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AMPA receptor antagonist-2

Catalog No. T61068Cas No. 732277-05-3

AMPA receptor antagonist-2 is an AMPA receptor antagonist.

AMPA receptor antagonist-2

AMPA receptor antagonist-2

Purity: 98.21%
Catalog No. T61068Cas No. 732277-05-3
AMPA receptor antagonist-2 is an AMPA receptor antagonist.
Pack SizePriceAvailabilityQuantity
1 mg$117In Stock
5 mg$269In Stock
10 mg$395In Stock
25 mg$592In Stock
50 mg$834In Stock
100 mg$1,120In Stock
1 mL x 10 mM (in DMSO)$268In Stock
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Purity:98.21%
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Product Introduction

Bioactivity
Description
AMPA receptor antagonist-2 is an AMPA receptor antagonist.
Chemical Properties
Molecular Weight339.35
FormulaC18H17N3O4
Cas No.732277-05-3
Storage & Solubility Information
StorageShipping with blue ice.
Solubility Information
DMSO: 11 mg/mL (32.41 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.9468 mL14.7341 mL29.4681 mL147.3405 mL
5 mM0.5894 mL2.9468 mL5.8936 mL29.4681 mL
10 mM0.2947 mL1.4734 mL2.9468 mL14.7341 mL
20 mM0.1473 mL0.7367 mL1.4734 mL7.3670 mL

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Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% ddH2O. So your working solution concentration is 2 mg/mL。
Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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