4.7 Article

Characterization of 8-hydroxyquinoline derivatives containing aminobenzothiazole as inhibitors of dengue virus type 2 protease in vitro

期刊

ANTIVIRAL RESEARCH
卷 97, 期 1, 页码 74-80

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.antiviral.2012.10.009

关键词

Dengue virus protease inhibitors; Molecular modeling; Molegro virtual docker; Kinetic analysis; Competitive mode of inhibition; Sub-micromolar IC50

资金

  1. National Institutes of Health [AI070791-03S1, U01-AI082068]
  2. Biomedical Graduate Research Organization of Georgetown University
  3. NIH [U54 AI057159]

向作者/读者索取更多资源

Four serotypes of dengue virus (DENV1-4), mosquito-borne members of Flaviviridae family cause frequent epidemics causing considerable morbidity and mortality in humans throughout tropical regions of the world. There is no vaccine or antiviral therapeutics available for human use. In a previous study, we reported that compounds containing the 8-hydroxyquinoline (8-HQ) scaffold as inhibitors of West Nile virus serine protease. In this study, we analyzed potencies of some compounds with (8-HQ)-aminobenzothiazole derivatives for inhibition of DENV2 protease in vitro. We identified analogs 1-4 with 2-aminothiazole or 2-aminobenzothiazole scaffold with sub-micromolar potencies (IC50) in the in vitro protease assays. The kinetic constant (K-i) for the most potent 8-HQ-aminobenzothiazole inhibitor (compound 1) with an IC50 value of 0.91 +/- 0.05 mu M was determined to be 2.36 +/- 0.13 mu M. This compound inhibits the DENV2 NS2B/NS3pro by a competitive mode of inhibition. (C) 2012 Elsevier B.V. All rights reserved.

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

4.7
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