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Isolation of farnesylhydroquinones from the basidiomycete Ganoderma pfeifferi

Two farnesylhydroquinones were isolated from the fruiting bodies of Ganoderma pfeifferi, farnesylhydroquinone (1) and the new compound ganomycin K (2), (5S)-3-[(E)-7,8-dihydroxy-4,8-dimethylnon-3-enyl]-5-(2,5-dihydroxyphenyl)-furan-2(5H)-one. The structures of 1 and 2 were determined on the basis of...

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Autores principales: Niedermeyer, Timo H. J., Jira, Thomas, Lalk, Michael, Lindequist, Ulrike
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4131579/
http://dx.doi.org/10.1007/s13659-013-0036-5
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author Niedermeyer, Timo H. J.
Jira, Thomas
Lalk, Michael
Lindequist, Ulrike
author_facet Niedermeyer, Timo H. J.
Jira, Thomas
Lalk, Michael
Lindequist, Ulrike
author_sort Niedermeyer, Timo H. J.
collection PubMed
description Two farnesylhydroquinones were isolated from the fruiting bodies of Ganoderma pfeifferi, farnesylhydroquinone (1) and the new compound ganomycin K (2), (5S)-3-[(E)-7,8-dihydroxy-4,8-dimethylnon-3-enyl]-5-(2,5-dihydroxyphenyl)-furan-2(5H)-one. The structures of 1 and 2 were determined on the basis of mass spectrometric and NMR spectroscopic evidence. The antibacterial activity of the isolated compounds was neglectable. [Image: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: Supplementary material is available for this article at 10.1007/s13659-013-0036-5 and is accessible for authorized users.
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spelling pubmed-41315792014-08-20 Isolation of farnesylhydroquinones from the basidiomycete Ganoderma pfeifferi Niedermeyer, Timo H. J. Jira, Thomas Lalk, Michael Lindequist, Ulrike Nat Prod Bioprospect Regular Article Two farnesylhydroquinones were isolated from the fruiting bodies of Ganoderma pfeifferi, farnesylhydroquinone (1) and the new compound ganomycin K (2), (5S)-3-[(E)-7,8-dihydroxy-4,8-dimethylnon-3-enyl]-5-(2,5-dihydroxyphenyl)-furan-2(5H)-one. The structures of 1 and 2 were determined on the basis of mass spectrometric and NMR spectroscopic evidence. The antibacterial activity of the isolated compounds was neglectable. [Image: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: Supplementary material is available for this article at 10.1007/s13659-013-0036-5 and is accessible for authorized users. Springer Berlin Heidelberg 2013-06-20 /pmc/articles/PMC4131579/ http://dx.doi.org/10.1007/s13659-013-0036-5 Text en © The Author(s) 2013 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
Niedermeyer, Timo H. J.
Jira, Thomas
Lalk, Michael
Lindequist, Ulrike
Isolation of farnesylhydroquinones from the basidiomycete Ganoderma pfeifferi
title Isolation of farnesylhydroquinones from the basidiomycete Ganoderma pfeifferi
title_full Isolation of farnesylhydroquinones from the basidiomycete Ganoderma pfeifferi
title_fullStr Isolation of farnesylhydroquinones from the basidiomycete Ganoderma pfeifferi
title_full_unstemmed Isolation of farnesylhydroquinones from the basidiomycete Ganoderma pfeifferi
title_short Isolation of farnesylhydroquinones from the basidiomycete Ganoderma pfeifferi
title_sort isolation of farnesylhydroquinones from the basidiomycete ganoderma pfeifferi
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4131579/
http://dx.doi.org/10.1007/s13659-013-0036-5
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