Four new labdane-type diterpenoid glycosides from Diplopterygium laevissimum

Four new labdane-type diterpenoid glycosides, laevissiosides A-D (1–4) were isolated from the 95% ethanol extract of Diplopterygium laevissimum (Christ) Nakai, along with two known analogues, 18- β-D-glucopyranosyl ester-sclareol (5) and 18-hydroxy-sclareol (6). The structures of compounds 1–4 were...

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Detalles Bibliográficos
Autores principales: Li, Ming-Ming, Wang, Kou, He, Juan, Peng, Li-Yan, Chen, Xuan-Qin, Cheng, Xiao, Zhao, Qin-Shi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2013
Materias:
Regular Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4131659/
http://dx.doi.org/10.1007/s13659-012-0022-3
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author Li, Ming-Ming
Wang, Kou
He, Juan
Peng, Li-Yan
Chen, Xuan-Qin
Cheng, Xiao
Zhao, Qin-Shi
author_facet Li, Ming-Ming
Wang, Kou
He, Juan
Peng, Li-Yan
Chen, Xuan-Qin
Cheng, Xiao
Zhao, Qin-Shi
author_sort Li, Ming-Ming
collection PubMed
description Four new labdane-type diterpenoid glycosides, laevissiosides A-D (1–4) were isolated from the 95% ethanol extract of Diplopterygium laevissimum (Christ) Nakai, along with two known analogues, 18- β-D-glucopyranosyl ester-sclareol (5) and 18-hydroxy-sclareol (6). The structures of compounds 1–4 were elucidated by extensive 1D and 2D NMR spectroscopy as well as high-resolution MS analyses. All isolated compounds were evaluated for their cytotoxic effects. [Image: see text]
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spelling pubmed-41316592014-08-20 Four new labdane-type diterpenoid glycosides from Diplopterygium laevissimum Li, Ming-Ming Wang, Kou He, Juan Peng, Li-Yan Chen, Xuan-Qin Cheng, Xiao Zhao, Qin-Shi Nat Prod Bioprospect Regular Article Four new labdane-type diterpenoid glycosides, laevissiosides A-D (1–4) were isolated from the 95% ethanol extract of Diplopterygium laevissimum (Christ) Nakai, along with two known analogues, 18- β-D-glucopyranosyl ester-sclareol (5) and 18-hydroxy-sclareol (6). The structures of compounds 1–4 were elucidated by extensive 1D and 2D NMR spectroscopy as well as high-resolution MS analyses. All isolated compounds were evaluated for their cytotoxic effects. [Image: see text] Springer Berlin Heidelberg 2013-03-02 /pmc/articles/PMC4131659/ http://dx.doi.org/10.1007/s13659-012-0022-3 Text en © The Author(s) 2012 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
Li, Ming-Ming
Wang, Kou
He, Juan
Peng, Li-Yan
Chen, Xuan-Qin
Cheng, Xiao
Zhao, Qin-Shi
Four new labdane-type diterpenoid glycosides from Diplopterygium laevissimum
title Four new labdane-type diterpenoid glycosides from Diplopterygium laevissimum
title_full Four new labdane-type diterpenoid glycosides from Diplopterygium laevissimum
title_fullStr Four new labdane-type diterpenoid glycosides from Diplopterygium laevissimum
title_full_unstemmed Four new labdane-type diterpenoid glycosides from Diplopterygium laevissimum
title_short Four new labdane-type diterpenoid glycosides from Diplopterygium laevissimum
title_sort four new labdane-type diterpenoid glycosides from diplopterygium laevissimum
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4131659/
http://dx.doi.org/10.1007/s13659-012-0022-3
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