亚基因组mRNA
化学
复制子
丝氨酸蛋白酶
丙型肝炎病毒
核糖核酸
病毒学
NS2-3蛋白酶
NS3型
蛋白酶抑制剂(药理学)
丝氨酸
干扰素
酶
分子生物学
蛋白酶
病毒
生物化学
生物
基因
基因组
病毒载量
抗逆转录病毒疗法
作者
Stéphane Bogen,Ashok Arasappan,Frank Bennett,Kevin Chen,Edwin Jao,Yi‐Tsung Liu,Raymond G. Lovey,Srikanth Venkatraman,Weidong Pan,Tajel Parekh,Russel Pike,Sumei Ruan,Rong Liu,Bahige M. Baroudy,Sony Agrawal,Robert A. Chase,Paul Ingravallo,John Pichardo,Andrew Prongay,Jean‐Marc Brisson
摘要
Introduction of various modified prolines at P(2) and optimization of the P(1) side chain led to the discovery of SCH6 (24, Table 2), a potent ketoamide inhibitor of the HCV NS3 serine protease. In addition to excellent enzyme potency (K(i)*= 3.8 nM), 24 was also found to be a potent inhibitor of HCV subgenomic RNA replication with IC(50) and IC(90) of 40 and 100 nM, respectively. Recently, antiviral activity of 24 was demonstrated with inhibition of the full-length genotype 2a HCV genome. In addition, 24 was found to restore the responsiveness of the interferon regulatory factor 3 (IRF-3) in cells containing HCV RNA replicons.
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