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Design, synthesis, and antifungal activities of novel triazole derivatives containing the benzyl group
In previous studies undertaken by our group, a series of 1-(1H-1,2,4-triazole-1-yl)-2-(2,4-difluorophenyl)-3-substituted-2-propanols (1a–r), which were analogs of fluconazole, was designed and synthesized by click chemistry. In the study reported here, the in vitro antifungal activities of all the t...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4362653/ https://www.ncbi.nlm.nih.gov/pubmed/25792806 http://dx.doi.org/10.2147/DDDT.S74989 |
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author | Xu, Kehan Huang, Lei Xu, Zheng Wang, Yanwei Bai, Guojing Wu, Qiuye Wang, Xiaoyan Yu, Shichong Jiang, Yuanying |
author_facet | Xu, Kehan Huang, Lei Xu, Zheng Wang, Yanwei Bai, Guojing Wu, Qiuye Wang, Xiaoyan Yu, Shichong Jiang, Yuanying |
author_sort | Xu, Kehan |
collection | PubMed |
description | In previous studies undertaken by our group, a series of 1-(1H-1,2,4-triazole-1-yl)-2-(2,4-difluorophenyl)-3-substituted-2-propanols (1a–r), which were analogs of fluconazole, was designed and synthesized by click chemistry. In the study reported here, the in vitro antifungal activities of all the target compounds were evaluated against eight human pathogenic fungi. Compounds 1a, 1q, and 1r showed the more antifungal activity than the others. |
format | Online Article Text |
id | pubmed-4362653 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-43626532015-03-19 Design, synthesis, and antifungal activities of novel triazole derivatives containing the benzyl group Xu, Kehan Huang, Lei Xu, Zheng Wang, Yanwei Bai, Guojing Wu, Qiuye Wang, Xiaoyan Yu, Shichong Jiang, Yuanying Drug Des Devel Ther Original Research In previous studies undertaken by our group, a series of 1-(1H-1,2,4-triazole-1-yl)-2-(2,4-difluorophenyl)-3-substituted-2-propanols (1a–r), which were analogs of fluconazole, was designed and synthesized by click chemistry. In the study reported here, the in vitro antifungal activities of all the target compounds were evaluated against eight human pathogenic fungi. Compounds 1a, 1q, and 1r showed the more antifungal activity than the others. Dove Medical Press 2015-03-11 /pmc/articles/PMC4362653/ /pubmed/25792806 http://dx.doi.org/10.2147/DDDT.S74989 Text en © 2015 Xu et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Xu, Kehan Huang, Lei Xu, Zheng Wang, Yanwei Bai, Guojing Wu, Qiuye Wang, Xiaoyan Yu, Shichong Jiang, Yuanying Design, synthesis, and antifungal activities of novel triazole derivatives containing the benzyl group |
title | Design, synthesis, and antifungal activities of novel triazole derivatives containing the benzyl group |
title_full | Design, synthesis, and antifungal activities of novel triazole derivatives containing the benzyl group |
title_fullStr | Design, synthesis, and antifungal activities of novel triazole derivatives containing the benzyl group |
title_full_unstemmed | Design, synthesis, and antifungal activities of novel triazole derivatives containing the benzyl group |
title_short | Design, synthesis, and antifungal activities of novel triazole derivatives containing the benzyl group |
title_sort | design, synthesis, and antifungal activities of novel triazole derivatives containing the benzyl group |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4362653/ https://www.ncbi.nlm.nih.gov/pubmed/25792806 http://dx.doi.org/10.2147/DDDT.S74989 |
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