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Chemical Constituents of a Marine-Derived Endophytic Fungus Penicillium commune G2M
Cultivation of the endophytic fungus Penicillium commune, which was isolated from the semi-mangrove plant Hibiscus tiliaceus, afforded one new compound 1-O-(2,4-dihydroxy-6-methylbenzoyl)-glycerol (1) along with thirteen known products, including 1-O-acetylglycerol (2), N-acetyltryptophan (3), 3-ind...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257498/ https://www.ncbi.nlm.nih.gov/pubmed/20657476 http://dx.doi.org/10.3390/molecules15053270 |
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author | Yan, Hui-Jiao Gao, Shu-Shan Li, Chun-Shun Li, Xiao-Ming Wang, Bin-Gui |
author_facet | Yan, Hui-Jiao Gao, Shu-Shan Li, Chun-Shun Li, Xiao-Ming Wang, Bin-Gui |
author_sort | Yan, Hui-Jiao |
collection | PubMed |
description | Cultivation of the endophytic fungus Penicillium commune, which was isolated from the semi-mangrove plant Hibiscus tiliaceus, afforded one new compound 1-O-(2,4-dihydroxy-6-methylbenzoyl)-glycerol (1) along with thirteen known products, including 1-O-acetylglycerol (2), N-acetyltryptophan (3), 3-indolylacetic acid methyl ester (4), 1-(2,4-dihydroxy-3,5-dimethylphenyl)ethanone (5), 2-(2,5-dihydroxyphenyl)acetic acid (6), (4R,5S)-5-hydroxyhexan-4-olide (7), thymidine (8), uracil (9), thymine (10), ergosterol (11), β-sitosterol (12), β-daucosterol (13), and ergosta-7,22-dien-3β,5α,6β-triol (14). The structures of these compounds were established by detailed NMR spectroscopic analysis, as well as by comparison with literature data or with authentic samples. |
format | Online Article Text |
id | pubmed-6257498 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62574982019-01-02 Chemical Constituents of a Marine-Derived Endophytic Fungus Penicillium commune G2M Yan, Hui-Jiao Gao, Shu-Shan Li, Chun-Shun Li, Xiao-Ming Wang, Bin-Gui Molecules Article Cultivation of the endophytic fungus Penicillium commune, which was isolated from the semi-mangrove plant Hibiscus tiliaceus, afforded one new compound 1-O-(2,4-dihydroxy-6-methylbenzoyl)-glycerol (1) along with thirteen known products, including 1-O-acetylglycerol (2), N-acetyltryptophan (3), 3-indolylacetic acid methyl ester (4), 1-(2,4-dihydroxy-3,5-dimethylphenyl)ethanone (5), 2-(2,5-dihydroxyphenyl)acetic acid (6), (4R,5S)-5-hydroxyhexan-4-olide (7), thymidine (8), uracil (9), thymine (10), ergosterol (11), β-sitosterol (12), β-daucosterol (13), and ergosta-7,22-dien-3β,5α,6β-triol (14). The structures of these compounds were established by detailed NMR spectroscopic analysis, as well as by comparison with literature data or with authentic samples. MDPI 2010-05-04 /pmc/articles/PMC6257498/ /pubmed/20657476 http://dx.doi.org/10.3390/molecules15053270 Text en © 2010 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 Yan, Hui-Jiao Gao, Shu-Shan Li, Chun-Shun Li, Xiao-Ming Wang, Bin-Gui Chemical Constituents of a Marine-Derived Endophytic Fungus Penicillium commune G2M |
title | Chemical Constituents of a Marine-Derived Endophytic Fungus Penicillium commune G2M |
title_full | Chemical Constituents of a Marine-Derived Endophytic Fungus Penicillium commune G2M |
title_fullStr | Chemical Constituents of a Marine-Derived Endophytic Fungus Penicillium commune G2M |
title_full_unstemmed | Chemical Constituents of a Marine-Derived Endophytic Fungus Penicillium commune G2M |
title_short | Chemical Constituents of a Marine-Derived Endophytic Fungus Penicillium commune G2M |
title_sort | chemical constituents of a marine-derived endophytic fungus penicillium commune g2m |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257498/ https://www.ncbi.nlm.nih.gov/pubmed/20657476 http://dx.doi.org/10.3390/molecules15053270 |
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