Faldaprevir (BI 201335) is a potent, orally active and selective noncovalent inhibitor of NS3/4A protease of HCV (hepatitis C virus) genotypes 1a and 1b, with Ki values of 2.6 and 2.0 nM, respectively. Faldaprevir inhibits HCV RNA replication, with EC50 values of 6.5 and 3.1 nM, respectively. Faldaprevir has potent antiviral activity against chronic HCV infection[1][2].
Molecular Weight:
869.82
Purity:
98.58
CAS Number:
[801283-95-4]
Formula:
C40H49BrN6O9S
Target:
HCV Protease
Application Notes:
MCE Product type: Reference compound
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