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Cytosporinols A-C, new caryophyllene sesquiterpenoids from Cytospora sp.
Three new caryophyllene sesquiterpenoids, cytosporinols A-C (1–3), have been isolated from solid cultures of Cytospora sp. The structures of 1–3 were elucidated primarily by NMR spectroscopy, and 3 was further confirmed by X-ray crystallography. The absolute configurations of the C-11 secondary alco...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4131587/ http://dx.doi.org/10.1007/s13659-012-0018-z |
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author | Li, Yan Li, Chang-Wei Cui, Cheng-Bin Liu, Xing-Zhong Che, Yong-Sheng |
author_facet | Li, Yan Li, Chang-Wei Cui, Cheng-Bin Liu, Xing-Zhong Che, Yong-Sheng |
author_sort | Li, Yan |
collection | PubMed |
description | Three new caryophyllene sesquiterpenoids, cytosporinols A-C (1–3), have been isolated from solid cultures of Cytospora sp. The structures of 1–3 were elucidated primarily by NMR spectroscopy, and 3 was further confirmed by X-ray crystallography. The absolute configurations of the C-11 secondary alcohol in 1 and the 6,8-diol moiety in 3 were deduced using the modified Mosher and Snatzke’s method, respectively. Compounds 2 and 3 showed moderate cytotoxicity against HeLa cells. [Image: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: Supplementary material is available for this article at 10.1007/s13659-012-0018-z and is accessible for authorized users. |
format | Online Article Text |
id | pubmed-4131587 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-41315872014-08-20 Cytosporinols A-C, new caryophyllene sesquiterpenoids from Cytospora sp. Li, Yan Li, Chang-Wei Cui, Cheng-Bin Liu, Xing-Zhong Che, Yong-Sheng Nat Prod Bioprospect Regular Article Three new caryophyllene sesquiterpenoids, cytosporinols A-C (1–3), have been isolated from solid cultures of Cytospora sp. The structures of 1–3 were elucidated primarily by NMR spectroscopy, and 3 was further confirmed by X-ray crystallography. The absolute configurations of the C-11 secondary alcohol in 1 and the 6,8-diol moiety in 3 were deduced using the modified Mosher and Snatzke’s method, respectively. Compounds 2 and 3 showed moderate cytotoxicity against HeLa cells. [Image: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: Supplementary material is available for this article at 10.1007/s13659-012-0018-z and is accessible for authorized users. Springer Berlin Heidelberg 2012-03-20 /pmc/articles/PMC4131587/ http://dx.doi.org/10.1007/s13659-012-0018-z Text en © The Author(s) 2012 |
spellingShingle | Regular Article Li, Yan Li, Chang-Wei Cui, Cheng-Bin Liu, Xing-Zhong Che, Yong-Sheng Cytosporinols A-C, new caryophyllene sesquiterpenoids from Cytospora sp. |
title | Cytosporinols A-C, new caryophyllene sesquiterpenoids from Cytospora sp. |
title_full | Cytosporinols A-C, new caryophyllene sesquiterpenoids from Cytospora sp. |
title_fullStr | Cytosporinols A-C, new caryophyllene sesquiterpenoids from Cytospora sp. |
title_full_unstemmed | Cytosporinols A-C, new caryophyllene sesquiterpenoids from Cytospora sp. |
title_short | Cytosporinols A-C, new caryophyllene sesquiterpenoids from Cytospora sp. |
title_sort | cytosporinols a-c, new caryophyllene sesquiterpenoids from cytospora sp. |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4131587/ http://dx.doi.org/10.1007/s13659-012-0018-z |
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