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HCV

Chemical Structure Cat. No. Product Name CAS No.
Boceprevir D9 Chemical Structure
BCP21353 Boceprevir D9 1256751-11-7
ITX-5061 HCl Chemical Structure
BCP30784 ITX-5061 HCl 1252679-52-9
ITX5061 is a type II inhibitor of p38 MAPK and also an antagonist of scavenger receptor B1 (SR-B1).
Uprifosbuvir Chemical Structure
BCP30560 Uprifosbuvir 1496551-77-9
Uprifosbuvir, also known as MK-3682 and IDX-21437, is an uridine nucleotide analog HCV NS5B polymerase inhibitor.
Pibrentasvir Chemical Structure
BCP24811 Pibrentasvir 1353900-92-1
Pibrentasvir, also known as ABT-530, is a protease inhibitor potentially for the treatment of HCV infection.
Beclabuvir Chemical Structure
BCP11013 Beclabuvir 958002-33-0
Beclabuvir is an allosteric inhibitor that binds to thumb site 1 of the hepatitis C virus (HCV) NS5B RNA-dependent RNA polymerase, and inhibits recombinant NS5B proteins from HCV genotypes 1, 3, 4, and 5 with IC50 of < 28 nM.
MK-4882 Chemical Structure
BCP13058 MK-4882 1246472-08-1
MK-4882 is a potent HCV NS5A inhibitor.
Elbasvir Chemical Structure
BCP29961 Elbasvir 1370468-36-2
Elbasvir (MK-8742) is a hepatitis C virus nonstructural protein 5A (HCV NS5A) inhibitor with EC50s of 4, 3 and 3 nM against genotype 1a, 1b, and 2a, respectively.
GS-566500 Chemical Structure
BCP28539 GS-566500 1233335-78-8
GS-566500 is a Sofosbuvir metabolite.
Sofosbuvir impurity K Chemical Structure
BCP24186 Sofosbuvir impurity K 1496552-51-2
Sofosbuvir impurity K, an diastereoisomer of sofosbuvir, is the impurity of sofosbuvir.
Sofosbuvir impurity G Chemical Structure
BCP16918 Sofosbuvir impurity G 1337482-15-1
Sofosbuvir impurity G, an diastereoisomer of sofosbuvir, is the impurity of sofosbuvir.
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