4-Phenoxybenzylamine inhibits the function of the NS3 protein by stabilizing an inactive conformation with an IC50 of about 500 μM against FL NS3/4a.
IC50&Target
IC50: 500 μM (FL NS3/4a)
体外研究
A highly conserved novel binding site located at the interface between the protease and helicase domains of the Hepatitis C Virus (HCV) NS3 protein is identified. 4-Phenoxybenzylamine binding at this allosteric site inhibits the function of the NS3 protein by stabilizing an inactive conformation and thus represents a new class of direct acting antiviral agents.
分子式
C13H13NO
分子量
199.25
CAS号
107622-80-0
运输条件
Room temperature in continental US; may vary elsewhere.