Privileged s-triazines: structure and pharmacological applications

被引:72
|
作者
Shah, Dhruvin R. [1 ]
Modh, Rahul P. [1 ]
Chikhalia, Kishor H. [1 ]
机构
[1] Gujarat Univ, Sch Sci, Dept Chem, Ahmadabad 380009, Gujarat, India
关键词
REVERSE-TRANSCRIPTASE INHIBITORS; ANTI-HIV EVALUATION; BIOLOGICAL EVALUATION; 2,4,6-TRISUBSTITUTED TRIAZINES; ANTIMICROBIAL ACTIVITY; ANTITUMOR-ACTIVITY; HIGHLY POTENT; DERIVATIVES; DISCOVERY; DESIGN;
D O I
10.4155/fmc.13.212
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
This review summarizes recent reports on s-triazine and its respective analogs from the medicinal chemistry angle. Due to its high reactivity and binding characteristic towards various enzymes, s-triazine has attracted attention. This is combined with facile synthesis and interesting pharmacology. The triazine class demonstrates wide biological applications - including antimicrobial, antituberculosis, anticancer, antiviral and antimalarial. In this article the library of s-triazine-based molecular designs has been collated with respective bioactivity. Compounds are further compared with other heterocyclic/nontriazine moieties to correlate the efficiency of privileged s-triazine. We hope this article may assist chemists in their drug design and discovery efforts.
引用
收藏
页码:463 / 477
页数:15
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