Isatin hybrids and their anti-tuberculosis activity

被引:237
作者
Xu, Zhi [1 ]
Zhang, Shu [2 ]
Gao, Chuan [3 ]
Fan, Jing [4 ]
Zhao, Feng [3 ]
Lv, Zao-Sheng [1 ]
Feng, Lian-Shun [1 ,3 ,5 ]
机构
[1] Wuhan Univ Sci & Technol, Wuhan 430081, Peoples R China
[2] Pony Testing Int Grp, Wuhan 430034, Peoples R China
[3] WuXi AppTec, Wuhan 430075, Peoples R China
[4] Hengshui Univ, Hengshui 053000, Peoples R China
[5] Peking Univ, Synthet & Funct Biomol Ctr, Beijing 100871, Peoples R China
关键词
Isatin hybrids; Mycobacterium tuberculosis; Quinolone; Structure-activity relationship; Review; VITRO ANTIMYCOBACTERIAL ACTIVITY; MYCOBACTERIUM-TUBERCULOSIS; MOLECULAR HYBRIDIZATION; MANNICH-BASES; ANTI-HIV; DERIVATIVES; DESIGN; ANALOGS; ANTIBACTERIAL; ANTIMALARIAL;
D O I
10.1016/j.cclet.2016.07.032
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Tuberculosis (TB) is one of the most common and even fatal infectious diseases known to mankind. Millions of new cases are reported every year over the world, and one-third of the world's population is potentially infected with mycobacteria tuberculosis (MTB). Research to develop novel anti-TB drugs led to the identification of several isatin-based antimycobacterial agents, among which a number of potential candidates displayed excellent antimycobacterial activity and were found to be free of cytotoxicity. This review outlines the advances in the application of isatin hybrids as antimycobacterial agents and the critical aspects of design and structure-activity relationship of these derivatives. (C) 2016 Chinese Chemical Society and Institute of Materia Medica, Chinese Academy of Medical Sciences.
引用
收藏
页码:159 / 167
页数:9
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