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Three New Oblongolides from Phomopsis sp. XZ-01, an Endophytic Fungus from Camptotheca acuminate
Four new metabolites, including three new oblongolides named C1, P1, and X1 (1-3) and 6-hydroxyphomodiol (10), along with eight known compounds – oblongolides B (4), C (5), D (6), O (7), P (8) and U (9), (3R,4aR,5S,6R)-6-hydroxy-5-methylramulosin (11), and (3R)-5-methylmellein (12) – were isolated f...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6260605/ https://www.ncbi.nlm.nih.gov/pubmed/21512443 http://dx.doi.org/10.3390/molecules16043351 |
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author | Lin, Ting Wang, Guang Hui Lin, Xiang Hu, Zhi Yu Chen, Quan Cheng Xu, Yang Zhang, Xiao Kun Chen, Hai Feng |
author_facet | Lin, Ting Wang, Guang Hui Lin, Xiang Hu, Zhi Yu Chen, Quan Cheng Xu, Yang Zhang, Xiao Kun Chen, Hai Feng |
author_sort | Lin, Ting |
collection | PubMed |
description | Four new metabolites, including three new oblongolides named C1, P1, and X1 (1-3) and 6-hydroxyphomodiol (10), along with eight known compounds – oblongolides B (4), C (5), D (6), O (7), P (8) and U (9), (3R,4aR,5S,6R)-6-hydroxy-5-methylramulosin (11), and (3R)-5-methylmellein (12) – were isolated from the endophytic fungal strain Phomopsis sp. XZ-01 of Camptotheca acuminate. Their structures were elucidated by spectroscopic analyses, including (1)H- and (13)C-NMR, 2D NMR (HSQC, HMBC, (1)H-(1)H COSY and NOESY) and HR-FT-MS. Cytotoxic activities of these compounds were evaluated. Some of them showed weak selective activities. |
format | Online Article Text |
id | pubmed-6260605 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62606052018-12-10 Three New Oblongolides from Phomopsis sp. XZ-01, an Endophytic Fungus from Camptotheca acuminate Lin, Ting Wang, Guang Hui Lin, Xiang Hu, Zhi Yu Chen, Quan Cheng Xu, Yang Zhang, Xiao Kun Chen, Hai Feng Molecules Article Four new metabolites, including three new oblongolides named C1, P1, and X1 (1-3) and 6-hydroxyphomodiol (10), along with eight known compounds – oblongolides B (4), C (5), D (6), O (7), P (8) and U (9), (3R,4aR,5S,6R)-6-hydroxy-5-methylramulosin (11), and (3R)-5-methylmellein (12) – were isolated from the endophytic fungal strain Phomopsis sp. XZ-01 of Camptotheca acuminate. Their structures were elucidated by spectroscopic analyses, including (1)H- and (13)C-NMR, 2D NMR (HSQC, HMBC, (1)H-(1)H COSY and NOESY) and HR-FT-MS. Cytotoxic activities of these compounds were evaluated. Some of them showed weak selective activities. MDPI 2011-04-19 /pmc/articles/PMC6260605/ /pubmed/21512443 http://dx.doi.org/10.3390/molecules16043351 Text en © 2011 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 Lin, Ting Wang, Guang Hui Lin, Xiang Hu, Zhi Yu Chen, Quan Cheng Xu, Yang Zhang, Xiao Kun Chen, Hai Feng Three New Oblongolides from Phomopsis sp. XZ-01, an Endophytic Fungus from Camptotheca acuminate |
title | Three New Oblongolides from Phomopsis sp. XZ-01, an Endophytic Fungus from Camptotheca acuminate |
title_full | Three New Oblongolides from Phomopsis sp. XZ-01, an Endophytic Fungus from Camptotheca acuminate |
title_fullStr | Three New Oblongolides from Phomopsis sp. XZ-01, an Endophytic Fungus from Camptotheca acuminate |
title_full_unstemmed | Three New Oblongolides from Phomopsis sp. XZ-01, an Endophytic Fungus from Camptotheca acuminate |
title_short | Three New Oblongolides from Phomopsis sp. XZ-01, an Endophytic Fungus from Camptotheca acuminate |
title_sort | three new oblongolides from phomopsis sp. xz-01, an endophytic fungus from camptotheca acuminate |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6260605/ https://www.ncbi.nlm.nih.gov/pubmed/21512443 http://dx.doi.org/10.3390/molecules16043351 |
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