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Steroidal and pregnane glycosides from Ypsilandra thibetica

The whole plants of Ypsilandra thibetica have been analyzed as part of a systematic study on saponin constituents of medicinal plants. This has resulted in the isolation of two new bisdesmosidic furostanol saponins, named ypsilandroside P (1) and ypsilandroside Q (2), and one new pregnane glycoside,...

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Autores principales: Liu, Hai-Yang, Chen, Chang-Xiang, Lu, Yi, Yang, Jun-Yun, Ni, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4131569/
http://dx.doi.org/10.1007/s13659-011-0039-z
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author Liu, Hai-Yang
Chen, Chang-Xiang
Lu, Yi
Yang, Jun-Yun
Ni, Wei
author_facet Liu, Hai-Yang
Chen, Chang-Xiang
Lu, Yi
Yang, Jun-Yun
Ni, Wei
author_sort Liu, Hai-Yang
collection PubMed
description The whole plants of Ypsilandra thibetica have been analyzed as part of a systematic study on saponin constituents of medicinal plants. This has resulted in the isolation of two new bisdesmosidic furostanol saponins, named ypsilandroside P (1) and ypsilandroside Q (2), and one new pregnane glycoside, named ypsilandroside R (3), together with nine known steroidal glycosides. Their structures were elucidated on the basis of extensive spectroscopic analysis, including that of 2D NMR data, and the results of acidic hydrolysis. Ypsilandroside P (1) was cytotoxicity against two human tumor cell lines. [Image: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: Supplementary material is available for this article at 10.1007/s13659-011-0039-z and is accessible for authorized users.
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spelling pubmed-41315692014-08-20 Steroidal and pregnane glycosides from Ypsilandra thibetica Liu, Hai-Yang Chen, Chang-Xiang Lu, Yi Yang, Jun-Yun Ni, Wei Nat Prod Bioprospect Regular Article The whole plants of Ypsilandra thibetica have been analyzed as part of a systematic study on saponin constituents of medicinal plants. This has resulted in the isolation of two new bisdesmosidic furostanol saponins, named ypsilandroside P (1) and ypsilandroside Q (2), and one new pregnane glycoside, named ypsilandroside R (3), together with nine known steroidal glycosides. Their structures were elucidated on the basis of extensive spectroscopic analysis, including that of 2D NMR data, and the results of acidic hydrolysis. Ypsilandroside P (1) was cytotoxicity against two human tumor cell lines. [Image: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: Supplementary material is available for this article at 10.1007/s13659-011-0039-z and is accessible for authorized users. Springer Berlin Heidelberg 2012-01-14 /pmc/articles/PMC4131569/ http://dx.doi.org/10.1007/s13659-011-0039-z 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
Liu, Hai-Yang
Chen, Chang-Xiang
Lu, Yi
Yang, Jun-Yun
Ni, Wei
Steroidal and pregnane glycosides from Ypsilandra thibetica
title Steroidal and pregnane glycosides from Ypsilandra thibetica
title_full Steroidal and pregnane glycosides from Ypsilandra thibetica
title_fullStr Steroidal and pregnane glycosides from Ypsilandra thibetica
title_full_unstemmed Steroidal and pregnane glycosides from Ypsilandra thibetica
title_short Steroidal and pregnane glycosides from Ypsilandra thibetica
title_sort steroidal and pregnane glycosides from ypsilandra thibetica
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4131569/
http://dx.doi.org/10.1007/s13659-011-0039-z
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