Synthetic bicyclic iminosugar derivatives fused thiazolidin-4-one as new potential HIV-RT inhibitors

被引:18
|
作者
Chen, Hua [1 ]
Yang, Tianyu [1 ]
Wei, Sinan [1 ]
Zhang, Hongzhi [1 ]
Li, Rui [1 ]
Qin, Zhanbin [1 ]
Li, Xiaoliu [1 ]
机构
[1] Hebei Univ, Coll Chem & Environm Sci, Key Lab Chem Biol Hebei Prov, Baoding 071002, Peoples R China
基金
中国国家自然科学基金;
关键词
Bicyclic azasugar; Thiazolidin-4-one; HIV-RT inhibitor; Pummerer rearrangement; PUMMERER REACTION; INDOLIZIDINES;
D O I
10.1016/j.bmcl.2012.09.100
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Novel bicyclic iminosugar derivatives fused thiazolidin-4-one were conveniently synthesized by double Pummerer rearrangements, and their HIV reverse transcriptase (RT) inhibitory activities were preliminary examined. The notable anti-HIV-RT activity demonstrated that such bicyclic azasugars hold potential as a new kind of HIV-RT inhibitors. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:7041 / 7044
页数:4
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