Synthesis and antimicrobial activity of 1H,10H-benzo[e]pyrrolo[3,2-g]indole derivatives

被引:0
|
作者
Sh. A. Samsoniya
M. V. Trapaidze
N. A. Kuprashvili
机构
[1] Ivane Javakhishvili Tbilisi State University,
来源
Pharmaceutical Chemistry Journal | 2009年 / 43卷
关键词
benzopyrroloindole; phenylazoderivatives; azocoupling; antimicrobial; antifungal; antituberculosis activity;
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中图分类号
学科分类号
摘要
We have synthesized a series of new phenylazo derivatives of 1H,10H-benzo[e]pyrrolo[3, 2-g]indole containing 3-(p-bromophenylazo) (II), 3-(p-iodophenylazo) (III), 3-(p-sulfamidophenylazo) (IV), 3-formyl (V), 3,8-diformyl (VI), 3-phenylazo (VII), 3-(p-chlorophenylazo) (VIII), 3-(p-nitrophenylazo) (IX), 2,9-di(adamantylaminocarbonyl) (X), 2,9-di(p-benzenesulfamidoaminocarbonyl) (XI), 2,9-di(isonicotinoylhydrazidecarbonyl) (XII), and 2,9-di(carbohydrazide) (XIII) substituents. The antimicrobial, antifungal, and antituberculosis activity was investigated in vitro with respect to various microorganisms including conditionally pathogenic mycobacteria and pathogenic fungi. It is established that the tested compounds possess high antimicrobial activity. The synthesized compounds are of great interest for further, more thorough investigations and experiments on animals with the corresponding infectious diseases.
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页码:92 / 94
页数:2
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