AMG 9810
Tocris Bioscience, part of Bio-Techne | Catalog # 2316
Potent and selective TRPV1 competitive antagonist
Key Product Details
Description
Potent and selective TRPV1 competitive antagonist
Product Description
AMG 9810 is a potent and selective, competitive vanilloid TRPV1 receptor antagonist (IC50 = 17 nM). Inhibits capsaicin-, proton-, heat- and endogenous ligand-induced activation of human and rat recombinant TRPV1 receptors. Displays antihyperalgesic properties in a rat model of inflammatory pain.Product Specifications
Molecular Weight
337.42
Formula
C21H23NO3
Storage
Store at +4°C
Purity
≥98% (HPLC)
Chemical Name
(2E)-N-(2,3-Dihydro-1,4-benzodioxin-6-yl)-3-[4-(1,1-dimethylethyl)phenyl]-2-propenamide
CAS Number
545395-94-6
PubChem ID
680502
InChI Key
GZTFUVZVLYUPRG-IZZDOVSWSA-N
SMILES
CC(C)(C)C1=CC=C(C=C1)\C=C\C(=O)NC1=CC=C2OCCOC2=C1
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
Solubility
| Solvent | Max Conc. mg/mL | Max Conc. mM | |
|---|---|---|---|
| Solubility | |||
| DMSO | 16.87 | 50 | |
| Ethanol | 33.74 | 100 |
Preparing Stock Solutions
for AMG 9810
The following data is based on the product molecular weight 337.42
Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which all affect the solvent volumes required to prepare stock solutions.
| Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
|---|---|---|---|
| 1 mM | 2.96 mL | 14.82 mL | 29.64 mL |
| 5 mM | 0.59 mL | 2.96 mL | 5.93 mL |
| 10 mM | 0.30 mL | 1.48 mL | 2.96 mL |
| 50 mM | 0.06 mL | 0.30 mL | 0.59 mL |
Calculators
Molarity Calculator
Dilution Calculator
Reconstitution Calculator
Background References
References are publications that support the biological activity of the product.
- Gavva AMG 9810 [(E)-3-(4-t-Butylphenyl)-N-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)acrylamide], a novel vanilloid receptor 1 (TRPV1) antagonist with antihyperalgesic properties. J.Pharmacol.Exp.Ther. 2005 PMID: 15615864
- Mouchbahani-Constance Lionfish venom elicits pain predominantly through the activation of nonpeptidergic nociceptors. Pain. 2018 PMID: 29965829
- Doherty Discovery of potent, orally available vanilloid receptor-1 antagonists. Structure-activity relationship of N-aryl cinnamides. J.Med.Chem. 2005 PMID: 15634002
Product Specific Notices for AMG 9810
For research use only
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