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Design, Synthesis and Antifungal Activity of Novel Benzofuran-Triazole Hybrids

A series of novel benzofuran-triazole hybrids was designed and synthesized by click chemistry, and their structures were characterized by HRMS, FTIR and NMR. The in vitro antifungal activity of target compounds was evaluated using the microdilution broth method against five strains of pathogenic fun...

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Detalles Bibliográficos
Autores principales: Liang, Zhen, Xu, Hang, Tian, Ye, Guo, Mengbi, Su, Xin, Guo, Chun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6274255/
https://www.ncbi.nlm.nih.gov/pubmed/27338311
http://dx.doi.org/10.3390/molecules21060732
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author Liang, Zhen
Xu, Hang
Tian, Ye
Guo, Mengbi
Su, Xin
Guo, Chun
author_facet Liang, Zhen
Xu, Hang
Tian, Ye
Guo, Mengbi
Su, Xin
Guo, Chun
author_sort Liang, Zhen
collection PubMed
description A series of novel benzofuran-triazole hybrids was designed and synthesized by click chemistry, and their structures were characterized by HRMS, FTIR and NMR. The in vitro antifungal activity of target compounds was evaluated using the microdilution broth method against five strains of pathogenic fungi. The result indicated that the target compounds exhibited moderate to satisfactory activity. Furthermore, molecular docking was performed to investigate the binding affinities and interaction modes between the target compound and N-myristoyltransferase. Based on the results, preliminary structure activity relationships (SARs) were summarized to serve as a foundation for further investigation.
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spelling pubmed-62742552018-12-28 Design, Synthesis and Antifungal Activity of Novel Benzofuran-Triazole Hybrids Liang, Zhen Xu, Hang Tian, Ye Guo, Mengbi Su, Xin Guo, Chun Molecules Article A series of novel benzofuran-triazole hybrids was designed and synthesized by click chemistry, and their structures were characterized by HRMS, FTIR and NMR. The in vitro antifungal activity of target compounds was evaluated using the microdilution broth method against five strains of pathogenic fungi. The result indicated that the target compounds exhibited moderate to satisfactory activity. Furthermore, molecular docking was performed to investigate the binding affinities and interaction modes between the target compound and N-myristoyltransferase. Based on the results, preliminary structure activity relationships (SARs) were summarized to serve as a foundation for further investigation. MDPI 2016-06-07 /pmc/articles/PMC6274255/ /pubmed/27338311 http://dx.doi.org/10.3390/molecules21060732 Text en © 2016 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
Liang, Zhen
Xu, Hang
Tian, Ye
Guo, Mengbi
Su, Xin
Guo, Chun
Design, Synthesis and Antifungal Activity of Novel Benzofuran-Triazole Hybrids
title Design, Synthesis and Antifungal Activity of Novel Benzofuran-Triazole Hybrids
title_full Design, Synthesis and Antifungal Activity of Novel Benzofuran-Triazole Hybrids
title_fullStr Design, Synthesis and Antifungal Activity of Novel Benzofuran-Triazole Hybrids
title_full_unstemmed Design, Synthesis and Antifungal Activity of Novel Benzofuran-Triazole Hybrids
title_short Design, Synthesis and Antifungal Activity of Novel Benzofuran-Triazole Hybrids
title_sort design, synthesis and antifungal activity of novel benzofuran-triazole hybrids
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6274255/
https://www.ncbi.nlm.nih.gov/pubmed/27338311
http://dx.doi.org/10.3390/molecules21060732
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