4.6 Review

Virtual Screening in Hepatitis B Virus Drug Discovery: Current State-of-the-Art and Future Perspectives

期刊

CURRENT MEDICINAL CHEMISTRY
卷 25, 期 23, 页码 2709-2721

出版社

BENTHAM SCIENCE PUBL LTD
DOI: 10.2174/0929867325666180221141451

关键词

Ligand-based virtual screening; structure-based virtual screening; quantitative structure-activity relationships; docking; Hepatitis B Virus; inhibitors; workflow

向作者/读者索取更多资源

Hepatitis B Virus (HBV) is a major global health burden. Interferon alpha and nucleos(t)ide analogues are currently the standard-of-care for chronic HBV infection. However, these antiviral agents have limited efficacy and do not result in a sustained virological response in the majority of infected patients. Virtual Screening (VS) strategies have now a strong impact on drug discovery, the strength of this research field has been corroborated by recent contributions in the development of novel drug candidates which are in clinical trials or which are already available in the clinics. In this context, different VS strategies have been applied to HBV in order to discover novel inhibitors. In this review, we summarize the VS efforts to identify and design novel HBV interventions. We believe that the combination of in silico and in vitro tools can lead to faster validation of novel drug targets which could accelerate the HBV drug discovery and development efforts.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据