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Synthesis of novel antibacterial and antifungal quinoxaline derivatives

A series of quinoxaline derivatives were designed, synthesized and evaluated as antimicrobial agents against plant pathogenic bacteria and fungi. Some of these compounds exhibited significant antibacterial and antifungal activities in vitro. Compound 5k displayed good antibacterial activity against...

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Detalles Bibliográficos
Autores principales: Tang, Xuemei, Zhou, Qing, Zhan, Wenliang, Hu, Die, Zhou, Ran, Sun, Nan, Chen, Shuai, Wu, Wenneng, Xue, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8979181/
https://www.ncbi.nlm.nih.gov/pubmed/35425241
http://dx.doi.org/10.1039/d1ra07559d
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author Tang, Xuemei
Zhou, Qing
Zhan, Wenliang
Hu, Die
Zhou, Ran
Sun, Nan
Chen, Shuai
Wu, Wenneng
Xue, Wei
author_facet Tang, Xuemei
Zhou, Qing
Zhan, Wenliang
Hu, Die
Zhou, Ran
Sun, Nan
Chen, Shuai
Wu, Wenneng
Xue, Wei
author_sort Tang, Xuemei
collection PubMed
description A series of quinoxaline derivatives were designed, synthesized and evaluated as antimicrobial agents against plant pathogenic bacteria and fungi. Some of these compounds exhibited significant antibacterial and antifungal activities in vitro. Compound 5k displayed good antibacterial activity against Acidovorax citrulli (Ac). Compounds 5j and 5t exhibited the most potent anti-RS (Rhizoctonia solani) activity, with the corresponding EC(50) values of 8.54 and 12.01 μg mL(−1), respectively, which are superior to that of the commercial azoxystrobin (26.17 μg mL(−1)). Further, the scanning electron microscopy results proved that compound 5j had certain effects on the cell morphology of RS. Moreover, an in vivo bioassay also demonstrated that the anti-RS activity of compound 5j could effectively control rice sheath blight. These results indicate that quinoxaline derivatives could be promising agricultural bactericides and fungicides.
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spelling pubmed-89791812022-04-13 Synthesis of novel antibacterial and antifungal quinoxaline derivatives Tang, Xuemei Zhou, Qing Zhan, Wenliang Hu, Die Zhou, Ran Sun, Nan Chen, Shuai Wu, Wenneng Xue, Wei RSC Adv Chemistry A series of quinoxaline derivatives were designed, synthesized and evaluated as antimicrobial agents against plant pathogenic bacteria and fungi. Some of these compounds exhibited significant antibacterial and antifungal activities in vitro. Compound 5k displayed good antibacterial activity against Acidovorax citrulli (Ac). Compounds 5j and 5t exhibited the most potent anti-RS (Rhizoctonia solani) activity, with the corresponding EC(50) values of 8.54 and 12.01 μg mL(−1), respectively, which are superior to that of the commercial azoxystrobin (26.17 μg mL(−1)). Further, the scanning electron microscopy results proved that compound 5j had certain effects on the cell morphology of RS. Moreover, an in vivo bioassay also demonstrated that the anti-RS activity of compound 5j could effectively control rice sheath blight. These results indicate that quinoxaline derivatives could be promising agricultural bactericides and fungicides. The Royal Society of Chemistry 2022-01-18 /pmc/articles/PMC8979181/ /pubmed/35425241 http://dx.doi.org/10.1039/d1ra07559d Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Tang, Xuemei
Zhou, Qing
Zhan, Wenliang
Hu, Die
Zhou, Ran
Sun, Nan
Chen, Shuai
Wu, Wenneng
Xue, Wei
Synthesis of novel antibacterial and antifungal quinoxaline derivatives
title Synthesis of novel antibacterial and antifungal quinoxaline derivatives
title_full Synthesis of novel antibacterial and antifungal quinoxaline derivatives
title_fullStr Synthesis of novel antibacterial and antifungal quinoxaline derivatives
title_full_unstemmed Synthesis of novel antibacterial and antifungal quinoxaline derivatives
title_short Synthesis of novel antibacterial and antifungal quinoxaline derivatives
title_sort synthesis of novel antibacterial and antifungal quinoxaline derivatives
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8979181/
https://www.ncbi.nlm.nih.gov/pubmed/35425241
http://dx.doi.org/10.1039/d1ra07559d
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