NS3 and its cofactor NS4A make up the complex known as HCV NS3-4A serine protease. It is crucial for processing viral polyproteins, RNA replication, and virion formation and contains serine protease and NTPase/RNA helicase activities.
The HCV NS3/4A protease efficiently cleaves and inactivates two important signaling molecules in the sensory pathways that react to HCV pathogen-associated molecular patterns (PAMPs) to induce interferons (IFNs), i.e., mitochondrial antiviral signaling protein (MAVS) and Toll-IL-1 receptor domain-containing adaptor inducing IFN-β (TRIF). HCV infection is associated with chronic liver disease, including hepatic steatosis, fibrosis, cirrhosis, and hepatocellular carcinoma. The NS3-4A serine protease of HCV has been one of the most attractive targets for developing specific antiviral agents against HCV.
| Structure | Cat No. | Product Name | CAS No. | Product Description |
|---|---|---|---|---|
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V22361 | HZ-1157 | 1009734-33-1 | HZ-1157 can inhibit HCV (hepatitis C virus) NS3/4A protease with IC50 of 1.0 μmol/L. |
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V98443 | Ac-DEMEEC-OH | 208921-05-5 | Ac-DEMEEC-OH is a competitive inhibitor of HCV NS3 protease (Ki: 0.6 µM). |
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V115985 | AV-4025 hydrochloride | 1380290-35-6 | AV-4025 hydrochloride (compound 13a) is an orally effective NS5A inhibitor. |
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V116295 | BMS 605339 | 630417-82-2 | BMS 605339 is a linear tetrapeptide α-ketoamide HCV NS3 protease inhibitor. |
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V94268 | Faldaprevir sodium | 1215856-44-2 | Fadapvir sodium is an orally active, selective, non-covalent inhibitor of the NS3/4A protease of hepatitis C virus (HCV) genotypes 1a and 1b with Ki values of 2.6 and 2.0 nM, respectively. |
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V112019 | Furaprevir | 1435923-88-8 | Furapuvir is a potent and selective HCV NS3/4A protease inhibitor. |
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V117955 | HCV-IN-50 | 303776-85-4 | HCV-IN-50 (compound 2) is a competitive and selective HCV NS5B RNA-dependent RNA polymerase inhibitor. |
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V116050 | IDX-320 | 1251165-81-7 | IDX-320 is a derivative of piperidine acid. |
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V116300 | MK 6325 | 1263814-52-3 | MK 6325 is an HCV NS3/4a protease inhibitor. |
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V115731 | MK-2748 | 1193902-95-2 | MK-2748 is a hepatitis C virus (HCV) NS3/4a protease inhibitor. |
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V80973 | NS5A-IN-1 | NS5A-IN-1 is a precursor of the hepatitis C virus NS5A inhibitor Pibrentasvir (ABT-530). | |
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V73168 | NS5A-IN-2 | 2764786-74-3 | NS5A-IN-2 (Compound 33) is a potent NS5A inhibitor. |
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V73169 | NS5A-IN-3 | 2764786-56-1 | NS5A-IN-3 (Compound 15) is a potent NS5A inhibitor. |
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V3915 | VOXILAPREVIR | 1535212-07-7 | Voxilaprevir (formerly GS-9857; GS9857;trade name:Vosevi) is a hepatitis C virus nonstructural protein (HCV NS) 3/4A protease inhibitor developed by Gilead and approved in 2017 as an anti-HCV drug for use in combination with sofosbuvir and velpatasvir. |
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V3159 | Grazoprevir | 1350514-68-9 | Grazoprevir (formerly MK-5172;MK5172; trade name: Zepatier) is a 2nd generation and selective inhibitor of theHepatitis C Virus NS3/4A Proteaseapproved by FDA in 2016 for the treatment of hepatitis C (used in combination with elbasvir, an NS5A replication complex inhibitor). |
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V9749 | Faldaprevir | 801283-95-4 | Faldaprevir (BI201335; BI-201335) is a novel and potent potent NS3/NS4A protease inhibitor with the potential to be used inthe treatment of HCV infection. |
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V3157 | Boceprevir (EBP-520; SCH-503034) | 394730-60-0 | Boceprevir (previously known as EBP 520; SCH 503034; trade name: Victrelis) is a novel, orally bioavailable, selective, direct acting inhibitor ofhepatitis C virus (HCV) protease with Ki value of 14 nM for NS3 in an enzyme assay andEC90of 350 nM in cell-based replicon assay. |
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