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Characterization of a New Sesquiterpene and Antifungal Activities of Chemical Constituents from Dryopteris fragrans (L.) Schott
One new sesquiterpene and six known compounds were isolated from Dryopteris fragrans (L.) Schot. They were identified as 3-O-β-D-glucopyranosylalbicanol-11-O-β-D-glucopyranoside (1), dihydroconiferylalcohol (2), (E)-3-(4-hydroxyphenyl)acrylic acid (3), esculetin (4), 5,7-dihydroxy-2-hydroxymethylchr...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272047/ https://www.ncbi.nlm.nih.gov/pubmed/24451246 http://dx.doi.org/10.3390/molecules19010507 |
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author | Huang, Yu-Hong Zeng, Wei-Min Li, Guo-Yu Liu, Guo-Qing Zhao, Dan-Dan Wang, Jing Zhang, Yan-Long |
author_facet | Huang, Yu-Hong Zeng, Wei-Min Li, Guo-Yu Liu, Guo-Qing Zhao, Dan-Dan Wang, Jing Zhang, Yan-Long |
author_sort | Huang, Yu-Hong |
collection | PubMed |
description | One new sesquiterpene and six known compounds were isolated from Dryopteris fragrans (L.) Schot. They were identified as 3-O-β-D-glucopyranosylalbicanol-11-O-β-D-glucopyranoside (1), dihydroconiferylalcohol (2), (E)-3-(4-hydroxyphenyl)acrylic acid (3), esculetin (4), 5,7-dihydroxy-2-hydroxymethylchromone (5), eriodictyol (6) and isoorientin (7) by UV, MS, 1D-NMR and 2D-NMR spectroscopy. The antifungal activities of the seven isolated compounds were screened. Compounds 2, 3, 4 and 5 showed obvious activities against Microsporum canis and Epidermophyton floccosum. |
format | Online Article Text |
id | pubmed-6272047 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62720472018-12-20 Characterization of a New Sesquiterpene and Antifungal Activities of Chemical Constituents from Dryopteris fragrans (L.) Schott Huang, Yu-Hong Zeng, Wei-Min Li, Guo-Yu Liu, Guo-Qing Zhao, Dan-Dan Wang, Jing Zhang, Yan-Long Molecules Article One new sesquiterpene and six known compounds were isolated from Dryopteris fragrans (L.) Schot. They were identified as 3-O-β-D-glucopyranosylalbicanol-11-O-β-D-glucopyranoside (1), dihydroconiferylalcohol (2), (E)-3-(4-hydroxyphenyl)acrylic acid (3), esculetin (4), 5,7-dihydroxy-2-hydroxymethylchromone (5), eriodictyol (6) and isoorientin (7) by UV, MS, 1D-NMR and 2D-NMR spectroscopy. The antifungal activities of the seven isolated compounds were screened. Compounds 2, 3, 4 and 5 showed obvious activities against Microsporum canis and Epidermophyton floccosum. MDPI 2014-01-02 /pmc/articles/PMC6272047/ /pubmed/24451246 http://dx.doi.org/10.3390/molecules19010507 Text en © 2014 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 license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Huang, Yu-Hong Zeng, Wei-Min Li, Guo-Yu Liu, Guo-Qing Zhao, Dan-Dan Wang, Jing Zhang, Yan-Long Characterization of a New Sesquiterpene and Antifungal Activities of Chemical Constituents from Dryopteris fragrans (L.) Schott |
title | Characterization of a New Sesquiterpene and Antifungal Activities of Chemical Constituents from Dryopteris fragrans (L.) Schott |
title_full | Characterization of a New Sesquiterpene and Antifungal Activities of Chemical Constituents from Dryopteris fragrans (L.) Schott |
title_fullStr | Characterization of a New Sesquiterpene and Antifungal Activities of Chemical Constituents from Dryopteris fragrans (L.) Schott |
title_full_unstemmed | Characterization of a New Sesquiterpene and Antifungal Activities of Chemical Constituents from Dryopteris fragrans (L.) Schott |
title_short | Characterization of a New Sesquiterpene and Antifungal Activities of Chemical Constituents from Dryopteris fragrans (L.) Schott |
title_sort | characterization of a new sesquiterpene and antifungal activities of chemical constituents from dryopteris fragrans (l.) schott |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272047/ https://www.ncbi.nlm.nih.gov/pubmed/24451246 http://dx.doi.org/10.3390/molecules19010507 |
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