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HCV

Chemical Structure Cat. No. Product Name CAS No.
Voxilaprevir Chemical Structure
 BCP24118 Voxilaprevir 1535212-07-7
Voxilaprevir (GS-9857) is a potent HCV NS3/4A protease inhibitor that is used in combination with sofosbuvir and velpatasvir for treatment of HCV infection.
Ciluprevir Chemical Structure
 BCP24756 Ciluprevir 300832-84-2
Ciluprevir is an orally bioavailable, peptidomimetic, macrocyclic compound with activity against hepatitis C virus (HCV). Ciluprevir binds non-covalently to the active center of the HCV NS3-4A serine protease and prevents processing of viral proteins required for replication.
2'-Deoxy-2'-fluoro-5-iodocytidine Chemical Structure
 BCP47775 2'-Deoxy-2'-fluoro-5-iodocytidine 80791-93-1
2'-Deoxy-2'-fluoro-5-iodocytidine is a potent anti-​hepatitis C virus (HCV) agent.
Ruzasvir Chemical Structure
 BCP47999 Ruzasvir 1613081-64-3
Ruzasvir is a pan-genotypic HCV nonstructural protein 5A (NS5A) inhibitor with a "flat" GT1 mutant profile.
Myriocin Chemical Structure
 BCP46480 Myriocin 35891-70-4
Myriocin is an unsaturated hydrocarbon and fatty acid derivative produced by Myriococcum albomyces NRRL 3858. It has antifungal activity.
RO-9187 Chemical Structure
 BCP46487 RO-9187 876708-03-1
RO-9187 is a potent inhibitor of HCV virus replication with an IC50 of 171 nM.
AT-527 Chemical Structure
 BCP42710 AT-527 2241337-84-6
AT-527, a hemisulfate salt of AT-511, a guanosine nucleotide prodrug, is a potent and orally active HCV viral replication inhibitor.
MK 8876 Chemical Structure
 BCP42768 MK 8876 1426960-33-9
MK-8876 is a HCV NS5B Site D Inhibitor.
U 18666A Chemical Structure
 BCP41254 U 18666A 3039-71-2
U 18666A is a cell-permeable and amphiphilic amino-steroid that inhibits cholesterol synthesis and cellular transport via the suppression of 2,3-oxidosqualene-lanosterol cyclase activity. U 18666A also acts as a weak inhibitor of hedgehog (Hh) signaling. It has been shown to reduce serum sterol levels in rats in vivo.
R-1479 Chemical Structure
 BCP38817 R-1479 478182-28-4
R1479 is a potent and highly specific inhibitor of HCV replication in cell culture, and that its triphosphate is a potent and highly selective inhibitor of NS5B mediated RNA synthesis, the HCV encoded RNA polymerase.
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