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Novel Antifungal Dimers from the Roots of Taiwania cryptomerioides
Five new dimer compounds, namely Taiwaniacryptodimers A–E (1–5), were isolated from the methanol extract of the roots of Taiwania cryptomerioides. Their structures were established by mean of spectroscopic analysis and comparison of NMR data with those of known analogues. Their antifungal activities...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8779853/ https://www.ncbi.nlm.nih.gov/pubmed/35056749 http://dx.doi.org/10.3390/molecules27020437 |
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author | Cheng, Ming-Jen Wu, Ming-Der Chang, Chao-Lin Chang, Hsun-Shuo Chyu, Chiou-Fung Kuo, Yueh-Hsiung |
author_facet | Cheng, Ming-Jen Wu, Ming-Der Chang, Chao-Lin Chang, Hsun-Shuo Chyu, Chiou-Fung Kuo, Yueh-Hsiung |
author_sort | Cheng, Ming-Jen |
collection | PubMed |
description | Five new dimer compounds, namely Taiwaniacryptodimers A–E (1–5), were isolated from the methanol extract of the roots of Taiwania cryptomerioides. Their structures were established by mean of spectroscopic analysis and comparison of NMR data with those of known analogues. Their antifungal activities were also evaluated. Our results indicated that metabolites 1, 2, 4, and 5 displayed moderate antifungal activities against Aspergillus niger, Penicillium italicum, Candida albicans, and Saccharomyces cerevisiae. |
format | Online Article Text |
id | pubmed-8779853 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-87798532022-01-22 Novel Antifungal Dimers from the Roots of Taiwania cryptomerioides Cheng, Ming-Jen Wu, Ming-Der Chang, Chao-Lin Chang, Hsun-Shuo Chyu, Chiou-Fung Kuo, Yueh-Hsiung Molecules Article Five new dimer compounds, namely Taiwaniacryptodimers A–E (1–5), were isolated from the methanol extract of the roots of Taiwania cryptomerioides. Their structures were established by mean of spectroscopic analysis and comparison of NMR data with those of known analogues. Their antifungal activities were also evaluated. Our results indicated that metabolites 1, 2, 4, and 5 displayed moderate antifungal activities against Aspergillus niger, Penicillium italicum, Candida albicans, and Saccharomyces cerevisiae. MDPI 2022-01-10 /pmc/articles/PMC8779853/ /pubmed/35056749 http://dx.doi.org/10.3390/molecules27020437 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 Cheng, Ming-Jen Wu, Ming-Der Chang, Chao-Lin Chang, Hsun-Shuo Chyu, Chiou-Fung Kuo, Yueh-Hsiung Novel Antifungal Dimers from the Roots of Taiwania cryptomerioides |
title | Novel Antifungal Dimers from the Roots of Taiwania cryptomerioides |
title_full | Novel Antifungal Dimers from the Roots of Taiwania cryptomerioides |
title_fullStr | Novel Antifungal Dimers from the Roots of Taiwania cryptomerioides |
title_full_unstemmed | Novel Antifungal Dimers from the Roots of Taiwania cryptomerioides |
title_short | Novel Antifungal Dimers from the Roots of Taiwania cryptomerioides |
title_sort | novel antifungal dimers from the roots of taiwania cryptomerioides |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8779853/ https://www.ncbi.nlm.nih.gov/pubmed/35056749 http://dx.doi.org/10.3390/molecules27020437 |
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