Triazole derivatives and their anti-tubercular activity

被引:421
|
作者
Zhang, Shu [1 ,2 ]
Xu, Zhi [2 ]
Gao, Chuan [3 ]
Ren, Qing-Cheng [3 ]
Chang, Le [3 ]
Lv, Zao-Sheng [2 ]
Feng, Lian-Shun [3 ]
机构
[1] Pony Testing Int Grp Wuhan, Wuhan, Hubei, Peoples R China
[2] Wuhan Univ Sci & Technol, Key Lab Hubei Prov Coal Convers & New Carbon Mat, Wuhan, Hubei, Peoples R China
[3] WuXi AppTec Wuhan, Wuhan, Hubei, Peoples R China
关键词
Triazole; Hybrid compounds; Anti-tuberculosis activity; Anti-mycobacterial activity; Structure-activity relationship; FERROCENYLCHALCONE CONJUGATES SYNTHESIS; LINKED COUMARINYL TRIAZOLES; CLICK CHEMISTRY APPROACH; BETA-LACTAM-FERROCENE; IN-VITRO; ANTIMYCOBACTERIAL ACTIVITY; BIOLOGICAL EVALUATION; ANTITUBERCULAR EVALUATION; 1,2,3-TRIAZOLE DERIVATIVES; POTENT INHIBITORS;
D O I
10.1016/j.ejmech.2017.06.051
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Tuberculosis (TB) remains one of the most widespread and leading deadliest diseases, threats one-third of the world's population. Although numerous efforts have been undertaken to develop new anti-TB agents, only a handful of compounds have entered human trials in the past 5 decades. Triazoles including 1,2,3-triazole and 1,2,4-triazole are one of the most important classes of nitrogen containing heterocycles that exhibited various biological activities. Triazole derivatives are regarded as a new class of effective anti-TB candidates owing to their potential anti-TB potency. Thus, molecules containing triazole moiety may show promising in vitro and in vivo anti-TB activities and might be able to prevent the drug resistant to certain extent. This review outlines the advances in the application of triazole-containing hybrids as anti-TB agents, and discusses the structure-activity relationship of these derivatives. (C) 2017 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:501 / 513
页数:13
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