Cargando…
Synthesis and Antifungal Activity of Chimonanthus praecox Derivatives
To search for efficient agricultural antifungal lead compounds, 39 Chimonanthus praecox derivatives were designed, synthesized, and evaluated for their antifungal activities. The structures of target compounds were fully characterized by (1)H NMR, (13)C NMR, and MS spectra. The preliminary bioassays...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9457717/ https://www.ncbi.nlm.nih.gov/pubmed/36080337 http://dx.doi.org/10.3390/molecules27175570 |
_version_ | 1784786124456067072 |
---|---|
author | Chen, Jinfeng Yang, Yimou Zhou, Yujie Wei, Yang Zhu, Rui Zheng, Shaojun |
author_facet | Chen, Jinfeng Yang, Yimou Zhou, Yujie Wei, Yang Zhu, Rui Zheng, Shaojun |
author_sort | Chen, Jinfeng |
collection | PubMed |
description | To search for efficient agricultural antifungal lead compounds, 39 Chimonanthus praecox derivatives were designed, synthesized, and evaluated for their antifungal activities. The structures of target compounds were fully characterized by (1)H NMR, (13)C NMR, and MS spectra. The preliminary bioassays revealed that some compounds exhibited excellent antifungal activities in vitro. For example, the minimum inhibitory concentration (MIC) of compound b15 against Phytophthora infestans was 1.95 µg mL(−1), and the minimum inhibitory concentration (MIC) of compound b17 against Sclerotinia sclerotiorum was 1.95 µg mL(−1). Therefore, compounds b15 and b17 were identified as the most promising candidates for further study. |
format | Online Article Text |
id | pubmed-9457717 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-94577172022-09-09 Synthesis and Antifungal Activity of Chimonanthus praecox Derivatives Chen, Jinfeng Yang, Yimou Zhou, Yujie Wei, Yang Zhu, Rui Zheng, Shaojun Molecules Article To search for efficient agricultural antifungal lead compounds, 39 Chimonanthus praecox derivatives were designed, synthesized, and evaluated for their antifungal activities. The structures of target compounds were fully characterized by (1)H NMR, (13)C NMR, and MS spectra. The preliminary bioassays revealed that some compounds exhibited excellent antifungal activities in vitro. For example, the minimum inhibitory concentration (MIC) of compound b15 against Phytophthora infestans was 1.95 µg mL(−1), and the minimum inhibitory concentration (MIC) of compound b17 against Sclerotinia sclerotiorum was 1.95 µg mL(−1). Therefore, compounds b15 and b17 were identified as the most promising candidates for further study. MDPI 2022-08-30 /pmc/articles/PMC9457717/ /pubmed/36080337 http://dx.doi.org/10.3390/molecules27175570 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Chen, Jinfeng Yang, Yimou Zhou, Yujie Wei, Yang Zhu, Rui Zheng, Shaojun Synthesis and Antifungal Activity of Chimonanthus praecox Derivatives |
title | Synthesis and Antifungal Activity of Chimonanthus praecox Derivatives |
title_full | Synthesis and Antifungal Activity of Chimonanthus praecox Derivatives |
title_fullStr | Synthesis and Antifungal Activity of Chimonanthus praecox Derivatives |
title_full_unstemmed | Synthesis and Antifungal Activity of Chimonanthus praecox Derivatives |
title_short | Synthesis and Antifungal Activity of Chimonanthus praecox Derivatives |
title_sort | synthesis and antifungal activity of chimonanthus praecox derivatives |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9457717/ https://www.ncbi.nlm.nih.gov/pubmed/36080337 http://dx.doi.org/10.3390/molecules27175570 |
work_keys_str_mv | AT chenjinfeng synthesisandantifungalactivityofchimonanthuspraecoxderivatives AT yangyimou synthesisandantifungalactivityofchimonanthuspraecoxderivatives AT zhouyujie synthesisandantifungalactivityofchimonanthuspraecoxderivatives AT weiyang synthesisandantifungalactivityofchimonanthuspraecoxderivatives AT zhurui synthesisandantifungalactivityofchimonanthuspraecoxderivatives AT zhengshaojun synthesisandantifungalactivityofchimonanthuspraecoxderivatives |