Description
A TRPV4 antagonist (IC50s = 0.42 and 0.66 μM, respectively, for human and rat receptors); selective for TRPV4 over TRPV1, TRPV3, and TRPM8 (IC50s = 10, >30, and 30 μM, respectively); reduces 4α-PDD or hypotonicity-induced rat TRPV4 activity (IC50s = 0.57 and 2.1 μM, respectively, in cell free assays)
Formal name: N-[4-[[4-(1-methylethyl)-1-piperazinyl]sulfonyl]phenyl]-2-nitro-4-(trifluoromethyl)-benzamide, monohydrochloride
Synonyms:
Molecular weight: 537
CAS: 2109450-40-8
Purity: ≥98%
Formulation: A solid