Synthesis, antimicrobial, and anti-inflammatory activities of acetamido pyrrolyl azoles

被引:0
作者
Donthamsetty V. Sowmya
Shaik Sharafuddin Basha
Palampalli Uma Maheswari Devi
Yerraguravagari Lavanyalatha
Adivireddy Padmaja
Venkatapuram Padmavathi
机构
[1] Sri Venkateswara University,
[2] Sri Padmavathi Mahilavisvavidyalayam,undefined
来源
Medicinal Chemistry Research | 2017年 / 26卷
关键词
Pyrrole; Oxazole; Thiazole; Imidazole; Antimicrobial activity; Anti-inflammatory activity;
D O I
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中图分类号
学科分类号
摘要
The acetamido pyrrolyl oxazoles/thiazoles/imidazoles were prepared and tested for their antimicrobial and anti-inflammatory activities. The nitro substituted acetamido pyrrolyl thiazole (11f) and pyrrolyl imidazole (12f) exhibited promising antibacterial activity against K. pneumoniae. The compound 12f showed good antifungal activity against P. chrysogenum. The methoxy acetamido pyrrolyl oxazole (10c) displayed potential anti-inflammatory activity.
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页码:1010 / 1021
页数:11
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共 150 条
[1]  
Amarnath Reddy L(2010)Synthesis and process optimization of amtolmetin: an antiinflammatory agent Org Process Res Dev 14 362-368
[2]  
Chakraborty S(2002)Antibacterial activity of crude aqeous extracts of World J Biotechnol 3 347-357
[3]  
Swapna R(2015) on J Med Chem Res 24 954-964
[4]  
Dinesh B(1995)Synthesis and antimicrobial activity of 3-aroyl-4-heteroaryl pyrroles and pyrazoles J Med Chem 38 4929-4936
[5]  
China Malakondaiah G(2014)Phenethylthiazolethiourea (PETT) compounds, a new class of HIV- 1 reverse transcriptase inhibitors. 1. Synthesis and basic structure-activity relationship studies of PETT analogs Eur J Med Chem 82 347-354
[6]  
Ravikumar M(2013)Synthesis and antimicrobial activity of amine linked bis- and tris-heterocycles Chem Pharm Bull 61 516-523
[7]  
Kumar A(2009)Synthesis and antimicrobial activity of azole derivatives J Sci Eng Technol 5 143-150
[8]  
Srinivas Reddy G(1999)Antibacterial property of different medicinal plants: J Am Chem Soc 121 54-62
[9]  
Jyothirmayi N(1999), J Med Chem 42 5064-5071
[10]  
Dwivedi N(1990), J Appl Bacteriol 69 498-503