Home   >  
Microbiology/Virology
  >  
HCV

Classified by application

All Products

Signaling Pathways

Research Areas

Nature products

Antibodies

Peptides

Catalysts

Impurities

Intermediate

Raw Materials

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.
123下一页末页共 67 条记录 1 / 7 页 
0086-13720134139