Recent advances in 1,2,3-and 1,2,4-triazole hybrids as antimicrobials and their SAR: A critical review

被引:38
|
作者
Tian, Guimiao [1 ]
Song, Qiuyi [1 ]
Liu, Ziwei [1 ]
Guo, Ju [1 ]
Cao, Shuang [1 ]
Long, Sihui [1 ]
机构
[1] Wuhan Inst Technol, Hubei Engn Res Ctr Adv Fine Chem, Hubei Key Lab Novel Reactor & Green Chem Technol, Key Lab Green Chem Proc,Minist Educ,Sch Chem Engn, 206 Ist Rd Opt Valley, Wuhan 430205, Hubei, Peoples R China
关键词
Triazole; Derivatives; Antibacterial; Antifungal; SAR; TRIAZOLE DERIVATIVES; ANTIINFLAMMATORY ACTIVITY; MOLECULAR DOCKING; CLICK CHEMISTRY; DESIGN; ANTIBACTERIAL; ANTICANCER; ANTIOXIDANT;
D O I
10.1016/j.ejmech.2023.115603
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
With the widespread use and sometimes even abuse of antibiotics, the problem of bacterial resistance to anti-biotics has become very serious, and it is posing a great threat to global health. Therefore, development of new antibiotics is imperative. Triazoles are five-membered, nitrogen-containing aromatic heterocyclic scaffolds, with two isomeric forms, i.e. 1,2,3-triazole and 1,2,4-triazole. Triazole-containing compounds have a wide range of biological activities such as antibacterial, antifungal, anticancer, antioxidant, antitubercular, antimalarial, anti -HIV, anticonvulsant, anti-inflammatory, antiulcer, analgesic, and etc. The bioactivities and the diversity of triazole-containing drugs have attracted wide interest in these heterocycles. Various antibiotic triazole hybrids have been developed, and most of which have shown potent antimicrobial activities. In this review, we sum-marized the recent advances in triazole hybrids as potential antibacterial agents and their structure-activity relationships (SARs). The information gained through SAR studies will provide further insights into the devel-opment of new triazole antimicrobials.
引用
收藏
页数:25
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