Chemical Structure : BMS-929075
Catalog No.: PC-60427Not For Human Use, Lab Use Only.
A highly potent, selective, orally bioavailable HCV NS5B polymerase inhibitor with IC50 of 9, 4, and 18 nM for GT1a, GT1b, and GT1b-C316N mutant in HCV replicon assay, respectively.
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A highly potent, selective, orally bioavailable HCV NS5B polymerase inhibitor with IC50 of 9, 4, and 18 nM for GT1a, GT1b, and GT1b-C316N mutant in HCV replicon assay, respectively; possesses excellent pharmacokinetic parameters across preclinical animal species.
HCV Infection
Phase 1 Clinical
M.Wt | 538.5548 | |
Formula | C31H24F2N4O3 | |
Appearance | Solid | |
Storage |
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Solubility |
10 mM in DMSO |
1. Yeung KS, et al. J Med Chem. 2017 May 25;60(10):4369-4385.
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