Molecular Formula | C25H21F3N2O |
Molar Mass | 422.45 |
Solubility | soluble in DMSO, not in water |
Storage Condition | -20℃ |
Use | Mavatrep is an orally bioeffective TRPV1 antagonist with high affinity for hTRPV1 channels, inhibiting the binding of TRPV1 agonists to [3H]-Resiniferatoxin (Ki = 6.5 nM), and less effective on the enzymatic activities of CYP subtypes 3A4, 1A2, and 2D6. |
Reference Show more | Parsons WH, et al. Benzo[d]imidazole Transient Receptor Potential Vanilloid 1 Antagonists for the Treatment of Pain: Discovery of trans-2-(2-{2-[2-(4-Trifluoromethyl-phenyl)-vinyl]-1H-benzimidazol-5-yl}-phenyl)-propan-2-ol (Mavatrep). J Med Chem. 2015 May 14;58(9):3859-3874. |
1mg | 5mg | 10mg | |
---|---|---|---|
1 mM | 2.367 ml | 11.836 ml | 23.672 ml |
5 mM | 0.473 ml | 2.367 ml | 4.734 ml |
10 mM | 0.237 ml | 1.184 ml | 2.367 ml |
5 mM | 0.047 ml | 0.237 ml | 0.473 ml |