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Six New Coumarin Glycosides from the Aerial Parts of Gendarussa vulgaris

Six new coumarin glycosides, genglycoside A–F (1–6), were isolated from the aerial parts of Gendarussa vulgaris, along with ten known analogues (7–16). Their structures were unambiguously established on the basis of extensive spectroscopic data and HPLC analysis. The cytotoxic activities of all isol...

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Detalles Bibliográficos
Autores principales: Sun, Yanjun, Gao, Meiling, Chen, Haojie, Han, Ruijie, Chen, Hui, Du, Kun, Zhang, Yanli, Li, Meng, Si, Yingying, Feng, Weisheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6514664/
https://www.ncbi.nlm.nih.gov/pubmed/31013828
http://dx.doi.org/10.3390/molecules24081456
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author Sun, Yanjun
Gao, Meiling
Chen, Haojie
Han, Ruijie
Chen, Hui
Du, Kun
Zhang, Yanli
Li, Meng
Si, Yingying
Feng, Weisheng
author_facet Sun, Yanjun
Gao, Meiling
Chen, Haojie
Han, Ruijie
Chen, Hui
Du, Kun
Zhang, Yanli
Li, Meng
Si, Yingying
Feng, Weisheng
author_sort Sun, Yanjun
collection PubMed
description Six new coumarin glycosides, genglycoside A–F (1–6), were isolated from the aerial parts of Gendarussa vulgaris, along with ten known analogues (7–16). Their structures were unambiguously established on the basis of extensive spectroscopic data and HPLC analysis. The cytotoxic activities of all isolated compounds were evaluated by MTT assay. Compound 12 showed the most potent cytotoxicity in Eca-109, MCF-7, and HepG2 cell lines. By the preliminary structure–activity relationships, it was firstly discovered that the glycosylation or esterification at 7,8-dihydroxy or 7-hydroxy drastically reduced the cytotoxic activity of the parent coumarin.
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spelling pubmed-65146642019-05-30 Six New Coumarin Glycosides from the Aerial Parts of Gendarussa vulgaris Sun, Yanjun Gao, Meiling Chen, Haojie Han, Ruijie Chen, Hui Du, Kun Zhang, Yanli Li, Meng Si, Yingying Feng, Weisheng Molecules Article Six new coumarin glycosides, genglycoside A–F (1–6), were isolated from the aerial parts of Gendarussa vulgaris, along with ten known analogues (7–16). Their structures were unambiguously established on the basis of extensive spectroscopic data and HPLC analysis. The cytotoxic activities of all isolated compounds were evaluated by MTT assay. Compound 12 showed the most potent cytotoxicity in Eca-109, MCF-7, and HepG2 cell lines. By the preliminary structure–activity relationships, it was firstly discovered that the glycosylation or esterification at 7,8-dihydroxy or 7-hydroxy drastically reduced the cytotoxic activity of the parent coumarin. MDPI 2019-04-12 /pmc/articles/PMC6514664/ /pubmed/31013828 http://dx.doi.org/10.3390/molecules24081456 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Sun, Yanjun
Gao, Meiling
Chen, Haojie
Han, Ruijie
Chen, Hui
Du, Kun
Zhang, Yanli
Li, Meng
Si, Yingying
Feng, Weisheng
Six New Coumarin Glycosides from the Aerial Parts of Gendarussa vulgaris
title Six New Coumarin Glycosides from the Aerial Parts of Gendarussa vulgaris
title_full Six New Coumarin Glycosides from the Aerial Parts of Gendarussa vulgaris
title_fullStr Six New Coumarin Glycosides from the Aerial Parts of Gendarussa vulgaris
title_full_unstemmed Six New Coumarin Glycosides from the Aerial Parts of Gendarussa vulgaris
title_short Six New Coumarin Glycosides from the Aerial Parts of Gendarussa vulgaris
title_sort six new coumarin glycosides from the aerial parts of gendarussa vulgaris
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6514664/
https://www.ncbi.nlm.nih.gov/pubmed/31013828
http://dx.doi.org/10.3390/molecules24081456
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