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HCV

HCV (hepatitis C virus ) is a enveloped single-stranded RNA virus of the Flavivridae family. It lead to acute hepatitis, chronic liver disease and liver cancer.

Products for  HCV

  1. Cat.No. Product Name Information
  2. GC32344 Sofosbuvir impurity A Sofosbuvir impurity A, an diastereoisomer of Sofosbuvir, is the impurity of Sofosbuvir. Sofosbuvir impurity A  Chemical Structure
  3. GC34283 Sofosbuvir impurity B Sofosbuvir impurity B is an impurity of Sofosbuvir, Sofosbuvir is an active inhibitor of HCV RNA replication in the HCV replicon assay, demonstrates potent anti-hepatitis C virus (HCV) activity. Sofosbuvir impurity B  Chemical Structure
  4. GC30533 Sofosbuvir impurity C Sofosbuvir impurity C is an impurity of Sofosbuvir, Sofosbuvir is an active inhibitor of HCV RNA replication in the HCV replicon assay, demonstrates potent anti-hepatitis C virus (HCV) activity. Sofosbuvir impurity C  Chemical Structure
  5. GC34282 Sofosbuvir impurity D Sofosbuvir impurity D is an impurity of Sofosbuvir, Sofosbuvir is an active inhibitor of HCV RNA replication in the HCV replicon assay, demonstrates potent anti-hepatitis C virus (HCV) activity. Sofosbuvir impurity D  Chemical Structure
  6. GC34280 Sofosbuvir impurity E Sofosbuvir impurity E is an impurity of Sofosbuvir, Sofosbuvir is an active inhibitor of HCV RNA replication in the HCV replicon assay, demonstrates potent anti-hepatitis C virus (HCV) activity. Sofosbuvir impurity E  Chemical Structure
  7. GC30539 Sofosbuvir impurity F Sofosbuvir impurity F, an diastereoisomer of Sofosbuvir, is the impurity of Sofosbuvir. Sofosbuvir impurity F  Chemical Structure
  8. GC32339 Sofosbuvir impurity G Sofosbuvir impurity G, an diastereoisomer of Sofosbuvir, is the impurity of Sofosbuvir. Sofosbuvir impurity G  Chemical Structure
  9. GC34279 Sofosbuvir impurity H Sofosbuvir impurity H, an diastereoisomer of Sofosbuvir, is the impurity of Sofosbuvir. Sofosbuvir impurity H  Chemical Structure
  10. GC34284 Sofosbuvir impurity I Sofosbuvir impurity I, an diastereoisomer of Sofosbuvir, is the impurity of Sofosbuvir. Sofosbuvir impurity I  Chemical Structure
  11. GC32350 Sofosbuvir impurity J Sofosbuvir impurity J, an diastereoisomer of Sofosbuvir, is the impurity of Sofosbuvir. Sofosbuvir impurity J  Chemical Structure
  12. GC30522 Sofosbuvir impurity K Sofosbuvir impurity K, an diastereoisomer of Sofosbuvir, is the impurity of Sofosbuvir. Sofosbuvir impurity K  Chemical Structure
  13. GC34278 Sofosbuvir impurity L Sofosbuvir impurity L, an diastereoisomer of Sofosbuvir, is the impurity of Sofosbuvir. Sofosbuvir impurity L  Chemical Structure
  14. GC30524 Sofosbuvir impurity M Sofosbuvir impurity M, an diastereoisomer of Sofosbuvir, is the impurity of Sofosbuvir. Sofosbuvir impurity M  Chemical Structure
  15. GC30563 Sofosbuvir impurity N Sofosbuvir impurity N, an diastereoisomer of Sofosbuvir, is the impurity of Sofosbuvir. Sofosbuvir impurity N  Chemical Structure
  16. GC12350 T 705 T 705 (T-705) is a potent viral RNA polymerase inhibitor, it is phosphoribosylated by cellular enzymes to its active form, T 705-ribofuranosyl-5′-triphosphate (RTP). T 705  Chemical Structure
  17. GC37740 Taribavirin Taribavirin is an orally active inosine monophosphate dehydrogenase inhibitor, has activity against a wide range of viruses, especially the hepatitis C virus and influenza virus. Taribavirin  Chemical Structure
  18. GC38559 Taribavirin hydrochloride Taribavirin hydrochloride is an orally active inosine monophosphate dehydrogenase inhibitor, has activity against a wide range of viruses, especially the hepatitis C virus and influenza virus. Taribavirin hydrochloride  Chemical Structure
  19. GC16887 Tegobuvir A non-nucleoside inhibitor of HCV NS5B Tegobuvir  Chemical Structure
  20. GC12299 Telaprevir (VX-950) An HCV NS3/4A protease inhibitor Telaprevir (VX-950)  Chemical Structure
  21. GC13699 TMC647055 inhibitor of the hepatitis C virus NS5B polymerase TMC647055  Chemical Structure
  22. GC37802 TMC647055 Choline salt TMC647055 (Choline salt) is a potent nonnucleoside NS5B polymerase inhibitor of HCV replication. TMC647055 Choline salt  Chemical Structure
  23. GC70051 Trachelogenin

    Trachelogenin ((-)-Trachelogenin) is an HCV entry inhibitor that is not genotype-specific and has low cytotoxicity. Trachelogenin inhibits HCVcc infection and HCVpp cell entry in a dose-dependent manner, with IC50 values of 0.325 and 0.259 μg/mL in the HCVcc and HCVpp models, respectively. Trachelogenin has antiviral, anti-inflammatory, and analgesic effects.

    Trachelogenin  Chemical Structure
  24. GC32392 Tris(4-aminophenyl)methane (Leucopararosaniline) Tris(4-aminophenyl)methane (Leucopararosaniline) is a triphenylmethane dye. Tris(4-aminophenyl)methane (Leucopararosaniline)  Chemical Structure
  25. GC61359 TTP-8307 TTP-8307 is a potent inhibitor of the replication of several rhino- and enteroviruses. TTP-8307  Chemical Structure
  26. GC63248 Valopicitabine Valopicitabine (NM283) is a nucleoside analog and the orally bioavailable prodrug of the potent anti-HCV agent 2'-C-methylcytidine (NM107). Valopicitabine  Chemical Structure
  27. GC63635 Valopicitabine dihydrochloride Valopicitabine (NM283) dihydrochloride is a nucleoside analog and the orally bioavailable prodrug of the potent anti-HCV agent 2'-C-methylcytidine (NM107). Valopicitabine dihydrochloride  Chemical Structure
  28. GC10155 Vaniprevir Vaniprevir  Chemical Structure
  29. GC11830 VCH-916 VCH-916  Chemical Structure
  30. GC19372 Velpatasvir Velpatasvir (VEL, GS-5816) is a novel pan-genotypic hepatitis C virus (HCV) nonstructural protein 5A (NS5A) inhibitor with activity against genotype 1 (GT1) to GT6 HCV replicons. Velpatasvir  Chemical Structure
  31. GC10832 VX-222 (VCH-222, Lomibuvir) An HCV polymerase inhibitor VX-222 (VCH-222, Lomibuvir)  Chemical Structure

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