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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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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. |
format | Online Article Text |
id | pubmed-6891733 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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