4 Results for "

HCV genotypes 6a

" in MedChemExpress (MCE) Product Catalog:
Products (4)

4 Results for "HCV genotypes 6a" in MCE Product Catalog:

9
9 Cited Publications
Cat. No.: HY-13997
CAS No.: 1258226-87-7
Purity:  98.59%
Synonyms: ABT-267
Target:  

HCV

Research Areas:  

Infection

Ombitasvir is a potent inhibitor of the hepatitis C virus protein NS5A, with EC50s of 0.82 to 19.3 pM against HCV genotypes 1 to 5, and 366 pM against genotype 6a.
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Cat. No.: HY-131905S
CAS No.: 1606150-08-6
BMS-986144 is an orally active inhibitor of HCV NS3/4A protease. BMS-986144 binds to the active site of HCV NS3/4A protease and induces conformational changes in the protease. BMS-986144 reduces time-dependent CYP3A4 inhibition, exhibits hepatic microsomal metabolic stability, and undergoes oxidation of the macrocyclic linker chain. BMS-986144 can be used in studies related to hepatitis C virus infection .
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Cat. No.: HY-13997R
CAS No.: 1258226-87-7
Synonyms: ABT-267 (Standard)
Target:  

HCV Reference Standards

Research Areas:  

Infection

Ombitasvir (Standard) is the analytical standard of Ombitasvir. This product is intended for research and analytical applications. Ombitasvir is a potent inhibitor of the hepatitis C virus protein NS5A, with EC50s of 0.82 to 19.3 pM against HCV genotypes 1 to 5, and 366 pM against genotype 6a.
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Cat. No.: HY-184880
CAS No.: 1410114-25-8
Target:  

HCV Protease HCV

Research Areas:  

Infection

BMS-986144 non-deuterated is the non-tritium form of BMS-986144 (HY-131905S). BMS-986144 non-deuterated is an orally active inhibitor of HCV NS3/4A protease. BMS-986144 non-deuterated binds to the active site of HCV NS3/4A protease and induces conformational changes in the protease. BMS-986144 non-deuterated reduces time-dependent CYP3A4 inhibition, exhibits hepatic microsomal metabolic stability, and undergoes oxidation of the macrocyclic linker chain. BMS-986144 non-deuterated can be used in studies related to hepatitis C virus infection .
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