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Chemical investigation on the cultures of the fungus Xylaria carpophila

A chemical investigation on the cultures of Xylaria carpophila led to the isolation of one known cyclopeptide cyclo(Nmethyl-(l)-Phe-(l)-Pro-(l)-Leu-(d)-Ile-(l)-Val) (1), five new sesquiterpenes, named as xylcarpins A–E (2–6), and another known compound (7). The structures were determined by extensiv...

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Detalles Bibliográficos
Autores principales: Yin, Xia, Feng, Tao, Li, Zheng-Hui, Su, Jia, Li, Yan, Tan, Ning-Hua, Liu, Ji-Kai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4131652/
http://dx.doi.org/10.1007/s13659-011-0011-y
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author Yin, Xia
Feng, Tao
Li, Zheng-Hui
Su, Jia
Li, Yan
Tan, Ning-Hua
Liu, Ji-Kai
author_facet Yin, Xia
Feng, Tao
Li, Zheng-Hui
Su, Jia
Li, Yan
Tan, Ning-Hua
Liu, Ji-Kai
author_sort Yin, Xia
collection PubMed
description A chemical investigation on the cultures of Xylaria carpophila led to the isolation of one known cyclopeptide cyclo(Nmethyl-(l)-Phe-(l)-Pro-(l)-Leu-(d)-Ile-(l)-Val) (1), five new sesquiterpenes, named as xylcarpins A–E (2–6), and another known compound (7). The structures were determined by extensive NMR and MS spectroscopic analysis. The absolute configuration of 1 was established by use of Marfey’s method and ROESY spectroscopic data. All compounds were tested for their cytotoxicities against five human cancer cell lines. Compound 7 showed week inhibitory activity. [Image: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: Supplementary material is available for this article at 10.1007/s13659-011-0011-y and is accessible for authorized users.
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spelling pubmed-41316522014-08-20 Chemical investigation on the cultures of the fungus Xylaria carpophila Yin, Xia Feng, Tao Li, Zheng-Hui Su, Jia Li, Yan Tan, Ning-Hua Liu, Ji-Kai Nat Prod Bioprospect Regular Article A chemical investigation on the cultures of Xylaria carpophila led to the isolation of one known cyclopeptide cyclo(Nmethyl-(l)-Phe-(l)-Pro-(l)-Leu-(d)-Ile-(l)-Val) (1), five new sesquiterpenes, named as xylcarpins A–E (2–6), and another known compound (7). The structures were determined by extensive NMR and MS spectroscopic analysis. The absolute configuration of 1 was established by use of Marfey’s method and ROESY spectroscopic data. All compounds were tested for their cytotoxicities against five human cancer cell lines. Compound 7 showed week inhibitory activity. [Image: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: Supplementary material is available for this article at 10.1007/s13659-011-0011-y and is accessible for authorized users. Springer Berlin Heidelberg 2011-09-27 /pmc/articles/PMC4131652/ http://dx.doi.org/10.1007/s13659-011-0011-y Text en © The Author(s) 2011 https://creativecommons.org/licenses/by/4.0/ This article is published under license to BioMed Central Ltd. Open Access This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Regular Article
Yin, Xia
Feng, Tao
Li, Zheng-Hui
Su, Jia
Li, Yan
Tan, Ning-Hua
Liu, Ji-Kai
Chemical investigation on the cultures of the fungus Xylaria carpophila
title Chemical investigation on the cultures of the fungus Xylaria carpophila
title_full Chemical investigation on the cultures of the fungus Xylaria carpophila
title_fullStr Chemical investigation on the cultures of the fungus Xylaria carpophila
title_full_unstemmed Chemical investigation on the cultures of the fungus Xylaria carpophila
title_short Chemical investigation on the cultures of the fungus Xylaria carpophila
title_sort chemical investigation on the cultures of the fungus xylaria carpophila
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4131652/
http://dx.doi.org/10.1007/s13659-011-0011-y
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