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Cucurbitane triterpenoids from Hemsleya penxianensis

Two new cucurbitacins, jinfushanencins A (1) and B (2), seven new cucurbitane glycosides, jinfushanosides E-K (3–9), along with nine known analogues, were obtained from the tubers of Hemsleya penxianensis. Their structures were elucidated on the basis of extensive spectroscopic and chemical methods....

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Autores principales: Chen, Jian-Chao, Zhou, Lin, Wang, Yun-Hua, Tian, Ren-Rong, Yan, Yun-Xin, Nian, Yin, Sun, Yun, Zheng, Yong-Tang, Qiu, Ming-Hua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4131631/
http://dx.doi.org/10.1007/s13659-011-0044-2
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author Chen, Jian-Chao
Zhou, Lin
Wang, Yun-Hua
Tian, Ren-Rong
Yan, Yun-Xin
Nian, Yin
Sun, Yun
Zheng, Yong-Tang
Qiu, Ming-Hua
author_facet Chen, Jian-Chao
Zhou, Lin
Wang, Yun-Hua
Tian, Ren-Rong
Yan, Yun-Xin
Nian, Yin
Sun, Yun
Zheng, Yong-Tang
Qiu, Ming-Hua
author_sort Chen, Jian-Chao
collection PubMed
description Two new cucurbitacins, jinfushanencins A (1) and B (2), seven new cucurbitane glycosides, jinfushanosides E-K (3–9), along with nine known analogues, were obtained from the tubers of Hemsleya penxianensis. Their structures were elucidated on the basis of extensive spectroscopic and chemical methods. Selected isolates were tested their anti-HIV-1 activities, and compound 5 showed weak anti-HIV-1 in C8166 cell (EC(50) = 5.9 µg/mL) with a selectivity index of 13.5. [Image: see text]
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spelling pubmed-41316312014-08-20 Cucurbitane triterpenoids from Hemsleya penxianensis Chen, Jian-Chao Zhou, Lin Wang, Yun-Hua Tian, Ren-Rong Yan, Yun-Xin Nian, Yin Sun, Yun Zheng, Yong-Tang Qiu, Ming-Hua Nat Prod Bioprospect Regular Article Two new cucurbitacins, jinfushanencins A (1) and B (2), seven new cucurbitane glycosides, jinfushanosides E-K (3–9), along with nine known analogues, were obtained from the tubers of Hemsleya penxianensis. Their structures were elucidated on the basis of extensive spectroscopic and chemical methods. Selected isolates were tested their anti-HIV-1 activities, and compound 5 showed weak anti-HIV-1 in C8166 cell (EC(50) = 5.9 µg/mL) with a selectivity index of 13.5. [Image: see text] Springer Berlin Heidelberg 2012-05-24 /pmc/articles/PMC4131631/ http://dx.doi.org/10.1007/s13659-011-0044-2 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
Chen, Jian-Chao
Zhou, Lin
Wang, Yun-Hua
Tian, Ren-Rong
Yan, Yun-Xin
Nian, Yin
Sun, Yun
Zheng, Yong-Tang
Qiu, Ming-Hua
Cucurbitane triterpenoids from Hemsleya penxianensis
title Cucurbitane triterpenoids from Hemsleya penxianensis
title_full Cucurbitane triterpenoids from Hemsleya penxianensis
title_fullStr Cucurbitane triterpenoids from Hemsleya penxianensis
title_full_unstemmed Cucurbitane triterpenoids from Hemsleya penxianensis
title_short Cucurbitane triterpenoids from Hemsleya penxianensis
title_sort cucurbitane triterpenoids from hemsleya penxianensis
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4131631/
http://dx.doi.org/10.1007/s13659-011-0044-2
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