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6-Methoxygramine (Highly Pure) Chemicals Molecular Depot
6-Methoxygramine (Highly Pure) Chemicals Molecular Depot
6-Methoxygramine (Highly Pure) Chemicals Molecular Depot
6-Methoxygramine (Highly Pure) Chemicals Molecular Depot

6-Methoxygramine (Highly Pure)

$1,395.00

    Catalog Number: B2016558 (1 g)

    6-Methoxygramine (Highly Pure) is a high quality chemical compound that belongs to the class of alkaloids. It is a derivative of gramine, which is a naturally occurring alkaloid found in certain plants. This product has been used as a molecular tool for various biochemical applications. It has also been used in a wide array of other chemical and immunological applications. Custom bulk amounts of this product are available upon request.

    Products are for in vitro research use only (RUO).

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What's Included

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VR Headset

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2 Touch Controllers

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Charging Cable

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Power Adapter

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Glasses Spacer

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6-Methoxygramine (Highly Pure)

Catalog number: B2016558
Lot number: Batch Dependent
Expiration Date: Batch dependent
Amount: 1 g
Molecular Weight or Concentration: 204.27 g/mol
Supplied as: Powder
Applications: a molecular tool for various biochemical applications
Storage: 2-8°C
Keywords: 3-(Dimethylaminomethyl)-6-methoxyindole
Grade: Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity >18 MΩ-cm) and are filtered through 0.22 um.

References

  • Koroša A, Mali N. Control of organic contaminants in groundwater by passive sampling and multivariate statistical analysis J Environ Manage. 2022 Sep 15;318:115440.
  • Gerschenfeld HM, Paupardin-Tritsch D. On the transmitter function of 5-hydroxytryptamine at excitatory and inhibitory monosynaptic junctions J Physiol. 1974 Dec;243(2):457-81.
  • Schlag BD, Lou Z, Fennell M, Dunlop J. Ligand dependency of 5-hydroxytryptamine 2C receptor internalization J Pharmacol Exp Ther. 2004 Sep;310(3):865-70.
  • Clancy BM, Osman R, Maayani S. Kinetics of competitive drug action at 5-hydroxytryptamine2 receptors in isolated rabbit aorta J Pharmacol Exp Ther. 1987 Jul;242(1):108-14.
  • Stollak JS, Furchgott RF. Use of selective antagonists for determining the types of receptors mediating the actions of 5-hydroxytryptamine and tryptamine in the isolated rabbit aorta J Pharmacol Exp Ther. 1983 Jan;224(1):215-21.
  • Gerschenfeld HM, Paupardin-Tritsch D. Ionic mechanisms and receptor properties underlying the responses of molluscan neurones to 5-hydroxytryptamine J Physiol. 1974 Dec;243(2):427-56.
  • Devlin MG, Smith NJ, Ryan OM, Guida E, Sexton PM, Christopoulos A. Regulation of serotonin 5-HT2C receptors by chronic ligand exposure Eur J Pharmacol. 2004 Sep 13;498(1-3):59-69.
  • Oshita M, Kigoshi S, Muramatsu I. Contractile action of yohimbine in the dog basilar artery Blood Vessels. 1985;22(6):257-64.
  • Addala E, Rafiei H, Das S, Bandy B, Das U, Karki SS, Dimmock JR. 3,5-Bis(3-dimethylaminomethyl-4-hydroxybenzylidene)-4-piperidone and related compounds induce glutathione oxidation and mitochondria-mediated cell death in HCT-116 colon cancer cells Bioorg Med Chem Lett. 2017 Aug 15;27(16):3669-3673.

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Product Resources:

Copy of Technical Specifications

FeatureDetails
Viewing Head Siedentopf type trinocular head, inclined at 30°, Interpupillary adjustment 53mm to 75mm, graduated diopter on left eyetube (30mm I.D. eyetubes)
Eyepieces SWH10X Widefield high eyepoint eyepiece, Field No. 22, tube O.D. 30.0 mm
Nosepiece Quintuple
Quintuple LWD Planachromat Phase 10x, 20x
Condenser TC Condenser N.A. 0.30, W.D. 73.0mm
Stage180mm(X) x 245mm(Y) plain stage with replaceable glass insert with 45mm opening, Glass Stage plate insert
IlluminationKoehler without iris, with phase slider, 3W LED
WarrantyLIMITED LIFETIME WARRANTY

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