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Vaniprevir

Chemical Structure : Vaniprevir

CAS No.: 923590-37-8

Vaniprevir (MK-7009, MK7009)

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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Biological Activity

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.

Physicochemical Properties

M.Wt 757.9364
Formula C38H55N5O9S
Appearance Solid
CAS No.
Storage
Solide Powder
-20 °C 12 Months; 4°C 6 Months
In Solvent
-80 °C 6 Months; -20°C 6 Months
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

Cyclopropanecarboxamide, N-[[[6-(2-carboxy-2,3-dihydro-1H-isoindol-4-yl)-2,2-dimethylhexyl]oxy]carbonyl]-3-methyl-L-valyl-(4R)-4-hydroxy-L-prolyl-1-amino-N-(cyclopropylsulfonyl)-2-ethyl-, (12)-lactone, (1R,2R)-

References

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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