Cargando…

Ypsiyunnosides A–E, Five New Cholestanol Glycosides from Ypsilandrayunnanensis

ABSTRACT: Phytochemical investigation on the whole plants of Ypsilandra yunnanensis was carried out for the first time and led to the isolation of five new cholestanol glycosides, ypsiyunnosides A–E (1–5), and one known analogue. Their structures were determined mainly by detailed spectroscopic anal...

Descripción completa

Detalles Bibliográficos
Autores principales: Chen, Yu, Si, Yong-Ai, Ni, Wei, Yan, Huan, Qin, Xu-Jie, Chen, Chang-Xiang, Liu, Hai-Yang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5385661/
https://www.ncbi.nlm.nih.gov/pubmed/27095014
http://dx.doi.org/10.1007/s13659-016-0098-2
_version_ 1782520637810540544
author Chen, Yu
Si, Yong-Ai
Ni, Wei
Yan, Huan
Qin, Xu-Jie
Chen, Chang-Xiang
Liu, Hai-Yang
author_facet Chen, Yu
Si, Yong-Ai
Ni, Wei
Yan, Huan
Qin, Xu-Jie
Chen, Chang-Xiang
Liu, Hai-Yang
author_sort Chen, Yu
collection PubMed
description ABSTRACT: Phytochemical investigation on the whole plants of Ypsilandra yunnanensis was carried out for the first time and led to the isolation of five new cholestanol glycosides, ypsiyunnosides A–E (1–5), and one known analogue. Their structures were determined mainly by detailed spectroscopic analysis, including extensive 1D and 2D NMR, MS and UV, as well as chemical methods. Among them, compound 1 possessed a rare 6/6/6/5/5 fused-rings cholestanol sketelon, which was identified as (23R,25R)-3β,16α,26-triol-16,23-cyclocholest-5,17(20)-dien-22-one. Their induced platelet aggregation activities and cytotoxicities were evaluated. GRAPHICAL ABSTRACT: Five new cholestanol glycosides, ypsiyunnosides A–E (1–5), were isolated from the whole plants of Ypsilandra yunnanensis. Compound 1 possessed a rare 6/6/6/5/5 fused-rings cholestanol sketelon. Their structures were elucidated by a combination of 1D and 2D NMR, MS and chemical analysis. [Image: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s13659-016-0098-2) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-5385661
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Springer Berlin Heidelberg
record_format MEDLINE/PubMed
spelling pubmed-53856612017-04-24 Ypsiyunnosides A–E, Five New Cholestanol Glycosides from Ypsilandrayunnanensis Chen, Yu Si, Yong-Ai Ni, Wei Yan, Huan Qin, Xu-Jie Chen, Chang-Xiang Liu, Hai-Yang Nat Prod Bioprospect Original Article ABSTRACT: Phytochemical investigation on the whole plants of Ypsilandra yunnanensis was carried out for the first time and led to the isolation of five new cholestanol glycosides, ypsiyunnosides A–E (1–5), and one known analogue. Their structures were determined mainly by detailed spectroscopic analysis, including extensive 1D and 2D NMR, MS and UV, as well as chemical methods. Among them, compound 1 possessed a rare 6/6/6/5/5 fused-rings cholestanol sketelon, which was identified as (23R,25R)-3β,16α,26-triol-16,23-cyclocholest-5,17(20)-dien-22-one. Their induced platelet aggregation activities and cytotoxicities were evaluated. GRAPHICAL ABSTRACT: Five new cholestanol glycosides, ypsiyunnosides A–E (1–5), were isolated from the whole plants of Ypsilandra yunnanensis. Compound 1 possessed a rare 6/6/6/5/5 fused-rings cholestanol sketelon. Their structures were elucidated by a combination of 1D and 2D NMR, MS and chemical analysis. [Image: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s13659-016-0098-2) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2016-04-20 /pmc/articles/PMC5385661/ /pubmed/27095014 http://dx.doi.org/10.1007/s13659-016-0098-2 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Article
Chen, Yu
Si, Yong-Ai
Ni, Wei
Yan, Huan
Qin, Xu-Jie
Chen, Chang-Xiang
Liu, Hai-Yang
Ypsiyunnosides A–E, Five New Cholestanol Glycosides from Ypsilandrayunnanensis
title Ypsiyunnosides A–E, Five New Cholestanol Glycosides from Ypsilandrayunnanensis
title_full Ypsiyunnosides A–E, Five New Cholestanol Glycosides from Ypsilandrayunnanensis
title_fullStr Ypsiyunnosides A–E, Five New Cholestanol Glycosides from Ypsilandrayunnanensis
title_full_unstemmed Ypsiyunnosides A–E, Five New Cholestanol Glycosides from Ypsilandrayunnanensis
title_short Ypsiyunnosides A–E, Five New Cholestanol Glycosides from Ypsilandrayunnanensis
title_sort ypsiyunnosides a–e, five new cholestanol glycosides from ypsilandrayunnanensis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5385661/
https://www.ncbi.nlm.nih.gov/pubmed/27095014
http://dx.doi.org/10.1007/s13659-016-0098-2
work_keys_str_mv AT chenyu ypsiyunnosidesaefivenewcholestanolglycosidesfromypsilandrayunnanensis
AT siyongai ypsiyunnosidesaefivenewcholestanolglycosidesfromypsilandrayunnanensis
AT niwei ypsiyunnosidesaefivenewcholestanolglycosidesfromypsilandrayunnanensis
AT yanhuan ypsiyunnosidesaefivenewcholestanolglycosidesfromypsilandrayunnanensis
AT qinxujie ypsiyunnosidesaefivenewcholestanolglycosidesfromypsilandrayunnanensis
AT chenchangxiang ypsiyunnosidesaefivenewcholestanolglycosidesfromypsilandrayunnanensis
AT liuhaiyang ypsiyunnosidesaefivenewcholestanolglycosidesfromypsilandrayunnanensis