Ni Zhi-Jie, Wagman Allan S
Chiron Corporation, 4560 Horton Street, Emeryville, CA 94608, USA.
Curr Opin Drug Discov Devel. 2004 Jul;7(4):446-59.
Hepatitis C virus (HCV) is a disease that has a growing impact worldwide. A combination therapy comprising interferon-alpha (IFNalpha) and ribavirin represents the current standard treatment for chronic HCV infection, although it has demonstrated limited success and causes some serious side effects. Promising alternative approaches toward the control of HCV infection, and the development of new antiviral agents, include the use of NS3/4A serine protease and NS5B polymerase inhibitors. Successful proof-of-concept clinical trials of the NS3/4A protease inhibitor BILN-2061 have confirmed the usefulness of a peptidomimetic product-based approach, providing impetus for the generation of improved molecules. Preclinical results from the development of HCV polymerase inhibitors, both nucleoside and non-nucleoside, are promising. This review provides an overview of recent progress in these areas, and discusses the potential of various approaches toward small molecule HCV antivirals.
丙型肝炎病毒(HCV)是一种在全球范围内影响日益增大的疾病。由α干扰素(IFNα)和利巴韦林组成的联合疗法是目前慢性HCV感染的标准治疗方法,不过其疗效有限且会引发一些严重的副作用。控制HCV感染的有前景的替代方法以及新型抗病毒药物的研发,包括使用NS3/4A丝氨酸蛋白酶和NS5B聚合酶抑制剂。NS3/4A蛋白酶抑制剂BILN - 2061的概念验证临床试验取得成功,证实了基于拟肽产品方法的有效性,为研发改良分子提供了动力。核苷类和非核苷类HCV聚合酶抑制剂的临床前研发结果很有前景。本综述概述了这些领域的最新进展,并讨论了各种小分子HCV抗病毒方法的潜力。