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Vaniprevir

Chemical Structure : Vaniprevir

CAS No.: 923590-37-8

Vaniprevir (MK-7009;MK7009;MK 7009)

Catalog No.: PC-42481Not For Human Use, Lab Use Only.

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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Purity & Documentation Purity: >98% (HPLC) Select Batch:

Biological Activity

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; displays excellent selectivity against both a range of human proteases and a broad panel of pharmacologically relevant targets; has replicon EC50 of 3 and 9 nM for GT1b and 2a, respectively, has good plasma exposure and excellent liver exposure in multiple species.

HCV Infection

Approved

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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