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Eplivanserin hemifumarate

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Catalog No. T27277Cas No. 130580-02-8
Alias SR-46349 Fumarate, SR46349 Fumarate, SR 46349 Fumarate, Eplivanserin fumarate

Eplivanserin is an inverse agonist of 5-HT2A.

Eplivanserin hemifumarate

Eplivanserin hemifumarate

😃Good
Catalog No. T27277Alias SR-46349 Fumarate, SR46349 Fumarate, SR 46349 Fumarate, Eplivanserin fumarateCas No. 130580-02-8
Eplivanserin is an inverse agonist of 5-HT2A.
Pack SizePriceAvailabilityQuantity
2 mg$1215 days
50 mg$7876-8 weeks
100 mg$1,1906-8 weeks
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Product Introduction

Bioactivity
Description
Eplivanserin is an inverse agonist of 5-HT2A.
Targets&IC50
5-HT2C receptor:120 nM (IC50), 5-HT2A receptor:5.8 nM (IC50)
AliasSR-46349 Fumarate, SR46349 Fumarate, SR 46349 Fumarate, Eplivanserin fumarate
Chemical Properties
Molecular Weight444.45
FormulaC23H25FN2O6
Cas No.130580-02-8
Relative Density.no data available
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.

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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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