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Synthesis and Anti-Bacterial Activities of Some Novel Schiff Bases Derived from Aminophenazone

A series of 1,5-dimethyl-2-phenyl-1,2-dihydro-3H-pyrazol-3-one-containing Schiff bases were synthesized, characterized and screened for their antibacterial activities. The structures of the synthesized compounds were established by spectroscopic (FT-IR, (1)H-NMR, (13)C-NMR, MS) and elemental analyse...

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Autores principales: Asiri, Abdullah M., Khan, Salman A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259180/
https://www.ncbi.nlm.nih.gov/pubmed/20938399
http://dx.doi.org/10.3390/molecules15106850
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author Asiri, Abdullah M.
Khan, Salman A
author_facet Asiri, Abdullah M.
Khan, Salman A
author_sort Asiri, Abdullah M.
collection PubMed
description A series of 1,5-dimethyl-2-phenyl-1,2-dihydro-3H-pyrazol-3-one-containing Schiff bases were synthesized, characterized and screened for their antibacterial activities. The structures of the synthesized compounds were established by spectroscopic (FT-IR, (1)H-NMR, (13)C-NMR, MS) and elemental analyses. The anti-bacterial activities (with MIC values) of compounds were evaluated. The anti-bacterial screening results reveal that among the six compounds screened, four compounds showed moderate to good anti-bacterial activity. Among the tested compounds, the most effective compounds against four bacterial strains, viz. Escherichia coli, Staphylococcus aureus, Salmonella typhimurium and Streptococcus pyogenes, are [(2-Chlorobenzylidene)amino]-1,5-dimethyl-2-phenyl-1,2-dihydropyrazol-3-one (4) and [(1,5-Dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazol-4-ylimino)methyl]benzonitrile(5) with MIC values of 6.25 μg/mL.
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spelling pubmed-62591802018-12-06 Synthesis and Anti-Bacterial Activities of Some Novel Schiff Bases Derived from Aminophenazone Asiri, Abdullah M. Khan, Salman A Molecules Communication A series of 1,5-dimethyl-2-phenyl-1,2-dihydro-3H-pyrazol-3-one-containing Schiff bases were synthesized, characterized and screened for their antibacterial activities. The structures of the synthesized compounds were established by spectroscopic (FT-IR, (1)H-NMR, (13)C-NMR, MS) and elemental analyses. The anti-bacterial activities (with MIC values) of compounds were evaluated. The anti-bacterial screening results reveal that among the six compounds screened, four compounds showed moderate to good anti-bacterial activity. Among the tested compounds, the most effective compounds against four bacterial strains, viz. Escherichia coli, Staphylococcus aureus, Salmonella typhimurium and Streptococcus pyogenes, are [(2-Chlorobenzylidene)amino]-1,5-dimethyl-2-phenyl-1,2-dihydropyrazol-3-one (4) and [(1,5-Dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazol-4-ylimino)methyl]benzonitrile(5) with MIC values of 6.25 μg/mL. MDPI 2010-10-08 /pmc/articles/PMC6259180/ /pubmed/20938399 http://dx.doi.org/10.3390/molecules15106850 Text en © 2010 by the authors; http://creativecommons.org/licenses/by/3.0/ licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Communication
Asiri, Abdullah M.
Khan, Salman A
Synthesis and Anti-Bacterial Activities of Some Novel Schiff Bases Derived from Aminophenazone
title Synthesis and Anti-Bacterial Activities of Some Novel Schiff Bases Derived from Aminophenazone
title_full Synthesis and Anti-Bacterial Activities of Some Novel Schiff Bases Derived from Aminophenazone
title_fullStr Synthesis and Anti-Bacterial Activities of Some Novel Schiff Bases Derived from Aminophenazone
title_full_unstemmed Synthesis and Anti-Bacterial Activities of Some Novel Schiff Bases Derived from Aminophenazone
title_short Synthesis and Anti-Bacterial Activities of Some Novel Schiff Bases Derived from Aminophenazone
title_sort synthesis and anti-bacterial activities of some novel schiff bases derived from aminophenazone
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259180/
https://www.ncbi.nlm.nih.gov/pubmed/20938399
http://dx.doi.org/10.3390/molecules15106850
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