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Synthesis of novel Schiff bases containing arylpyrimidines as promising antibacterial agents

Pursuing our recent interest regarding the antimicrobial activity of Schiff bases derivatives, we have synthesized a series of 6-(substitutedphenyl)-N'-((E)-(substitutedphenyl)methylidene)-2-methylpyridine-3-carbohydrazides (5a-n) and evaluated their antibacterial activity. Structures of these...

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Detalles Bibliográficos
Autores principales: Nayak, Soukhyarani Gopal, Poojary, Boja
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6709410/
https://www.ncbi.nlm.nih.gov/pubmed/31463406
http://dx.doi.org/10.1016/j.heliyon.2019.e02318
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author Nayak, Soukhyarani Gopal
Poojary, Boja
author_facet Nayak, Soukhyarani Gopal
Poojary, Boja
author_sort Nayak, Soukhyarani Gopal
collection PubMed
description Pursuing our recent interest regarding the antimicrobial activity of Schiff bases derivatives, we have synthesized a series of 6-(substitutedphenyl)-N'-((E)-(substitutedphenyl)methylidene)-2-methylpyridine-3-carbohydrazides (5a-n) and evaluated their antibacterial activity. Structures of these compounds were confirmed by standard studies of FTIR, (1)H NMR, (13)C NMR, MS and elemental analysis. Antibacterial activity of synthesized molecules was tested against Gram-positive (S. aureus and E. faecalis) and Gram-negative (E. coli and P. aeruginosa) bacterial strains. Synthesized compounds showed good antibacterial activity at a lower concentration than standard. Most of the compounds (5a, 5c, 5i, 5j and 5n) are potent against all the tested bacterial strains with MIC values ranging from 1.56-12.5 μg/mL.
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spelling pubmed-67094102019-08-28 Synthesis of novel Schiff bases containing arylpyrimidines as promising antibacterial agents Nayak, Soukhyarani Gopal Poojary, Boja Heliyon Article Pursuing our recent interest regarding the antimicrobial activity of Schiff bases derivatives, we have synthesized a series of 6-(substitutedphenyl)-N'-((E)-(substitutedphenyl)methylidene)-2-methylpyridine-3-carbohydrazides (5a-n) and evaluated their antibacterial activity. Structures of these compounds were confirmed by standard studies of FTIR, (1)H NMR, (13)C NMR, MS and elemental analysis. Antibacterial activity of synthesized molecules was tested against Gram-positive (S. aureus and E. faecalis) and Gram-negative (E. coli and P. aeruginosa) bacterial strains. Synthesized compounds showed good antibacterial activity at a lower concentration than standard. Most of the compounds (5a, 5c, 5i, 5j and 5n) are potent against all the tested bacterial strains with MIC values ranging from 1.56-12.5 μg/mL. Elsevier 2019-08-20 /pmc/articles/PMC6709410/ /pubmed/31463406 http://dx.doi.org/10.1016/j.heliyon.2019.e02318 Text en © 2019 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Nayak, Soukhyarani Gopal
Poojary, Boja
Synthesis of novel Schiff bases containing arylpyrimidines as promising antibacterial agents
title Synthesis of novel Schiff bases containing arylpyrimidines as promising antibacterial agents
title_full Synthesis of novel Schiff bases containing arylpyrimidines as promising antibacterial agents
title_fullStr Synthesis of novel Schiff bases containing arylpyrimidines as promising antibacterial agents
title_full_unstemmed Synthesis of novel Schiff bases containing arylpyrimidines as promising antibacterial agents
title_short Synthesis of novel Schiff bases containing arylpyrimidines as promising antibacterial agents
title_sort synthesis of novel schiff bases containing arylpyrimidines as promising antibacterial agents
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6709410/
https://www.ncbi.nlm.nih.gov/pubmed/31463406
http://dx.doi.org/10.1016/j.heliyon.2019.e02318
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