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Discovery of 4-nitro-3-phenylisoxazole derivatives as potent antibacterial agents derived from the studies of [3 + 2] cycloaddition
Polysubstituted phenylisoxazoles were designed and synthesized to discover new antibacterial agents via [3 + 2] cycloaddition. Thirty-five compounds with a phenylisoxazole scaffold were characterized by NMR, HRMS, and X-ray techniques. After being evaluated against Xanthomonas oryzae (Xoo), Pseudomo...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9455768/ https://www.ncbi.nlm.nih.gov/pubmed/36199305 http://dx.doi.org/10.1039/d2ra05009a |
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author | Zhang, Yan Long, Zhiwu Yan, Longjia Liu, Li Yang, Lan Le, Yi |
author_facet | Zhang, Yan Long, Zhiwu Yan, Longjia Liu, Li Yang, Lan Le, Yi |
author_sort | Zhang, Yan |
collection | PubMed |
description | Polysubstituted phenylisoxazoles were designed and synthesized to discover new antibacterial agents via [3 + 2] cycloaddition. Thirty-five compounds with a phenylisoxazole scaffold were characterized by NMR, HRMS, and X-ray techniques. After being evaluated against Xanthomonas oryzae (Xoo), Pseudomonas syringae (Psa), and Xanthomonas axonopodis (Xac), 4-nitro-3-phenylisoxazole derivatives were found to better antibacterial activities. Further studies have shown that the EC(50) values of these compounds were much better than that of the positive control, bismerthiazol. |
format | Online Article Text |
id | pubmed-9455768 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-94557682022-10-04 Discovery of 4-nitro-3-phenylisoxazole derivatives as potent antibacterial agents derived from the studies of [3 + 2] cycloaddition Zhang, Yan Long, Zhiwu Yan, Longjia Liu, Li Yang, Lan Le, Yi RSC Adv Chemistry Polysubstituted phenylisoxazoles were designed and synthesized to discover new antibacterial agents via [3 + 2] cycloaddition. Thirty-five compounds with a phenylisoxazole scaffold were characterized by NMR, HRMS, and X-ray techniques. After being evaluated against Xanthomonas oryzae (Xoo), Pseudomonas syringae (Psa), and Xanthomonas axonopodis (Xac), 4-nitro-3-phenylisoxazole derivatives were found to better antibacterial activities. Further studies have shown that the EC(50) values of these compounds were much better than that of the positive control, bismerthiazol. The Royal Society of Chemistry 2022-09-08 /pmc/articles/PMC9455768/ /pubmed/36199305 http://dx.doi.org/10.1039/d2ra05009a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Zhang, Yan Long, Zhiwu Yan, Longjia Liu, Li Yang, Lan Le, Yi Discovery of 4-nitro-3-phenylisoxazole derivatives as potent antibacterial agents derived from the studies of [3 + 2] cycloaddition |
title | Discovery of 4-nitro-3-phenylisoxazole derivatives as potent antibacterial agents derived from the studies of [3 + 2] cycloaddition |
title_full | Discovery of 4-nitro-3-phenylisoxazole derivatives as potent antibacterial agents derived from the studies of [3 + 2] cycloaddition |
title_fullStr | Discovery of 4-nitro-3-phenylisoxazole derivatives as potent antibacterial agents derived from the studies of [3 + 2] cycloaddition |
title_full_unstemmed | Discovery of 4-nitro-3-phenylisoxazole derivatives as potent antibacterial agents derived from the studies of [3 + 2] cycloaddition |
title_short | Discovery of 4-nitro-3-phenylisoxazole derivatives as potent antibacterial agents derived from the studies of [3 + 2] cycloaddition |
title_sort | discovery of 4-nitro-3-phenylisoxazole derivatives as potent antibacterial agents derived from the studies of [3 + 2] cycloaddition |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9455768/ https://www.ncbi.nlm.nih.gov/pubmed/36199305 http://dx.doi.org/10.1039/d2ra05009a |
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