Cargando…
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...
Autores principales: | , , , , , |
---|---|
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 |
_version_ | 1783377576174026752 |
---|---|
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. |
format | Online Article Text |
id | pubmed-6274255 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT liangzhen designsynthesisandantifungalactivityofnovelbenzofurantriazolehybrids AT xuhang designsynthesisandantifungalactivityofnovelbenzofurantriazolehybrids AT tianye designsynthesisandantifungalactivityofnovelbenzofurantriazolehybrids AT guomengbi designsynthesisandantifungalactivityofnovelbenzofurantriazolehybrids AT suxin designsynthesisandantifungalactivityofnovelbenzofurantriazolehybrids AT guochun designsynthesisandantifungalactivityofnovelbenzofurantriazolehybrids |