Synthesis and biological evaluation of 1-(5-(2-chloroquinolin-3-yl)-3-phenyl-1H-pyrazol-1-yl)ethanone derivatives as potential antimicrobial agents

A novel series of 2-Chloroquinoline nucleus clubbed with the pyrazole ring has been synthesized and screened for antibacterial and antifungal activity. The results obtained were promising against both bacterial and fungal strains.   Among the series, compound MB-N was found moderately active against...

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Main Authors: Pankaj B. Miniyar, Mahesh A. Barmade, Anand A. Mahajan
Format: Article
Language:English
Published: Elsevier 2015-11-01
Series:Journal of Saudi Chemical Society
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S1319610313001348
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spelling doaj-dd15c85d734e499585aedc52032027a02020-11-25T01:57:23ZengElsevierJournal of Saudi Chemical Society1319-61032015-11-0119665566010.1016/j.jscs.2013.12.004Synthesis and biological evaluation of 1-(5-(2-chloroquinolin-3-yl)-3-phenyl-1H-pyrazol-1-yl)ethanone derivatives as potential antimicrobial agentsPankaj B. MiniyarMahesh A. BarmadeAnand A. MahajanA novel series of 2-Chloroquinoline nucleus clubbed with the pyrazole ring has been synthesized and screened for antibacterial and antifungal activity. The results obtained were promising against both bacterial and fungal strains.   Among the series, compound MB-N was found moderately active against Aspergillus fumigatus, Penicillium notatum and Bacillus subtilis having MIC 48, 46 and 44 μg/ml, respectively whereas compound MB-A was found active against P. notatum, B. subtilis and Escherichia coli having MIC 57, 54 and 43 μg/ml, respectively as compared to standard.http://www.sciencedirect.com/science/article/pii/S1319610313001348QuinolinePyrazoleAntibacterialAntifungal
collection DOAJ
language English
format Article
sources DOAJ
author Pankaj B. Miniyar
Mahesh A. Barmade
Anand A. Mahajan
spellingShingle Pankaj B. Miniyar
Mahesh A. Barmade
Anand A. Mahajan
Synthesis and biological evaluation of 1-(5-(2-chloroquinolin-3-yl)-3-phenyl-1H-pyrazol-1-yl)ethanone derivatives as potential antimicrobial agents
Journal of Saudi Chemical Society
Quinoline
Pyrazole
Antibacterial
Antifungal
author_facet Pankaj B. Miniyar
Mahesh A. Barmade
Anand A. Mahajan
author_sort Pankaj B. Miniyar
title Synthesis and biological evaluation of 1-(5-(2-chloroquinolin-3-yl)-3-phenyl-1H-pyrazol-1-yl)ethanone derivatives as potential antimicrobial agents
title_short Synthesis and biological evaluation of 1-(5-(2-chloroquinolin-3-yl)-3-phenyl-1H-pyrazol-1-yl)ethanone derivatives as potential antimicrobial agents
title_full Synthesis and biological evaluation of 1-(5-(2-chloroquinolin-3-yl)-3-phenyl-1H-pyrazol-1-yl)ethanone derivatives as potential antimicrobial agents
title_fullStr Synthesis and biological evaluation of 1-(5-(2-chloroquinolin-3-yl)-3-phenyl-1H-pyrazol-1-yl)ethanone derivatives as potential antimicrobial agents
title_full_unstemmed Synthesis and biological evaluation of 1-(5-(2-chloroquinolin-3-yl)-3-phenyl-1H-pyrazol-1-yl)ethanone derivatives as potential antimicrobial agents
title_sort synthesis and biological evaluation of 1-(5-(2-chloroquinolin-3-yl)-3-phenyl-1h-pyrazol-1-yl)ethanone derivatives as potential antimicrobial agents
publisher Elsevier
series Journal of Saudi Chemical Society
issn 1319-6103
publishDate 2015-11-01
description A novel series of 2-Chloroquinoline nucleus clubbed with the pyrazole ring has been synthesized and screened for antibacterial and antifungal activity. The results obtained were promising against both bacterial and fungal strains.   Among the series, compound MB-N was found moderately active against Aspergillus fumigatus, Penicillium notatum and Bacillus subtilis having MIC 48, 46 and 44 μg/ml, respectively whereas compound MB-A was found active against P. notatum, B. subtilis and Escherichia coli having MIC 57, 54 and 43 μg/ml, respectively as compared to standard.
topic Quinoline
Pyrazole
Antibacterial
Antifungal
url http://www.sciencedirect.com/science/article/pii/S1319610313001348
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AT maheshabarmade synthesisandbiologicalevaluationof152chloroquinolin3yl3phenyl1hpyrazol1ylethanonederivativesaspotentialantimicrobialagents
AT anandamahajan synthesisandbiologicalevaluationof152chloroquinolin3yl3phenyl1hpyrazol1ylethanonederivativesaspotentialantimicrobialagents
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