Chemical Structure : Vaniprevir
Catalog No.: PC-42481Not For Human Use, Lab Use Only.
Vaniprevir (MK-7009) is a potent, selective, orally available inhibitor of HCV NS3/4A protease with Ki of 0.05 and 0.9 nM for GT1b and 2a protease, respectively.
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Vaniprevir (MK-7009) is a potent, selective, orally available inhibitor of HCV NS3/4A protease with Ki of 0.05 and 0.9 nM for GT1b and 2a protease, respectively.
Vaniprevir (MK-7009) displays excellent selectivity against both a range of human proteases and a broad panel of pharmacologically relevant targets.
Vaniprevir (MK-7009) has replicon EC50 of 3 and 9 nM for GT1b and 2a, respectively, has good plasma exposure and excellent liver exposure in multiple species.
M.Wt | 757.9364 | |
Formula | C38H55N5O9S | |
Appearance | Solid | |
Storage |
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Solubility |
10 mM in DMSO |
1. McCauley JA, et al. J Med Chem. 2010 Mar 25;53(6):2443-63.
2. Liverton NJ, et al. Antimicrob Agents Chemother. 2010 Jan;54(1):305-11.
3. Manns MP, et al. Hepatology. 2012 Sep;56(3):884-93.
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