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Myrothecols G and H, Two New Analogues of the Marine-Derived Quinone Sesquiterpene Penicilliumin A
Two new quinone sesquiterpenes named myrothecols G and H (1 and 2), a pair of C-1′ diastereomers of 13-hydroxyl penicilliumin A, were isolated from the mycelia solid cultures of Myrothecium sp. SC0265. Their structures, including the absolute configurations, were established on the basis of the spec...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4483633/ https://www.ncbi.nlm.nih.gov/pubmed/26023841 http://dx.doi.org/10.3390/md13063360 |
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author | Fu, Ying Wu, Ping Xue, Jinghua Li, Hanxiang Wei, Xiaoyi |
author_facet | Fu, Ying Wu, Ping Xue, Jinghua Li, Hanxiang Wei, Xiaoyi |
author_sort | Fu, Ying |
collection | PubMed |
description | Two new quinone sesquiterpenes named myrothecols G and H (1 and 2), a pair of C-1′ diastereomers of 13-hydroxyl penicilliumin A, were isolated from the mycelia solid cultures of Myrothecium sp. SC0265. Their structures, including the absolute configurations, were established on the basis of the spectroscopic data combining with the theoretical conformational analysis. The cytotoxic activities of 1 and 2 were tested against a panel of human tumor cell lines. |
format | Online Article Text |
id | pubmed-4483633 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-44836332015-06-30 Myrothecols G and H, Two New Analogues of the Marine-Derived Quinone Sesquiterpene Penicilliumin A Fu, Ying Wu, Ping Xue, Jinghua Li, Hanxiang Wei, Xiaoyi Mar Drugs Article Two new quinone sesquiterpenes named myrothecols G and H (1 and 2), a pair of C-1′ diastereomers of 13-hydroxyl penicilliumin A, were isolated from the mycelia solid cultures of Myrothecium sp. SC0265. Their structures, including the absolute configurations, were established on the basis of the spectroscopic data combining with the theoretical conformational analysis. The cytotoxic activities of 1 and 2 were tested against a panel of human tumor cell lines. MDPI 2015-05-27 /pmc/articles/PMC4483633/ /pubmed/26023841 http://dx.doi.org/10.3390/md13063360 Text en © 2015 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 Fu, Ying Wu, Ping Xue, Jinghua Li, Hanxiang Wei, Xiaoyi Myrothecols G and H, Two New Analogues of the Marine-Derived Quinone Sesquiterpene Penicilliumin A |
title | Myrothecols G and H, Two New Analogues of the Marine-Derived Quinone Sesquiterpene Penicilliumin A |
title_full | Myrothecols G and H, Two New Analogues of the Marine-Derived Quinone Sesquiterpene Penicilliumin A |
title_fullStr | Myrothecols G and H, Two New Analogues of the Marine-Derived Quinone Sesquiterpene Penicilliumin A |
title_full_unstemmed | Myrothecols G and H, Two New Analogues of the Marine-Derived Quinone Sesquiterpene Penicilliumin A |
title_short | Myrothecols G and H, Two New Analogues of the Marine-Derived Quinone Sesquiterpene Penicilliumin A |
title_sort | myrothecols g and h, two new analogues of the marine-derived quinone sesquiterpene penicilliumin a |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4483633/ https://www.ncbi.nlm.nih.gov/pubmed/26023841 http://dx.doi.org/10.3390/md13063360 |
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