Antiviral activity and resistance of HCV NS5A replication complex inhibitors

被引:115
作者
Gao, Min [1 ]
机构
[1] Bristol Myers Squibb Co, Wallingford, CT 06492 USA
关键词
HEPATITIS-C-VIRUS; NONSTRUCTURAL PROTEIN 5A; RNA REPLICATION; IN-VITRO; BMS-790052; PHOSPHORYLATION; DOMAIN; IDENTIFICATION; VARIANTS; MODES;
D O I
10.1016/j.coviro.2013.06.014
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Treatment of Hepatitis C Virus (HCV) infection is rapidly evolving with the introduction of direct acting antiviral agents (DAA). HCV NS5A replication complex inhibitors, exemplified by Daclatasvir (BMS-790052), represent a new class of DAA. The exceptional in vitro potency (EC50 values at pM to low nM range) and broad genotype coverage of NS5A inhibitors have translated to robust anti-HCV effects in infected patients, making NS5A inhibitors an essential component of effective HCV DAA combination therapies. On the basis of drug-induced resistance substitutions and computer modeling, NS5A inhibitors most likely act at the N-terminus of NS5A (domain l). Mechanism of inhibition studies to elucidate the exquisite potency of these inhibitors have generated several working models.
引用
收藏
页码:514 / 520
页数:7
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