New class of antitubercular compounds: synthesis and anti-tubercular activity of 4-substituted pyrrolo[2,3-c]quinolines

被引:36
作者
Akula, Mahesh [1 ]
Sridevi, Jonnalagadda Padma [2 ]
Yogeeswari, P. [2 ]
Sriram, D. [2 ]
Bhattacharya, Anupam [1 ]
机构
[1] Birla Inst Technol & Sci, Dept Chem, Hyderabad 500078, Andhra Pradesh, India
[2] Birla Inst Technol & Sci, Dept Pharm, Hyderabad 500078, Andhra Pradesh, India
来源
MONATSHEFTE FUR CHEMIE | 2014年 / 145卷 / 05期
关键词
Heterocycles; Strained molecules; Aldehydes; Mannich reaction; Antitubercular; PYRROLOQUINOLINE ALKALOIDS; BIOLOGICAL EVALUATION; IN-VITRO; MARINOQUINOLINES; DERIVATIVES; APLIDIOPSAMINE; ANALOGS;
D O I
10.1007/s00706-013-1141-1
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Modified synthesis and antitubercular activity of 4-substituted pyrrolo[2,3-c]quinolines are reported. Some of the compounds showed significant antitubercular activity, when compared to some of the existing antitubercular drugs. A compound with an imidazole moiety at position 4 shows the highest activity and least toxicity.
引用
收藏
页码:811 / 819
页数:9
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