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Synthesis and Antimicrobial Activity of Some New Substituted Quinoxalines

A number of new symmetrically and asymmetrically 2,3-disubstituted quinoxalines were synthesized through functionalization of 2,3-dichloroquinoxaline (2,3-DCQ) with a variety of sulfur and/or nitrogen nucleophiles. The structures of the obtained compounds were established based on their spectral dat...

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Autores principales: El-Atawy, Mohamed A., Hamed, Ezzat A., Alhadi, Mahjoba, Omar, Alaa Z.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6891733/
https://www.ncbi.nlm.nih.gov/pubmed/31752396
http://dx.doi.org/10.3390/molecules24224198
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author El-Atawy, Mohamed A.
Hamed, Ezzat A.
Alhadi, Mahjoba
Omar, Alaa Z.
author_facet El-Atawy, Mohamed A.
Hamed, Ezzat A.
Alhadi, Mahjoba
Omar, Alaa Z.
author_sort El-Atawy, Mohamed A.
collection PubMed
description A number of new symmetrically and asymmetrically 2,3-disubstituted quinoxalines were synthesized through functionalization of 2,3-dichloroquinoxaline (2,3-DCQ) with a variety of sulfur and/or nitrogen nucleophiles. The structures of the obtained compounds were established based on their spectral data and elemental analysis. The antimicrobial activity for the prepared compounds was investigated against four bacterial species and two fungal strains. The symmetrically disubstituted quinoxalines 2, 3, 4, and 5 displayed the most significant antibacterial activity, while compounds 6a, 6b, and the pentacyclic compound 10 showed considerable antifungal activity. Furthermore, compounds 3f, 6b showed broad antimicrobial spectrum against most of the tested strains.
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spelling pubmed-68917332019-12-12 Synthesis and Antimicrobial Activity of Some New Substituted Quinoxalines El-Atawy, Mohamed A. Hamed, Ezzat A. Alhadi, Mahjoba Omar, Alaa Z. Molecules Article A number of new symmetrically and asymmetrically 2,3-disubstituted quinoxalines were synthesized through functionalization of 2,3-dichloroquinoxaline (2,3-DCQ) with a variety of sulfur and/or nitrogen nucleophiles. The structures of the obtained compounds were established based on their spectral data and elemental analysis. The antimicrobial activity for the prepared compounds was investigated against four bacterial species and two fungal strains. The symmetrically disubstituted quinoxalines 2, 3, 4, and 5 displayed the most significant antibacterial activity, while compounds 6a, 6b, and the pentacyclic compound 10 showed considerable antifungal activity. Furthermore, compounds 3f, 6b showed broad antimicrobial spectrum against most of the tested strains. MDPI 2019-11-19 /pmc/articles/PMC6891733/ /pubmed/31752396 http://dx.doi.org/10.3390/molecules24224198 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
El-Atawy, Mohamed A.
Hamed, Ezzat A.
Alhadi, Mahjoba
Omar, Alaa Z.
Synthesis and Antimicrobial Activity of Some New Substituted Quinoxalines
title Synthesis and Antimicrobial Activity of Some New Substituted Quinoxalines
title_full Synthesis and Antimicrobial Activity of Some New Substituted Quinoxalines
title_fullStr Synthesis and Antimicrobial Activity of Some New Substituted Quinoxalines
title_full_unstemmed Synthesis and Antimicrobial Activity of Some New Substituted Quinoxalines
title_short Synthesis and Antimicrobial Activity of Some New Substituted Quinoxalines
title_sort synthesis and antimicrobial activity of some new substituted quinoxalines
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6891733/
https://www.ncbi.nlm.nih.gov/pubmed/31752396
http://dx.doi.org/10.3390/molecules24224198
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