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A Sterol and Spiroditerpenoids from a Penicillium sp. Isolated from a Deep Sea Sediment Sample

A new polyoxygenated sterol, sterolic acid (1), three new breviane spiroditerpenoids, breviones I–K (2–4), and the known breviones (5–8), were isolated from the crude extract of a Penicillium sp. obtained from a deep sea sediment sample that was collected at a depth of 5115 m. The structures of 1–4...

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Detalles Bibliográficos
Autores principales: Li, Yan, Ye, Dezan, Shao, Zongze, Cui, Chengbin, Che, Yongsheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3297011/
https://www.ncbi.nlm.nih.gov/pubmed/22412815
http://dx.doi.org/10.3390/md10020497
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author Li, Yan
Ye, Dezan
Shao, Zongze
Cui, Chengbin
Che, Yongsheng
author_facet Li, Yan
Ye, Dezan
Shao, Zongze
Cui, Chengbin
Che, Yongsheng
author_sort Li, Yan
collection PubMed
description A new polyoxygenated sterol, sterolic acid (1), three new breviane spiroditerpenoids, breviones I–K (2–4), and the known breviones (5–8), were isolated from the crude extract of a Penicillium sp. obtained from a deep sea sediment sample that was collected at a depth of 5115 m. The structures of 1–4 were elucidated primarily by NMR experiments, and 1 was further confirmed by X-ray crystallography. The absolute configurations of 2 and 3 were deduced by comparison of their CD spectra with those of the model compounds. Compounds 2 and 5 showed significant cytotoxicity against MCF-7 cells, which is comparable to the positive control cisplatin.
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spelling pubmed-32970112012-03-12 A Sterol and Spiroditerpenoids from a Penicillium sp. Isolated from a Deep Sea Sediment Sample Li, Yan Ye, Dezan Shao, Zongze Cui, Chengbin Che, Yongsheng Mar Drugs Article A new polyoxygenated sterol, sterolic acid (1), three new breviane spiroditerpenoids, breviones I–K (2–4), and the known breviones (5–8), were isolated from the crude extract of a Penicillium sp. obtained from a deep sea sediment sample that was collected at a depth of 5115 m. The structures of 1–4 were elucidated primarily by NMR experiments, and 1 was further confirmed by X-ray crystallography. The absolute configurations of 2 and 3 were deduced by comparison of their CD spectra with those of the model compounds. Compounds 2 and 5 showed significant cytotoxicity against MCF-7 cells, which is comparable to the positive control cisplatin. MDPI 2012-02-20 /pmc/articles/PMC3297011/ /pubmed/22412815 http://dx.doi.org/10.3390/md10020497 Text en © 2012 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ 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
Li, Yan
Ye, Dezan
Shao, Zongze
Cui, Chengbin
Che, Yongsheng
A Sterol and Spiroditerpenoids from a Penicillium sp. Isolated from a Deep Sea Sediment Sample
title A Sterol and Spiroditerpenoids from a Penicillium sp. Isolated from a Deep Sea Sediment Sample
title_full A Sterol and Spiroditerpenoids from a Penicillium sp. Isolated from a Deep Sea Sediment Sample
title_fullStr A Sterol and Spiroditerpenoids from a Penicillium sp. Isolated from a Deep Sea Sediment Sample
title_full_unstemmed A Sterol and Spiroditerpenoids from a Penicillium sp. Isolated from a Deep Sea Sediment Sample
title_short A Sterol and Spiroditerpenoids from a Penicillium sp. Isolated from a Deep Sea Sediment Sample
title_sort sterol and spiroditerpenoids from a penicillium sp. isolated from a deep sea sediment sample
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3297011/
https://www.ncbi.nlm.nih.gov/pubmed/22412815
http://dx.doi.org/10.3390/md10020497
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