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Voxilaprevir
CAS No. : 1535212-07-7
Biological Activity：Voxilaprevir (GS-9857) is a noncovalent, reversible inhibitor of HCV NS3/4A protease inhibitor (PI) with pangenotypic antiviral activity. Voxilaprevir inhibits genotype 1b and 3a wild-type NS3 proteases with Ki values of 0.038 nM and 0.066 nM, respectively. Voxilaprevir is an orally active direct-acting antiviral agent (DAA) and can be used for HCV infection research[2].
Research Area：Infection
Targets：HCV Protease
Related Screening Libraries:Drug Repurposing Compound Library Plus;FDA-Approved Drug Library Plus;FDA-Approved Drug Library Mini;Bioactive Compound Library Plus;Anti-Infection Compound Library;Metabolism/Protease Compound Library;FDA-Approved Drug Library;Antiviral Compound Library;Drug Repurposing Compound Library;Orally Active Compound Library;FDA Approved & Pharmacopeial Drug Library;Anti-Hepatitis C Virus Compound Library;Targeted Diversity Library;Protein-protein Interaction Inhibitor Library;EMA-Approved Drug Library;
Related Small Molecules:NS5A-IN-1;Grazoprevir potassium salt;BMS-986144;Ciluprevir;Faldaprevir-d6;Isoeuphorbetin;NS5A-IN-4;Coblopasvir;Glecaprevir;NS5A-IN-3;HCVP-IN-1;Paritaprevir dihydrate;Clemizole hydrochloride;BI-1230;AZD-7295;Faldaprevir;IDX184;HZ-1157;GSK2818713;Narlaprevir;AL-611
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