Name | (2S,3S)-N-[[2-methoxy-5-[5-(trifluoromethyl)tetrazol-1-yl]phenyl]methyl]-2-phenylpiperidin-3-amine,dihydrochloride |
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Synonyms |
Vofopitant dihydrochloride (USAN)
Vofopitant hydrochloride Vofopitant HCl |
Description | Vofopitant dihydrochloride (GR 205171A) is a potent, selective and orally available tachykinin neurokinin 1(NK1) receptor antagonist, inhibits [3H]SP binding to the NK1 receptor with pKi values of 9.5 and 10.6 in rat and human membranes respectively, acts as a potential broad-spectrum anti-emetic agent[1]. |
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Related Catalog | |
Target |
pKi: 9.5 (NK1, rat), 10.6 (NK1, human)[1] |
References |
Boiling Point | 542.5ºC at 760mmHg |
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Molecular Formula | C21H25Cl2F3N6O |
Molecular Weight | 505.36400 |
Flash Point | 281.9ºC |
Exact Mass | 504.14200 |
PSA | 82.09000 |
LogP | 5.59630 |
Vapour Pressure | 7.83E-12mmHg at 25°C |