4-Phenoxybenzylamine inhibits the function of the NS3 protein by stabilizing an inactive conformation with an IC 50 of about 500 μM against FL NS3/4a.
性状
Liquid
IC50 & Target[1][2]
IC50: 500 μM (FL NS3/4a)
体外研究(In Vitro)
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. has not independently confirmed the accuracy of these methods. They are for reference only.
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
4°C, protect from light In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)
参考文献
[1]. Saalau-Bethell SM, et al. Discovery of an allosteric mechanism for the regulation of HCV NS3 protein function. Nat Chem Biol. 2012 Nov;8(11):920-5.
溶解度数据
In Vitro: DMSO : 12.5 mg/mL (62.74 mM; Need ultrasonic)配制储备液