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HCV

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HCV

Chemical Structure Cat. No. Product Name CAS No.
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.
ML-336 Chemical Structure
BCP37985 ML-336 1613465-33-0
ML-336 is an inhibitor of of the Venezuelan equine encephalitis virus (VEEV) strain TC-83.
PSI-352938 Chemical Structure
BCP35662 PSI-352938 1231747-17-3
PSI-352938 is a HCV NS5B inhibitor potentially for the treatment of HCV infection.
IDX 320 Chemical Structure
BCP34858 IDX 320 1251165-81-7
IDX320 is a potent non-covalent macrocyclic inhibitor of the HCV NS3/4A protease.
Grazoprevir potassium Chemical Structure
BCP34806 Grazoprevir potassium 1206524-86-8
Grazoprevir potassium is a selective inhibitor of Hepatitis C virus NS3/4a protease with broad activity across genotypes and resistant variants, with Kis of 0.01 nM (gt1b), 0.01 nM (gt1a), 0.08 nM (gt2a), 0.15 nM (gt2b), 0.90 nM (gt3a), respectively.
INX 08189 Chemical Structure
BCP34230 INX 08189 1234490-83-5
INX 08189 is an RNA-directed RNA polymerase (NS5B) inhibitor potentially for the treatment of HCV infection.
Dasabuvir sodium monohydrate Chemical Structure
BCP25424 Dasabuvir sodium monohydrate 1456607-55-8
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