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Voxilaprevir is a pan-genotypic hepatitis C virus (HCV) non-structural 3/4A (NS3/4A) serine protease inhibitor. It inhibits replication of wild-type HCV genotypes 1a, 1b, 2a, 2b, 3a, 4a, 5a, and 6a (EC50s = 1.9-6.6 nM in replicon assays). Voxilaprevir also inhibits replication of mutant HCV genotypes containing NS3 resistance-associated substitutions (EC50s = 3.1, 2.7, and 4 nM for HCV genotypes 1a Q80K, 1a R155K, and 1b D168E, respectively). Formulations containing Voxilaprevir have been used in the treatment of chronic HCV infection.
Brand: BCM
Target: Hepatitis C virus (HCV) nonstructural protein (NS) 3/4A protease
pKa: 4.46±0.40(Predicted)
Solubility: Soluble in DMSO. Insolublei n Water.
InChi Key: MZBLZLWXUBZHSL-FZNJKFJKSA-N
Attribute [Chem Name] (33R,34S,35S,91R,92R,5S)-5-(tert-butyl)-N-((1R,2R)-2-(difluoromethyl)-1-(((1-methylcyclopropyl)sulfonyl)carbamoyl)cyclopropyl)-34-ethyl-14,14-difluoro-17-methoxy-4,7-dioxo-2,8-dioxa-6-aza-1(2,3)-quinoxalina-3(3,1)-pyrrolidina-9(1,2)-cyclopropanacyclotetradecaphane-35-carboxamide [Synonym] Voxilaprevir; GS-9857; GS 9857; GS9857; Vosevi [CAS No.] 1535212-07-7 [MDL No.] MFCD32174311 [Formula] C40H52F4N6O9S [Molecular] 868.93 [Form] White solid
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