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Three New Asperentin Derivatives from the Algicolous Fungus Aspergillus sp. F00785
Three new asperentin-type compounds, 6-O-α-d-ribosylasperentin (1) and 6-O-α-d-ribosyl-8-O-methylasperentin (2) and 5-hydroxyl-6-O-methylasperentin (3), along with asperentin (4) and its known analogues (5–9), were isolated from a halotolerant Aspergillus sp. strain F00785, an endotrophic fungus fro...
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/PMC4278214/ https://www.ncbi.nlm.nih.gov/pubmed/25517217 http://dx.doi.org/10.3390/md12125993 |
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author | Tang, Qian Guo, Kai Li, Xiao-Yang Zheng, Xiu-Ying Kong, Xiang-Jian Zheng, Zhong-Hui Xu, Qing-Yan Deng, Xianming |
author_facet | Tang, Qian Guo, Kai Li, Xiao-Yang Zheng, Xiu-Ying Kong, Xiang-Jian Zheng, Zhong-Hui Xu, Qing-Yan Deng, Xianming |
author_sort | Tang, Qian |
collection | PubMed |
description | Three new asperentin-type compounds, 6-O-α-d-ribosylasperentin (1) and 6-O-α-d-ribosyl-8-O-methylasperentin (2) and 5-hydroxyl-6-O-methylasperentin (3), along with asperentin (4) and its known analogues (5–9), were isolated from a halotolerant Aspergillus sp. strain F00785, an endotrophic fungus from marine alga. Their structures were determined using extensive NMR and HRESIMS spectroscopic analysis, including the X-ray crystallographic data for the assignment of the absolute configurations of compound 9. Compound 4 exhibited highly potent inhibitory activity against crop pathogens, Colletotrichum gleosporioides Penz. and Colletotrichum gleosporioides (Penz.) Sacc. |
format | Online Article Text |
id | pubmed-4278214 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-42782142015-01-08 Three New Asperentin Derivatives from the Algicolous Fungus Aspergillus sp. F00785 Tang, Qian Guo, Kai Li, Xiao-Yang Zheng, Xiu-Ying Kong, Xiang-Jian Zheng, Zhong-Hui Xu, Qing-Yan Deng, Xianming Mar Drugs Article Three new asperentin-type compounds, 6-O-α-d-ribosylasperentin (1) and 6-O-α-d-ribosyl-8-O-methylasperentin (2) and 5-hydroxyl-6-O-methylasperentin (3), along with asperentin (4) and its known analogues (5–9), were isolated from a halotolerant Aspergillus sp. strain F00785, an endotrophic fungus from marine alga. Their structures were determined using extensive NMR and HRESIMS spectroscopic analysis, including the X-ray crystallographic data for the assignment of the absolute configurations of compound 9. Compound 4 exhibited highly potent inhibitory activity against crop pathogens, Colletotrichum gleosporioides Penz. and Colletotrichum gleosporioides (Penz.) Sacc. MDPI 2014-12-15 /pmc/articles/PMC4278214/ /pubmed/25517217 http://dx.doi.org/10.3390/md12125993 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/4.0/). |
spellingShingle | Article Tang, Qian Guo, Kai Li, Xiao-Yang Zheng, Xiu-Ying Kong, Xiang-Jian Zheng, Zhong-Hui Xu, Qing-Yan Deng, Xianming Three New Asperentin Derivatives from the Algicolous Fungus Aspergillus sp. F00785 |
title | Three New Asperentin Derivatives from the Algicolous Fungus Aspergillus sp. F00785 |
title_full | Three New Asperentin Derivatives from the Algicolous Fungus Aspergillus sp. F00785 |
title_fullStr | Three New Asperentin Derivatives from the Algicolous Fungus Aspergillus sp. F00785 |
title_full_unstemmed | Three New Asperentin Derivatives from the Algicolous Fungus Aspergillus sp. F00785 |
title_short | Three New Asperentin Derivatives from the Algicolous Fungus Aspergillus sp. F00785 |
title_sort | three new asperentin derivatives from the algicolous fungus aspergillus sp. f00785 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4278214/ https://www.ncbi.nlm.nih.gov/pubmed/25517217 http://dx.doi.org/10.3390/md12125993 |
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