \u003c\/div\u003e\n \u003c\/div\u003e","brand":"Molecular Depot","offers":[{"title":"Default Title","offer_id":50503236780330,"sku":"BTS-B2016136","price":907.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0896\/1579\/4474\/files\/B2016136.png?v=1755359147"},{"product_id":"dl-phenylalanine-highly-pure","title":"DL-Phenylalanine (Highly Pure)","description":"\u003cdiv style=\"max-width: 1400px; margin: 0 auto; padding: 40px 20px; font-family: 'Open Sans', sans-serif; font-weight: 300; background: #fff; color: #333; font-size: 0.95rem; box-sizing: border-box;\"\u003e\n \u003cdiv style=\"display: flex; flex-direction: column; gap: 20px;\"\u003e\n \u003cp\u003e\u003cstrong\u003eDL-Phenylalanine (Highly Pure)\u003c\/strong\u003e\u003c\/p\u003e\n \u003cdiv style=\"overflow-x: auto; max-width: 100%; margin-bottom: 20px;\"\u003e\n \u003ctable style=\"width: 500px; border-collapse: collapse;\"\u003e\n \u003ctbody\u003e\n \u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eCatalog number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e B2016142\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eLot number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch Dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eExpiration Date:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eAmount:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 5 g\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eMolecular Weight or Concentration:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 165.19\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eSupplied as:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Powder\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eApplications:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e a molecular tool for various biochemical applications\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eStorage:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e RT, Dry\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eKeywords:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e (±)-2-Amino-3-phenylpropionic acid\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eGrade:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity \u0026gt;18 MΩ-cm) and are filtered through 0.22 um.\u003c\/td\u003e\n \u003c\/tr\u003e\n \u003c\/tbody\u003e\n \u003c\/table\u003e\n \u003c\/div\u003e\n\n \u003chr\u003e\n \u003ch4\u003eReferences\u003c\/h4\u003e\n \n \u003cul style=\"padding-left: 20px; margin: 0;\"\u003e\n \u003cli\u003eLi T, Fu B, Zhang X, Zhou Y, Yang M, Cao M, Chen Y, Tan Y, Hu R. Overproduction of Gastrointestinal 5-HT Promotes Colitis-Associated Colorectal Cancer Progression via Enhancing NLRP3 Inflammasome Activation Cancer Immunol Res. 2021 Sep;9(9):1008-1023.\u003c\/li\u003e\n\u003cli\u003eBeckmann H, Strauss MA, Ludolph E. Dl-phenylalanine in depressed patients: an open study J Neural Transm. 1977;41(2-3):123-34.\u003c\/li\u003e\n\u003cli\u003eLofft JG, Bridenbaugh RH. The availability of D-phenylalanine and DL-phenylalanine Am J Psychiatry. 1985 Feb;142(2):269-70.\u003c\/li\u003e\n\u003cli\u003eBeckmann H, Athen D, Olteanu M, Zimmer R. DL-phenylalanine versus imipramine: a double-blind controlled study Arch Psychiatr Nervenkr (1970). 1979 Jul 4;227(1):49-58.\u003c\/li\u003e\n\u003cli\u003eBai Y, Wang HM, Liu M, Wang Y, Lian GC, Zhang XH, Kang J, Wang HL. 4-Chloro-DL-phenylalanine protects against monocrotaline‑induced pulmonary vascular remodeling and lung inflammation Int J Mol Med. 2014 Feb;33(2):373-82.\u003c\/li\u003e\n\u003cli\u003eFirnau G, Nahmias C, Garnett S. Synthesis of 3,4-dihydroxy-5-fluoro-DL-phenylalanine and 3,4-dihydroxy-5-( 18 F)fluoro-DL-phenylalanine J Med Chem. 1973 Apr;16(4):416-8.\u003c\/li\u003e\n\u003cli\u003eRussell AL, McCarty MF. DL-phenylalanine markedly potentiates opiate analgesia – an example of nutrient\/pharmaceutical up-regulation of the endogenous analgesia system Med Hypotheses. 2000 Oct;55(4):283-8.\u003c\/li\u003e\n\u003cli\u003eKishore G, Sugumaran M, Vaidyanathan CS. Metabolism of DL-(+\/-)-phenylalanine by Aspergillus niger J Bacteriol. 1976 Oct;128(1):182-91.\u003c\/li\u003e\n\u003cli\u003eWood DR, Reimherr FW, Wender PH. Treatment of attention deficit disorder with DL-phenylalanine Psychiatry Res. 1985 Sep;16(1):21-6.\u003c\/li\u003e\n \u003c\/ul\u003e\n \u003c\/div\u003e\n \u003c\/div\u003e","brand":"Molecular Depot","offers":[{"title":"Default Title","offer_id":50503236944170,"sku":"BTS-B2016142","price":595.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0896\/1579\/4474\/files\/B2016142.png?v=1755359148"},{"product_id":"piperidine-solution","title":"Piperidine Solution","description":"\u003cdiv style=\"max-width: 1400px; margin: 0 auto; padding: 40px 20px; font-family: 'Open Sans', sans-serif; font-weight: 300; background: #fff; color: #333; font-size: 0.95rem; box-sizing: border-box;\"\u003e\n \u003cdiv style=\"display: flex; flex-direction: column; gap: 20px;\"\u003e\n \u003cp\u003e\u003cstrong\u003ePiperidine Solution\u003c\/strong\u003e\u003c\/p\u003e\n \u003cdiv style=\"overflow-x: auto; max-width: 100%; margin-bottom: 20px;\"\u003e\n \u003ctable style=\"width: 500px; border-collapse: collapse;\"\u003e\n \u003ctbody\u003e\n \u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eCatalog number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e B2016144\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eLot number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch Dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eExpiration Date:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eAmount:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 10 mL\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eMolecular Weight or Concentration:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 85.15\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eSupplied as:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Solution\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eApplications:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e a molecular tool for various biochemical applications\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eStorage:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e RT, Dry\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eKeywords:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Azacyclohexane, Cyclopentimine, Hexahydropyridine, Pentamethyleneimine\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eGrade:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity \u0026gt;18 MΩ-cm) and are filtered through 0.22 um.\u003c\/td\u003e\n \u003c\/tr\u003e\n \u003c\/tbody\u003e\n \u003c\/table\u003e\n \u003c\/div\u003e\n\n \u003chr\u003e\n \u003ch4\u003eReferences\u003c\/h4\u003e\n \n \u003cul style=\"padding-left: 20px; margin: 0;\"\u003e\n \u003cli\u003eHossein Mostafa D, Samadi A, Niknam S, Nasrollahi SA, Guishard A, Firooz A. Efficacy of Cetirizine 1% Versus Minoxidil 5% Topical Solution in the Treatment of Male Alopecia: A Randomized, Single-blind Controlled Study J Pharm Pharm Sci. 2021;24:191-199.\u003c\/li\u003e\n\u003cli\u003eRiviere JE. A novel long-acting transdermal fentanyl solution for dogs. Editorial J Vet Pharmacol Ther. 2012 Aug;35 Suppl 2:1.\u003c\/li\u003e\n\u003cli\u003ePayán MD, Li B, Petersen NJ, Jensen H, Hansen SH, Pedersen-Bjergaard S. Nano-electromembrane extraction Anal Chim Acta. 2013 Jun 27;785:60-6.\u003c\/li\u003e\n\u003cli\u003eGuerrier G, Boutboul D, Chanat C, Samama CM, Baillard C. Bicarbonate-buffered ropivacaine-mepivacaine solution for medial caruncle anaesthesia Anaesth Crit Care Pain Med. 2017 Aug;36(4):219-221.\u003c\/li\u003e\n\u003cli\u003eBECKETT AH, CASY AF, YOUSSEF HZ. DEMONSTRATION OF N-EPIMERS IN THE SALT OF A PIPERIDINE DERIVATIVE IN SOLUTION Tetrahedron Lett. 1965 Mar 10;10:537-42.\u003c\/li\u003e\n\u003cli\u003eAl-Hadedi AAM, Sawyer S, Elliott SJ, Green RA, O’Leary DJ, Brown RCD, Brown LJ. A flow electrochemistry-enabled synthesis of 2-substituted N-(methyl-d)piperidines J Labelled Comp Radiopharm. 2022 Dec;65(14):361-368.\u003c\/li\u003e\n\u003cli\u003eMangrum JB, Flora JW, Muddiman DC. Solution composition and thermal denaturation for the production of single-stranded PCR amplicons: piperidine-induced destabilization of the DNA duplex? J Am Soc Mass Spectrom. 2002 Mar;13(3):232-40.\u003c\/li\u003e\n\u003cli\u003eBlake DA, Fleischer CA, Wynn RL. Thalidomide solution Am J Obstet Gynecol. 1968 Dec 15;102(8):1179-80.\u003c\/li\u003e\n\u003cli\u003eTigoianu R, Airinei A, Georgescu E, Nicolescu A, Georgescu F, Isac DL, Deleanu C, Oancea F. Synthesis and Solvent Dependent Fluorescence of Some Piperidine-Substituted Naphthalimide Derivatives and Consequences for Water Sensing Int J Mol Sci. 2022 Mar 2;23(5):2760.\u003c\/li\u003e\n \u003c\/ul\u003e\n \u003c\/div\u003e\n \u003c\/div\u003e","brand":"Molecular Depot","offers":[{"title":"Default Title","offer_id":50503237075242,"sku":"BTS-B2016144","price":795.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0896\/1579\/4474\/files\/B2016144.png?v=1755359150"},{"product_id":"l-carnosine-highly-pure","title":"L-Carnosine (Highly Pure)","description":"\u003cdiv style=\"max-width: 1400px; margin: 0 auto; padding: 40px 20px; font-family: 'Open Sans', sans-serif; font-weight: 300; background: #fff; color: #333; font-size: 0.95rem; box-sizing: border-box;\"\u003e\n \u003cdiv style=\"display: flex; flex-direction: column; gap: 20px;\"\u003e\n \u003cp\u003e\u003cstrong\u003eL-Carnosine (Highly Pure)\u003c\/strong\u003e\u003c\/p\u003e\n \u003cdiv style=\"overflow-x: auto; max-width: 100%; margin-bottom: 20px;\"\u003e\n \u003ctable style=\"width: 500px; border-collapse: collapse;\"\u003e\n \u003ctbody\u003e\n \u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eCatalog number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e B2015890\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eLot number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch Dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eExpiration Date:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eAmount:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 10 g\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eMolecular Weight or Concentration:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 226.24 g\/mol\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eSupplied as:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Powder\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eApplications:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e a molecular tool for various biochemical applications\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eStorage:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 2-8°C\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eKeywords:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e H-β-Ala-His-OH; N-β-Alanyl-L-histidine\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eGrade:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity \u0026gt;18 MΩ-cm) and are filtered through 0.22 um.\u003c\/td\u003e\n \u003c\/tr\u003e\n \u003c\/tbody\u003e\n \u003c\/table\u003e\n \u003c\/div\u003e\n\n \u003chr\u003e\n \u003ch4\u003eReferences\u003c\/h4\u003e\n \n \u003cul style=\"padding-left: 20px; margin: 0;\"\u003e\n \u003cli\u003eBoldyrev AA, Aldini G, Derave W. Physiology and pathophysiology of carnosine Physiol Rev. 2013 Oct;93(4):1803-45.\u003c\/li\u003e\n\u003cli\u003eMenini S, Iacobini C, Fantauzzi CB, Pugliese G. L-carnosine and its Derivatives as New Therapeutic Agents for the Prevention and Treatment of Vascular Complications of Diabetes Curr Med Chem. 2020;27(11):1744-1763.\u003c\/li\u003e\n\u003cli\u003eCesak O, Vostalova J, Vidlar A, Bastlova P, Student V Jr. Carnosine and Beta-Alanine Supplementation in Human Medicine: Narrative Review and Critical Assessment Nutrients. 2023 Apr 5;15(7):1770.\u003c\/li\u003e\n\u003cli\u003eEfthymakis K, Neri M. The role of Zinc L-Carnosine in the prevention and treatment of gastrointestinal mucosal disease in humans: a review Clin Res Hepatol Gastroenterol. 2022 Aug-Sep;46(7):101954.\u003c\/li\u003e\n\u003cli\u003eAnn Abraham D, Muhasaparur Ganesan R. Effect of L-Carnosine on Children with ADHD Indian J Pediatr. 2022 Sep;89(9):935.\u003c\/li\u003e\n\u003cli\u003eAraminia B, Shalbafan M, Mortezaei A, Shirazi E, Ghaffari S, Sahebolzamani E, Mortazavi SH, Shariati B, Ardebili ME, Aqamolaei A, Naderi S, Akhondzadeh S. L-Carnosine combination therapy for major depressive disorder: A randomized, double-blind, placebo-controlled trial J Affect Disord. 2020 Apr 15;267:131-136.\u003c\/li\u003e\n\u003cli\u003eDarvishi B, Dinarvand R, Mohammadpour H, Kamarul T, Sharifi AM. Dual l-Carnosine\/Aloe vera Nanophytosomes with Synergistically Enhanced Protective Effects against Methylglyoxal-Induced Angiogenesis Impairment Mol Pharm. 2021 Sep 6;18(9):3302-3325.\u003c\/li\u003e\n\u003cli\u003eMousa AM, Aldebasi YH. L-carnosine mitigates interleukin-1α-induced dry eye disease in rabbits via its antioxidant, anti-inflammatory, antiapoptotic, and antifibrotic effects Cutan Ocul Toxicol. 2021 Sep;40(3):241-251.\u003c\/li\u003e\n\u003cli\u003eMatsukura T, Tanaka H. Applicability of zinc complex of L-carnosine for medical use Biochemistry (Mosc). 2000 Jul;65(7):817-23.\u003c\/li\u003e\n \u003c\/ul\u003e\n \u003c\/div\u003e\n \u003c\/div\u003e","brand":"Molecular Depot","offers":[{"title":"Default Title","offer_id":50503239401770,"sku":"BTS-B2015890","price":1167.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0896\/1579\/4474\/files\/B2015890.png?v=1755359249"},{"product_id":"l-lysyl-l-alanine-7-amido-4-methylcoumarin-dihydrochloride","title":"L-lysyl-L-alanine 7-amido-4-methylcoumarin Dihydrochloride","description":"\u003cdiv style=\"max-width: 1400px; margin: 0 auto; padding: 40px 20px; font-family: 'Open Sans', sans-serif; font-weight: 300; background: #fff; color: #333; font-size: 0.95rem; box-sizing: border-box;\"\u003e\n \u003cdiv style=\"display: flex; flex-direction: column; gap: 20px;\"\u003e\n \u003cp\u003e\u003cstrong\u003eL-lysyl-L-alanine 7-amido-4-methylcoumarin Dihydrochloride\u003c\/strong\u003e\u003c\/p\u003e\n \u003cdiv style=\"overflow-x: auto; max-width: 100%; margin-bottom: 20px;\"\u003e\n \u003ctable style=\"width: 500px; border-collapse: collapse;\"\u003e\n \u003ctbody\u003e\n \u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eCatalog number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e B2015901\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eLot number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch Dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eExpiration Date:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eAmount:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 50 mg\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eMolecular Weight or Concentration:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 447.36 g\/mol\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eSupplied as:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Powder\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eApplications:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e a molecular tool for various biochemical applications\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eStorage:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e -20 °C\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eKeywords:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Lys-Ala-7-amido-4-methylcoumarin Dihydrochloride\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eGrade:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity \u0026gt;18 MΩ-cm) and are filtered through 0.22 um.\u003c\/td\u003e\n \u003c\/tr\u003e\n \u003c\/tbody\u003e\n \u003c\/table\u003e\n \u003c\/div\u003e\n\n \u003chr\u003e\n \u003ch4\u003eReferences\u003c\/h4\u003e\n \n \u003cul style=\"padding-left: 20px; margin: 0;\"\u003e\n \u003cli\u003eZhu BW, Zhao LL, Sun LM, Li DM, Murata Y, Yu L, Zhang L. Purification and characterization of a cathepsin L-like enzyme from the body wall of the sea cucumber Stichopus japonicus Biosci Biotechnol Biochem. 2008 Jun;72(6):1430-7.\u003c\/li\u003e\n\u003cli\u003eLiu B, Traini R, Killinger B, Schneider B, Moszczynska A. Overexpression of parkin in the rat nigrostriatal dopamine system protects against methamphetamine neurotoxicity Exp Neurol. 2013 Sep;247:359-72.\u003c\/li\u003e\n\u003cli\u003eBolumar T, Sanz Y, Aristoy MC, Toldrá F. Purification and properties of an arginyl aminopeptidase from Debaryomyces hansenii Int J Food Microbiol. 2003 Sep 1;86(1-2):141-51.\u003c\/li\u003e\n\u003cli\u003eLai ML, Chen SW, Chen YH. Purification and characterization of a trypsin inhibitor from mouse seminal vesicle secretion Arch Biochem Biophys. 1991 Nov 1;290(2):265-71.\u003c\/li\u003e\n\u003cli\u003eDang LC, Melandri FD, Stein RL. Kinetic and mechanistic studies on the hydrolysis of ubiquitin C-terminal 7-amido-4-methylcoumarin by deubiquitinating enzymes Biochemistry. 1998 Feb 17;37(7):1868-79.\u003c\/li\u003e\n\u003cli\u003eSui L, Guo HC. Enhanced recombinant expression and purification of human IRAP for biochemical and crystallography studies Biochem Biophys Rep. 2021 Jun 9;27:101042.\u003c\/li\u003e\n\u003cli\u003eRahmani R, Debouba M, Aydi SS, Aydi S, Bouajila J. Comparative Analysis of Organic Extracts Bioactivity from Two Limonium. Mill Species Growing Wild in Tunisian Salty Marshes Chem Biodivers. 2023 Dec;20(12):e202301177.\u003c\/li\u003e\n\u003cli\u003eLiu Z, Zhao T, Li Z, Sun K, Fu Y, Cheng T, Guo J, Yu B, Shi X, Liu H. Discovery of [1,2,3]triazolo[4,5-d]pyrimidine derivatives as highly potent, selective, and cellularly active USP28 inhibitors Acta Pharm Sin B. 2020 Aug;10(8):1476-1491.\u003c\/li\u003e\n\u003cli\u003eZhu BW, Zhao LL, Sun LM, Li DM, Murata Y, Yu L, Zhang L. Purification and characterization of a cathepsin L-like enzyme from the body wall of the sea cucumber Stichopus japonicus Biosci Biotechnol Biochem. 2008 Jun;72(6):1430-7.\u003c\/li\u003e\n \u003c\/ul\u003e\n \u003c\/div\u003e\n \u003c\/div\u003e","brand":"Molecular Depot","offers":[{"title":"Default Title","offer_id":50503239565610,"sku":"BTS-B2015901","price":995.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0896\/1579\/4474\/files\/B2015901.png?v=1755359256"},{"product_id":"l-arginine-7-amido-4-methylcoumarin-dihydrochloride","title":"L-Arginine 7-amido-4-methylcoumarin Dihydrochloride","description":"\u003cdiv style=\"max-width: 1400px; margin: 0 auto; padding: 40px 20px; font-family: 'Open Sans', sans-serif; font-weight: 300; background: #fff; color: #333; font-size: 0.95rem; box-sizing: border-box;\"\u003e\n \u003cdiv style=\"display: flex; flex-direction: column; gap: 20px;\"\u003e\n \u003cp\u003e\u003cstrong\u003eL-Arginine 7-amido-4-methylcoumarin Dihydrochloride\u003c\/strong\u003e\u003c\/p\u003e\n \u003cdiv style=\"overflow-x: auto; max-width: 100%; margin-bottom: 20px;\"\u003e\n \u003ctable style=\"width: 500px; border-collapse: collapse;\"\u003e\n \u003ctbody\u003e\n \u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eCatalog number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e B2015910\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eLot number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch Dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eExpiration Date:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eAmount:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 100 mg\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eMolecular Weight or Concentration:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 404.30 g\/mol\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eSupplied as:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Powder\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eApplications:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e a molecular tool for various biochemical applications\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eStorage:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e -20 °C\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eKeywords:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e H-Arg-AMC·2HCl\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eGrade:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity \u0026gt;18 MΩ-cm) and are filtered through 0.22 um.\u003c\/td\u003e\n \u003c\/tr\u003e\n \u003c\/tbody\u003e\n \u003c\/table\u003e\n \u003c\/div\u003e\n\n \u003chr\u003e\n \u003ch4\u003eReferences\u003c\/h4\u003e\n \n \u003cul style=\"padding-left: 20px; margin: 0;\"\u003e\n \u003cli\u003eZhu BW, Zhao LL, Sun LM, Li DM, Murata Y, Yu L, Zhang L. Purification and characterization of a cathepsin L-like enzyme from the body wall of the sea cucumber Stichopus japonicus Biosci Biotechnol Biochem. 2008 Jun;72(6):1430-7.\u003c\/li\u003e\n\u003cli\u003eCuker A, Arepally GM, Chong BH, Cines DB, Greinacher A, Gruel Y, Linkins LA, Rodner SB, Selleng S, Warkentin TE, Wex A, Mustafa RA, Morgan RL, Santesso N. American Society of Hematology 2018 guidelines for management of venous thromboembolism: heparin-induced thrombocytopenia Blood Adv. 2018 Nov 27;2(22):3360-3392.\u003c\/li\u003e\n\u003cli\u003ePrince M, Wenham T. Heparin-induced thrombocytopaenia Postgrad Med J. 2018 Aug;94(1114):453-457.\u003c\/li\u003e\n\u003cli\u003eMozgovicz M, Fischer A, Brocard C, Jungbauer A, Lingg N. L-Arginine sulfate reduces irreversible protein binding in immobilized metal affinity chromatography J Chromatogr A. 2023 Sep 13;1706:464246.\u003c\/li\u003e\n\u003cli\u003eKaback HR. Transport Annu Rev Biochem. 1970;39:561-98.\u003c\/li\u003e\n\u003cli\u003eMoore ZE, Corcoran MA, Patton D. Nutritional interventions for treating foot ulcers in people with diabetes Cochrane Database Syst Rev. 2020 Jul 17;7(7):CD011378.\u003c\/li\u003e\n\u003cli\u003eRosenthal GA, Dahlman DL, Robinson GW. L-Arginine kinase from tobacco hornworm, Manduca sexta (L.). Purification, properties, and interaction with L-canavanine J Biol Chem. 1977 Jun 10;252(11):3679-83.\u003c\/li\u003e\n\u003cli\u003eTeixeira LRM, Castro Perez A, Lima Romero TR, Gama Duarte ID. Magnesium sulphate activates the L-arginine\/NO\/cGMP pathway to induce peripheral antinociception in mice Magnes Res. 2022 Jan 1;35(1):1-10.\u003c\/li\u003e\n\u003cli\u003eMedvidovic-Grubisic M, Stambolija V, Kolenc D, Katancic J, Murselovic T, Plestina-Borjan I, Strbe S, Drmic D, Barisic I, Sindic A, Seiwerth S, Sikiric P. Hypermagnesemia disturbances in rats, NO-related: pentadecapeptide BPC 157 abrogates, L-NAME and L-arginine worsen Inflammopharmacology. 2017 Aug;25(4):439-449.\u003c\/li\u003e\n \u003c\/ul\u003e\n \u003c\/div\u003e\n \u003c\/div\u003e","brand":"Molecular Depot","offers":[{"title":"Default Title","offer_id":50503239631146,"sku":"BTS-B2015910","price":795.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0896\/1579\/4474\/files\/B2015910.png?v=1755359259"},{"product_id":"nn-dimethylglycine","title":"N,N-Dimethylglycine","description":"\u003cdiv style=\"max-width: 1400px; margin: 0 auto; padding: 40px 20px; font-family: 'Open Sans', sans-serif; font-weight: 300; background: #fff; color: #333; font-size: 0.95rem; box-sizing: border-box;\"\u003e\n \u003cdiv style=\"display: flex; flex-direction: column; gap: 20px;\"\u003e\n \u003cp\u003e\u003cstrong\u003eN,N-Dimethylglycine\u003c\/strong\u003e\u003c\/p\u003e\n \u003cdiv style=\"overflow-x: auto; max-width: 100%; margin-bottom: 20px;\"\u003e\n \u003ctable style=\"width: 500px; border-collapse: collapse;\"\u003e\n \u003ctbody\u003e\n \u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eCatalog number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e B2015847\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eLot number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch Dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eExpiration Date:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eAmount:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 5 mg\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eMolecular Weight or Concentration:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 103.12\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eSupplied as:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Powder\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eApplications:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e a molecular tool for various biochemical applications\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eStorage:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e RT, dry\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eKeywords:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e (Dimethylamino)acetic acid\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eGrade:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity \u0026gt;18 MΩ-cm) and are filtered through 0.22 um.\u003c\/td\u003e\n \u003c\/tr\u003e\n \u003c\/tbody\u003e\n \u003c\/table\u003e\n \u003c\/div\u003e\n\n \u003chr\u003e\n \u003ch4\u003eReferences\u003c\/h4\u003e\n \n \u003cul style=\"padding-left: 20px; margin: 0;\"\u003e\n \u003cli\u003eDhanjal DS, Bhardwaj S, Chopra C, Singh R, Patocka J, Plucar B, Nepovimova E, Valis M, Kuca K. Millennium Nutrient N,N-Dimethylglycine (DMG) and its Effectiveness in Autism Spectrum Disorders Curr Med Chem. 2022;29(15):2632-2651.\u003c\/li\u003e\n\u003cli\u003eHerbert V. N,N-dimethylglycine_for epilepsy N Engl J Med. 1983 Mar 3;308(9):527-8.\u003c\/li\u003e\n\u003cli\u003eLever M, McEntyre CJ, George PM, Chambers ST. Is N,N-dimethylglycine_N-oxide a choline and betaine metabolite? Biol Chem. 2017 Jun 27;398(7):775-784.\u003c\/li\u003e\n\u003cli\u003eTonda ME, Hart LL. N,N dimethylglycine_and L-carnitine as performance enhancers in athletes Ann Pharmacother. 1992 Jul-Aug;26(7-8):935-7.\u003c\/li\u003e\n\u003cli\u003eYang T, Shao YH, Guo LZ, Meng XL, Yu H, Lu WD. Role of N,N-Dimethylglycine_and Its Catabolism to Sarcosine in Chromohalobacter salexigens DSM 3043 Appl Environ Microbiol. 2020 Aug 18;86(17):e01186-20.\u003c\/li\u003e\n\u003cli\u003eLendvai A, Béke G, Hollósi E, Becker M, Völker JM, Schulze Zur Wiesche E, Bácsi A, Bíró T, Mihály J. N,N-Dimethylglycine_Sodium Salt Exerts Marked Anti-Inflammatory Effects in Various Dermatitis Models and Activates Human Epidermal Keratinocytes by Increasing Proliferation, Migration, and Growth Factor Release Int J Mol Sci. 2023 Jul 9;24(14):11264.\u003c\/li\u003e\n\u003cli\u003eWolfsegger T, Böck K, Schimetta W, von Oertzen TJ, Assar H. N,N-Dimethylglycine in patients with progressive multiple sclerosis: result of a pilot double-blind, placebo, controlled randomized clinical trial Neurol Res Pract. 2021 May 24;3(1):29.\u003c\/li\u003e\n\u003cli\u003eGascon G, Patterson B, Yearwood K, Slotnick H. N,N dimethylglycine and epilepsy Epilepsia. 1989 Jan-Feb;30(1):90-3.\u003c\/li\u003e\n\u003cli\u003eFreed WJ. N,N-dimethylglycine, betaine, and seizures Arch Neurol. 1984 Nov;41(11):1129-30.\u003c\/li\u003e\n \u003c\/ul\u003e\n \u003c\/div\u003e\n \u003c\/div\u003e","brand":"Molecular Depot","offers":[{"title":"Default Title","offer_id":50503239794986,"sku":"BTS-B2015847","price":595.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0896\/1579\/4474\/files\/B2015847.png?v=1755359267"},{"product_id":"3-aminobenzoic-acid-highly-pure","title":"3-aminobenzoic Acid (Highly Pure)","description":"\u003cdiv style=\"max-width: 1400px; margin: 0 auto; padding: 40px 20px; font-family: 'Open Sans', sans-serif; font-weight: 300; background: #fff; color: #333; font-size: 0.95rem; box-sizing: border-box;\"\u003e\n \u003cdiv style=\"display: flex; flex-direction: column; gap: 20px;\"\u003e\n \u003cp\u003e\u003cstrong\u003e3-aminobenzoic Acid (Highly Pure)\u003c\/strong\u003e\u003c\/p\u003e\n \u003cdiv style=\"overflow-x: auto; max-width: 100%; margin-bottom: 20px;\"\u003e\n \u003ctable style=\"width: 500px; border-collapse: collapse;\"\u003e\n \u003ctbody\u003e\n \u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eCatalog number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e B2015853\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eLot number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch Dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eExpiration Date:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eAmount:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 5 g\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eMolecular Weight or Concentration:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 137.14\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eSupplied as:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Powder\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eApplications:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e a molecular tool for various biochemical applications\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eStorage:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e RT, dry\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eKeywords:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 3-aminobenzenecarboxylic acid, 3-Carboxyaniline, m-aminobenzoic acid, Aniline-3-carboxylic acid\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eGrade:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity \u0026gt;18 MΩ-cm) and are filtered through 0.22 um.\u003c\/td\u003e\n \u003c\/tr\u003e\n \u003c\/tbody\u003e\n \u003c\/table\u003e\n \u003c\/div\u003e\n\n \u003chr\u003e\n \u003ch4\u003eReferences\u003c\/h4\u003e\n \n \u003cul style=\"padding-left: 20px; margin: 0;\"\u003e\n \u003cli\u003eVasil’eva I, Morozova O, Shumakovich G, Yaropolov A. Betaine-Based Deep Eutectic Solvent as a New Media for Laccase-Catalyzed Template-Guided Polymerization\/Copolymerization of Aniline and 3-Aminobenzoic Acid Int J Mol Sci. 2022 Sep 27;23(19):11409.\u003c\/li\u003e\n\u003cli\u003eJeyaraman Selvaraj N, Sathya U, Gomathi S, Jegan Jennifer S, Mathivathanan L, Abdul Razak I. Synthesis, crystal structure determination and Hirshfeld surface analysis of three new salt forms of creatinine with hydrobromic acid, 3-aminobenzoic acid and 3,5-dinitrobenzoic acid Acta Crystallogr C Struct Chem. 2022 Aug 1;78(Pt 8):437-448.\u003c\/li\u003e\n\u003cli\u003eZhao S, Pan C, Zhao J, Du H, Li M, Yu H, Chen X. Quantitative proteomic analysis of the microbial degradation of 3-aminobenzoic acid by Comamonas sp. QT12 Sci Rep. 2022 Oct 20;12(1):17609.\u003c\/li\u003e\n\u003cli\u003eKudo F, Zhang J, Sato S, Hirayama A, Eguchi T. Functional Characterization of 3-Aminobenzoic Acid Adenylation Enzyme PctU and UDP-N-Acetyl-d-Glucosamine: 3-Aminobenzoyl-ACP Glycosyltransferase PctL in Pactamycin Biosynthesis Chembiochem. 2019 Oct 1;20(19):2458-2462.\u003c\/li\u003e\n\u003cli\u003eModibane KD, Waleng NJ, Ramohlola KE, Maponya TC, Monama GR, Makgopa K, Hato MJ. Poly(3-aminobenzoic acid) Decorated with Cobalt Zeolitic Benzimidazolate Framework for Electrochemical Production of Clean Hydrogen Polymers (Basel). 2020 Jul 16;12(7):1581.\u003c\/li\u003e\n\u003cli\u003eKakehi K, Funakubo T, Suzuki S, Oda Y, Kitada Y. 3-Aminobenzamide and 3-aminobenzoic acid, tags for capillary electrophoresis of complex carbohydrates with laser-induced fluorescent detection J Chromatogr A. 1999 Nov 26;863(2):205-18.\u003c\/li\u003e\n\u003cli\u003ePhetsang S, Jakmunee J, Mungkornasawakul P, Laocharoensuk R, Ounnunkad K. Sensitive amperometric biosensors for detection of glucose and cholesterol using a platinum\/reduced graphene oxide\/poly(3-aminobenzoic acid) film-modified screen-printed carbon electrode Bioelectrochemistry. 2019 Jun;127:125-135.\u003c\/li\u003e\n\u003cli\u003eBenke BP, Madhavan N. Active ion transporters from readily accessible acyclic octapeptides containing 3-aminobenzoic acid and alanine Chem Commun (Camb). 2013 Aug 25;49(66):7340-2.\u003c\/li\u003e\n\u003cli\u003ePeng F, She H, Wang Y, Xu L, Shan Y, Chang Y, Zhong X, Li R, Qiu W, Shu Y, Tan S. Decreased kynurenine in cerebrospinal fluid and potential role in neuromyelitis optica spectrum disorder J Neurochem. 2023 Apr;165(2):259-267.\u003c\/li\u003e\n \u003c\/ul\u003e\n \u003c\/div\u003e\n \u003c\/div\u003e","brand":"Molecular Depot","offers":[{"title":"Default Title","offer_id":50503239893290,"sku":"BTS-B2015853","price":595.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0896\/1579\/4474\/files\/B2015853.png?v=1755359272"},{"product_id":"l-2-aminobutyric-acid-highly-pure","title":"L-2-aminobutyric Acid (Highly Pure)","description":"\u003cdiv style=\"max-width: 1400px; margin: 0 auto; padding: 40px 20px; font-family: 'Open Sans', sans-serif; font-weight: 300; background: #fff; color: #333; font-size: 0.95rem; box-sizing: border-box;\"\u003e\n \u003cdiv style=\"display: flex; flex-direction: column; gap: 20px;\"\u003e\n \u003cp\u003e\u003cstrong\u003eL-2-aminobutyric Acid (Highly Pure)\u003c\/strong\u003e\u003c\/p\u003e\n \u003cdiv style=\"overflow-x: auto; max-width: 100%; margin-bottom: 20px;\"\u003e\n \u003ctable style=\"width: 500px; border-collapse: collapse;\"\u003e\n \u003ctbody\u003e\n \u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eCatalog number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e B2015854\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eLot number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch Dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eExpiration Date:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eAmount:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 250 mg\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eMolecular Weight or Concentration:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 103.12\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eSupplied as:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Powder\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eApplications:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e a molecular tool for various biochemical applications\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eStorage:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e RT, dry\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eKeywords:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e L-α-aminobutyric acid\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eGrade:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity \u0026gt;18 MΩ-cm) and are filtered through 0.22 um.\u003c\/td\u003e\n \u003c\/tr\u003e\n \u003c\/tbody\u003e\n \u003c\/table\u003e\n \u003c\/div\u003e\n\n \u003chr\u003e\n \u003ch4\u003eReferences\u003c\/h4\u003e\n \n \u003cul style=\"padding-left: 20px; margin: 0;\"\u003e\n \u003cli\u003eFu Y, Zhang J, Fu X, Xie Y, Ren H, Liu J, Chen X, Liu L. [Production of L-2-aminobutyric acid from L-threonine using a trienzyme cascade] Sheng Wu Gong Cheng Xue Bao. 2020 Apr 25;36(4):782-791.\u003c\/li\u003e\n\u003cli\u003eXu JM, Li JQ, Zhang B, Liu ZQ, Zheng YG. Fermentative production of the unnatural amino acid L-2-aminobutyric acid based on metabolic engineering Microb Cell Fact. 2019 Feb 28;18(1):43.\u003c\/li\u003e\n\u003cli\u003eZhang L, Xiao Y, Yang W, Hua C, Wang Y, Li J, Yang T. [Synthesis of L-2-aminobutyric acid by leucine dehydrogenase coupling with an NADH regeneration system] Sheng Wu Gong Cheng Xue Bao. 2020 May 25;36(5):992-1001.\u003c\/li\u003e\n\u003cli\u003eZhang Z, Liu Y, Zhao J, Li W, Hu R, Li X, Li A, Wang Y, Ma L. Active-site engineering of ω-transaminase from Ochrobactrum anthropi for preparation of L-2-aminobutyric acid BMC Biotechnol. 2021 Sep 25;21(1):55.\u003c\/li\u003e\n\u003cli\u003eIrino Y, Toh R, Nagao M, Mori T, Honjo T, Shinohara M, Tsuda S, Nakajima H, Satomi-Kobayashi S, Shinke T, Tanaka H, Ishida T, Miyata O, Hirata KI. 2-Aminobutyric acid modulates glutathione homeostasis in the myocardium Sci Rep. 2016 Nov 9;6:36749.\u003c\/li\u003e\n\u003cli\u003eWeber N, Hatsch A, Labagnere L, Heider H. Production of (S)-2-aminobutyric acid and (S)-2-aminobutanol in Saccharomyces cerevisiae Microb Cell Fact. 2017 Mar 23;16(1):51.\u003c\/li\u003e\n\u003cli\u003eChen J, Zhu R, Zhou J, Yang T, Zhang X, Xu M, Rao Z. Efficient single whole-cell biotransformation for L-2-aminobutyric acid production through engineering of leucine dehydrogenase combined with expression regulation Bioresour Technol. 2021 Apr;326:124665.\u003c\/li\u003e\n\u003cli\u003eXu JM, Cheng F, Fu FT, Hu HF, Zheng YG. Semi-Rational Engineering of Leucine Dehydrogenase for L-2-Aminobutyric Acid Production Appl Biochem Biotechnol. 2017 Jul;182(3):898-909.\u003c\/li\u003e\n\u003cli\u003eChen J, Xu M, Yang T, Zhang X, Shao M, Li H, Rao Z. [Rational design of the C-terminal Loop region of leucine dehydrogenase and cascade biosynthesis L-2-aminobutyric acid] Sheng Wu Gong Cheng Xue Bao. 2021 Dec 25;37(12):4254-4265.\u003c\/li\u003e\n \u003c\/ul\u003e\n \u003c\/div\u003e\n \u003c\/div\u003e","brand":"Molecular Depot","offers":[{"title":"Default Title","offer_id":50503239926058,"sku":"BTS-B2015854","price":907.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0896\/1579\/4474\/files\/B2015854.png?v=1755359274"},{"product_id":"2-aminoisobutyric-acid-highly-pure","title":"2-aminoisobutyric Acid (Highly Pure)","description":"\u003cdiv style=\"max-width: 1400px; margin: 0 auto; padding: 40px 20px; font-family: 'Open Sans', sans-serif; font-weight: 300; background: #fff; color: #333; font-size: 0.95rem; box-sizing: border-box;\"\u003e\n \u003cdiv style=\"display: flex; flex-direction: column; gap: 20px;\"\u003e\n \u003cp\u003e\u003cstrong\u003e2-aminoisobutyric Acid (Highly Pure)\u003c\/strong\u003e\u003c\/p\u003e\n \u003cdiv style=\"overflow-x: auto; max-width: 100%; margin-bottom: 20px;\"\u003e\n \u003ctable style=\"width: 500px; border-collapse: collapse;\"\u003e\n \u003ctbody\u003e\n \u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eCatalog number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e B2015863\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eLot number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch Dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eExpiration Date:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eAmount:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 5 g\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eMolecular Weight or Concentration:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 103.12\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eSupplied as:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Powder\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eApplications:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e a molecular tool for various biochemical applications\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eStorage:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e RT, dry\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eKeywords:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e α-Aminoisobutyric acid, 2-Methylalanine, Aib\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eGrade:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity \u0026gt;18 MΩ-cm) and are filtered through 0.22 um.\u003c\/td\u003e\n \u003c\/tr\u003e\n \u003c\/tbody\u003e\n \u003c\/table\u003e\n \u003c\/div\u003e\n\n \u003chr\u003e\n \u003ch4\u003eReferences\u003c\/h4\u003e\n \n \u003cul style=\"padding-left: 20px; margin: 0;\"\u003e\n \u003cli\u003eMisawa T , Ohoka N , Oba M , Yamashita H , Tanaka M , Naito M , Demizu Y . Development of 2-aminoisobutyric acid (Aib)-rich cell-penetrating foldamers for efficient siRNA delivery Chem Commun (Camb). 2019 Jul 2;55(54):7792-7795.\u003c\/li\u003e\n\u003cli\u003eDouša M. Quantification of 2-aminoisobutyric acid impurity in enzalutamide bulk drug substance using hydrophilic interaction chromatography with fluorescence detection J Pharm Biomed Anal. 2019 Feb 5;164:296-301.\u003c\/li\u003e\n\u003cli\u003eTsuchiya K, Numata K. Chemoenzymatic synthesis of polypeptides containing the unnatural amino acid 2-aminoisobutyric acid Chem Commun (Camb). 2017 Jun 29;53(53):7318-7321.\u003c\/li\u003e\n\u003cli\u003eBergesse JR, Rivarola VA, Balegno HF. Changes in 2-aminoisobutyric acid and cycloleucine uptake produced by 2,4-dichlorophenoxyacetic acid in Chinese hamster ovary cells Toxicol Lett. 1987 Apr;36(2):189-96.\u003c\/li\u003e\n\u003cli\u003eLau YT, Chen JK, Chen BS, Hsieh CC. Transport of 2-aminoisobutyric acid in cultured endothelial cells Biochim Biophys Acta. 1994 Aug 24;1194(1):118-22.\u003c\/li\u003e\n\u003cli\u003eMisra R, George G, Saseendran A, Raghothama S, Gopi HN. Ambidextrous α,γ-Hybrid Peptide Foldamers Chem Asian J. 2019 Dec 2;14(23):4408-4414.\u003c\/li\u003e\n\u003cli\u003eAlonso JL, Peña I, López JC, Alonso ER, Vaquero V. The Shape of the Simplest Non-proteinogenic Amino Acid α-Aminoisobutyric Acid (Aib) Chemistry. 2019 Feb 11;25(9):2288-2294.\u003c\/li\u003e\n\u003cli\u003eTsuji AB, Kato K, Sugyo A, Okada M, Sudo H, Yoshida C, Wakizaka H, Zhang MR, Saga T. Comparison of 2-amino-[3-¹¹C]isobutyric acid and 2-deoxy-2-[¹⁸F]fluoro-D-glucose in nude mice with xenografted tumors and acute inflammation Nucl Med Commun. 2012 Oct;33(10):1058-64.\u003c\/li\u003e\n\u003cli\u003eSchaider H, Haberkorn U, Berger MR, Oberdorfer F, Morr I, van Kaick G. Application of alpha-aminoisobutyric acid, L-methionine, thymidine and 2-fluoro-2-deoxy-D-glucose to monitor effects of chemotherapy in a human colon carcinoma cell line Eur J Nucl Med. 1996 Jan;23(1):55-60.\u003c\/li\u003e\n \u003c\/ul\u003e\n \u003c\/div\u003e\n \u003c\/div\u003e","brand":"Molecular Depot","offers":[{"title":"Default Title","offer_id":50503239991594,"sku":"BTS-B2015863","price":907.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0896\/1579\/4474\/files\/B2015863.png?v=1755359275"},{"product_id":"5-bromo-3-indoxyl-13-diacetate","title":"5-bromo-3-indoxyl-1,3-diacetate","description":"\u003cdiv style=\"max-width: 1400px; margin: 0 auto; padding: 40px 20px; font-family: 'Open Sans', sans-serif; font-weight: 300; background: #fff; color: #333; font-size: 0.95rem; box-sizing: border-box;\"\u003e\n \u003cdiv style=\"display: flex; flex-direction: column; gap: 20px;\"\u003e\n \u003cp\u003e\u003cstrong\u003e5-bromo-3-indoxyl-1,3-diacetate\u003c\/strong\u003e\u003c\/p\u003e\n \u003cdiv style=\"overflow-x: auto; max-width: 100%; margin-bottom: 20px;\"\u003e\n \u003ctable style=\"width: 500px; border-collapse: collapse;\"\u003e\n \u003ctbody\u003e\n \u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eCatalog number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e B2015865\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eLot number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch Dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eExpiration Date:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eAmount:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 5 g\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eMolecular Weight or Concentration:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 296.12 g\/mol\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eSupplied as:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Powder\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eApplications:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e a molecular tool for various biochemical applications\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eStorage:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e -20 °C\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eKeywords:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 5-bromo-3-indoxyl-1,3-diacetate\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eGrade:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity \u0026gt;18 MΩ-cm) and are filtered through 0.22 um.\u003c\/td\u003e\n \u003c\/tr\u003e\n \u003c\/tbody\u003e\n \u003c\/table\u003e\n \u003c\/div\u003e\n\n \u003chr\u003e\n \u003ch4\u003eReferences\u003c\/h4\u003e\n \n \u003cul style=\"padding-left: 20px; margin: 0;\"\u003e\n \u003cli\u003eAfrakssou Z, Rodi YK, Saffon N, Essassi el M, Ng SW. Di-tert-butyl 2,6,11-trioxo-2,3-dihydro-1H-anthra[1,2-d]imidazole-1,3-diacetate Acta Crystallogr Sect E Struct Rep Online. 2011 Jul 1;67(Pt 7):o1730.\u003c\/li\u003e\n\u003cli\u003eAfrakssou Z, Haoudi A, Capet F, Rolando C, El Ammari L. Diethyl 2,6,11-trioxo-2,3-dihydro-1H-anthra[1,2-d]imidazole-1,3-diacetate Acta Crystallogr Sect E Struct Rep Online. 2011 Aug 1;67(Pt 8):o2081.\u003c\/li\u003e\n\u003cli\u003eLee JH, Kim TH, Kim HS, Kim AR, Kim DK, Nam ST, Kim HW, Park YH, Her E, Park YM, Kim HS, Kim YM, Choi WS. An indoxyl compound 5-bromo-4-chloro-3-indolyl 1,3-diacetate, CAC-0982, suppresses activation of Fyn kinase in mast cells and IgE-mediated allergic responses in mice Toxicol Appl Pharmacol. 2015 Jun 15;285(3):179-86.\u003c\/li\u003e\n\u003cli\u003eLian HC, Ni QL, Jiang XF, Cen ZM, Lin JH. Tetra-aqua-bis(2-methyl-benzimidazolium-1,3-diacetato-κO)zinc(II) tetra-hydrate Acta Crystallogr Sect E Struct Rep Online. 2009 Aug 19;65(Pt 9):m1091.\u003c\/li\u003e\n\u003cli\u003eFeng XL, Zhang YP. Tetra-aqua-bis-(2-methyl-1H-benzimidazolium-1,3-diacetato-κO)cobalt(II) tetra-hydrate Acta Crystallogr Sect E Struct Rep Online. 2011 Sep 1;67(Pt 9):m1170.\u003c\/li\u003e\n\u003cli\u003eElshamy AI, El-Kashak WA, Abdallah HM, Farrag AH, Nassar MI. Soft coral Cespitularia stolonifera: New cytotoxic ceramides and gastroprotective activity Chin J Nat Med. 2017 Feb;15(2):105-114.\u003c\/li\u003e\n\u003cli\u003eShannon WM, Westbrook L, Higuchi WI, Sugibayashi K, Baker DC, Kumar SD, Fox JL, Flynn GL, Ho NF, Vaidyanathan R. Influence of 1-dodecylazacycloheptan-2-one (Azone) on the topical therapy of cutaneous herpes simplex virus type 1 infection in hairless mice with 2′,3′-di-O-acetyl-9-beta-D-arabinofuranosyladenine and 5′-O-valeryl-9-beta-D-arabinofuranosyladenine J Pharm Sci. 1985 Nov;74(11):1157-61.\u003c\/li\u003e\n\u003cli\u003eGiner JL, Ferris WV Jr. Synthesis of 2-C-methyl-D-erythritol 2,4-cyclopyrophosphate Org Lett. 2002 Apr 4;4(7):1225-6.\u003c\/li\u003e\n\u003cli\u003eWallace PA, Minnikin DE. Synthesis of 4,6:2′,3′:4′,6′-tri-O-cyclohexylidene-alpha,alpha’-trehalose 2-palmitate: an intermediate for the synthesis of mycobacterial 2,3-di-O-acyl-alpha,alpha’-trehalose antigens Carbohydr Res. 1994 Oct 3;263(1):43-59.\u003c\/li\u003e\n \u003c\/ul\u003e\n \u003c\/div\u003e\n \u003c\/div\u003e","brand":"Molecular Depot","offers":[{"title":"Default Title","offer_id":50503240024362,"sku":"BTS-B2015865","price":1195.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0896\/1579\/4474\/files\/B2015865.png?v=1755359276"},{"product_id":"benzotriazol-1-yloxytripyrrolidinophosphonium-hexafluorophosphate","title":"(Benzotriazol-1-yloxy)tripyrrolidinophosphonium Hexafluorophosphate","description":"\u003cdiv style=\"max-width: 1400px; margin: 0 auto; padding: 40px 20px; font-family: 'Open Sans', sans-serif; font-weight: 300; background: #fff; color: #333; font-size: 0.95rem; box-sizing: border-box;\"\u003e\n \u003cdiv style=\"display: flex; flex-direction: column; gap: 20px;\"\u003e\n \u003cp\u003e\u003cstrong\u003e(Benzotriazol-1-yloxy)tripyrrolidinophosphonium Hexafluorophosphate\u003c\/strong\u003e\u003c\/p\u003e\n \u003cdiv style=\"overflow-x: auto; max-width: 100%; margin-bottom: 20px;\"\u003e\n \u003ctable style=\"width: 500px; border-collapse: collapse;\"\u003e\n \u003ctbody\u003e\n \u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eCatalog number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e B2015866\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eLot number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch Dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eExpiration Date:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eAmount:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 250 mg\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eMolecular Weight or Concentration:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 520.39\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eSupplied as:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Powder\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eApplications:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e a molecular tool for various biochemical applications\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eStorage:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 2-8°C\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eKeywords:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e PyBOP®\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eGrade:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity \u0026gt;18 MΩ-cm) and are filtered through 0.22 um.\u003c\/td\u003e\n \u003c\/tr\u003e\n \u003c\/tbody\u003e\n \u003c\/table\u003e\n \u003c\/div\u003e\n\n \u003chr\u003e\n \u003ch4\u003eReferences\u003c\/h4\u003e\n \n \u003cul style=\"padding-left: 20px; margin: 0;\"\u003e\n \u003cli\u003eSantos Oliveira AJM, de Castro RD, Pessôa HLF, Wadood A, de Sousa DP. Amides Derived from Vanillic Acid: Coupling Reactions, Antimicrobial Evaluation, and Molecular Docking Biomed Res Int. 2019 Apr 15;2019:9209676.\u003c\/li\u003e\n\u003cli\u003eFauconnot L, Robert F, Villard R, Dionisi F. Chemical synthesis and NMR characterization of structured polyunsaturated triacylglycerols Chem Phys Lipids. 2006 Feb;139(2):125-36.\u003c\/li\u003e\n\u003cli\u003eAkula HK, Lakshman MK. Facile Modifications at the C4 Position of Pyrimidine Nucleosides via In Situ Amide Activation with 1H-Benzotriazol-1-yloxy-tris(dimethyl-amino)phosphonium Hexafluorophosphate Curr Protoc Nucleic Acid Chem. 2019 Mar;76(1):e73.\u003c\/li\u003e\n\u003cli\u003eAkula HK, Kokatla H, Andrei G, Snoeck R, Schols D, Balzarini J, Yang L, Lakshman MK. Facile functionalization at the C4 position of pyrimidine nucleosides via amide group activation with (benzotriazol-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate (BOP) and biological evaluations of the products Org Biomol Chem. 2017 Feb 1;15(5):1130-1139.\u003c\/li\u003e\n\u003cli\u003eLi P, Xu JC. (1H-benzotriazol-1-yloxy)-N,N-dimethylmethaniminium hexachloroantimonate (BOMI), a novel coupling reagent for solution and solid-phase peptide synthesis J Pept Res. 2000 Feb;55(2):110-9.\u003c\/li\u003e\n\u003cli\u003eBae S, Lakshman MK. O6-(benzotriazol-1-yl)inosine derivatives: easily synthesized, reactive nucleosides J Am Chem Soc. 2007 Jan 31;129(4):782-9.\u003c\/li\u003e\n\u003cli\u003eAkula HK, Kokatla H, Andrei G, Snoeck R, Schols D, Balzarini J, Yang L, Lakshman MK. Correction: Facile functionalization at the C4 position of pyrimidine nucleosides via amide group activation with (benzotriazol-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate (BOP) and biological evaluations of the products Org Biomol Chem. 2017 Feb 1;15(5):1268.\u003c\/li\u003e\n\u003cli\u003eKhandaker TA, Hess JD, Aguilera R, Andrei G, Snoeck R, Schols D, Pradhan P, Lakshman MK. Synthesis and Evaluations of “1,4-Triazolyl Combretacoumarins” and Desmethoxy Analogues European J Org Chem. 2019 Sep 8;2019(33):5610-5623.\u003c\/li\u003e\n\u003cli\u003eKokatla HP, Lakshman MK. Two-step, one-pot synthesis of inosine, guanosine, and 2′-deoxyguanosine O6-ethers via intermediate O6-(benzotriazol-1-yl) derivatives Curr Protoc Nucleic Acid Chem. 2012 Jun;Chapter 1:Unit1.26.\u003c\/li\u003e\n \u003c\/ul\u003e\n \u003c\/div\u003e\n \u003c\/div\u003e","brand":"Molecular Depot","offers":[{"title":"Default Title","offer_id":50503240057130,"sku":"BTS-B2015866","price":595.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0896\/1579\/4474\/files\/B2015866.png?v=1755359278"},{"product_id":"2-ethoxy-1-ethoxycarbonyl-12-dihydroquinoline","title":"2-ethoxy-1-ethoxycarbonyl-1,2-dihydroquinoline","description":"\u003cdiv style=\"max-width: 1400px; margin: 0 auto; padding: 40px 20px; font-family: 'Open Sans', sans-serif; font-weight: 300; background: #fff; color: #333; font-size: 0.95rem; box-sizing: border-box;\"\u003e\n \u003cdiv style=\"display: flex; flex-direction: column; gap: 20px;\"\u003e\n \u003cp\u003e\u003cstrong\u003e2-ethoxy-1-ethoxycarbonyl-1,2-dihydroquinoline\u003c\/strong\u003e\u003c\/p\u003e\n \u003cdiv style=\"overflow-x: auto; max-width: 100%; margin-bottom: 20px;\"\u003e\n \u003ctable style=\"width: 500px; border-collapse: collapse;\"\u003e\n \u003ctbody\u003e\n \u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eCatalog number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e B2015869\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eLot number:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch Dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eExpiration Date:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Batch dependent\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eAmount:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 1 g\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eMolecular Weight or Concentration:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 247.29\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eSupplied as:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Powder\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eApplications:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e a molecular tool for various biochemical applications\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eStorage:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e 2-8°C\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eKeywords:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e N-Ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline, EEDQ, Ethyl 1,2-dihydro-2-ethoxyquinoline-1-carboxylate\u003c\/td\u003e\n \u003c\/tr\u003e\n\u003ctr style=\"border-bottom: 1px solid #ddd;\"\u003e\n \u003ctd style=\"width: 150px; padding-right: 10px;\"\u003e\u003cstrong\u003eGrade:\u003c\/strong\u003e\u003c\/td\u003e\n \u003ctd style=\"width: 350px;\"\u003e Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity \u0026gt;18 MΩ-cm) and are filtered through 0.22 um.\u003c\/td\u003e\n \u003c\/tr\u003e\n \u003c\/tbody\u003e\n \u003c\/table\u003e\n \u003c\/div\u003e\n\n \u003chr\u003e\n \u003ch4\u003eReferences\u003c\/h4\u003e\n \n \u003cul style=\"padding-left: 20px; margin: 0;\"\u003e\n \u003cli\u003eMeller E, Goldstein M, Friedhoff AJ, Schweitzer JW. N-ethoxycarbonyl-2-ethoxy-1,_2-dihydroquinoline_(EEDQ): a new tool to probe CNS receptor function Adv Exp Med Biol. 1988;235:121-36.\u003c\/li\u003e\n\u003cli\u003eSánchez C, Mørk A. N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline_studies on the role of 5-HT1A and 5-HT2 receptors in mediating foot-shock-induced ultrasonic vocalisation in adult rats Eur Neuropsychopharmacol. 1999 Jun;9(4):287-94.\u003c\/li\u003e\n\u003cli\u003eGnanalingham KK, Hunter AJ, Jenner P, Marsden CD. An autoradiographic study of the differential effects of N-ethoxycarbonyl-2-ethoxy-1,_2-dihydroquinoline_(EEDQ) on striatal and extrastriatal D-1 and D-2 dopamine receptors in the rat Neuropharmacology. 1994 May;33(5):647-55.\u003c\/li\u003e\n\u003cli\u003eSteverding D, Kadenbach B. Influence of N-ethoxycarbonyl-2-ethoxy-1,_2-dihydroquinoline_modification on proton translocation and membrane potential of reconstituted cytochrome-c oxidase support “proton slippage” J Biol Chem. 1991 May 5;266(13):8097-101.\u003c\/li\u003e\n\u003cli\u003eSaller CF, Kreamer LD, Adamovage LA, Salama AI. Dopamine receptor occupancy in vivo: measurement using N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline_(EEDQ) Life Sci. 1989;45(10):917-29.\u003c\/li\u003e\n\u003cli\u003eMiralles A, Ribas C, Olmos G, García-Sevilla JA. Differential effects of the alkylating agent N-ethoxycarbonyl-2- ethoxy-1, 2-dihydroquinoline_on brain alpha 2-adrenoceptors and I2-imidazoline sites in vitro and in vivo J Neurochem. 1993 Nov;61(5):1602-10.\u003c\/li\u003e\n\u003cli\u003eRocco VK, Cragoe EJ Jr, Warnock DG. N-ethoxycarbonyl-2ethoxy-1,2-dihydroquinoline, amiloride analogues, and renal Na+\/H+ antiporter Am J Physiol. 1987 Mar;252(3 Pt 2):F517-24.\u003c\/li\u003e\n\u003cli\u003eAdler CH, Meller E, Goldstein M. Recovery of alpha 2-adrenoceptor binding and function after irreversible inactivation by N-ethoxycarbonyl-2-ethoxy-1, 2-dihydroquinoline_(EEDQ) Eur J Pharmacol. 1985 Oct 8;116(1-2):175-8.\u003c\/li\u003e\n\u003cli\u003eChiu AT, Wong PC, Timmermans PB. Alpha-1 adrenoceptor-induced Ca++ movements in rat aorta: antagonism by phenoxybenzamine and N-ethoxycarbonyl-2-ethoxy-1, 2-dihydroquinoline_J Pharmacol Exp Ther. 1987 Nov;243(2):577-83.\u003c\/li\u003e\n \u003c\/ul\u003e\n \u003c\/div\u003e\n \u003c\/div\u003e","brand":"Molecular Depot","offers":[{"title":"Default Title","offer_id":50503240089898,"sku":"BTS-B2015869","price":595.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0896\/1579\/4474\/files\/B2015869.png?v=1755359280"}],"url":"https:\/\/bluetigerscientific.com\/collections\/organic-synthesis.oembed","provider":"Blue Tiger Scientific","version":"1.0","type":"link"}