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A New Flavone C-Glycoside from Clematis rehderiana

A new flavone C-glycoside, isovitexin 6″-O-E-p-coumarate (1) and two known flavonoid glycosides—quercetin 3-O-β-D-glucuronopyranoside (2) and isoorientin (3)—were isolated from an ethanol extract of aerial parts of Clematis rehderiana. Their structures were determined by spectroscopic methods. The a...

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Detalles Bibliográficos
Autores principales: Du, Zhi-Zhi, Yang, Xian-Wen, Han, Hao, Cai, Xiang-Hai, Luo, Xiao-Dong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6263201/
https://www.ncbi.nlm.nih.gov/pubmed/20335937
http://dx.doi.org/10.3390/molecules15020672
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author Du, Zhi-Zhi
Yang, Xian-Wen
Han, Hao
Cai, Xiang-Hai
Luo, Xiao-Dong
author_facet Du, Zhi-Zhi
Yang, Xian-Wen
Han, Hao
Cai, Xiang-Hai
Luo, Xiao-Dong
author_sort Du, Zhi-Zhi
collection PubMed
description A new flavone C-glycoside, isovitexin 6″-O-E-p-coumarate (1) and two known flavonoid glycosides—quercetin 3-O-β-D-glucuronopyranoside (2) and isoorientin (3)—were isolated from an ethanol extract of aerial parts of Clematis rehderiana. Their structures were determined by spectroscopic methods. The antioxidant effects of the two flavone C-glycosides were evaluated by both the MTT and DPPH assays. Compound 1 showed potent activities against H(2)O(2)-induced impairment in PC12 cells within the concentration range tested, whereas compound 3 scavenged DPPH radical strongly, with an IC(50) value of 13.5 μM.
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spelling pubmed-62632012018-12-03 A New Flavone C-Glycoside from Clematis rehderiana Du, Zhi-Zhi Yang, Xian-Wen Han, Hao Cai, Xiang-Hai Luo, Xiao-Dong Molecules Communication A new flavone C-glycoside, isovitexin 6″-O-E-p-coumarate (1) and two known flavonoid glycosides—quercetin 3-O-β-D-glucuronopyranoside (2) and isoorientin (3)—were isolated from an ethanol extract of aerial parts of Clematis rehderiana. Their structures were determined by spectroscopic methods. The antioxidant effects of the two flavone C-glycosides were evaluated by both the MTT and DPPH assays. Compound 1 showed potent activities against H(2)O(2)-induced impairment in PC12 cells within the concentration range tested, whereas compound 3 scavenged DPPH radical strongly, with an IC(50) value of 13.5 μM. Molecular Diversity Preservation International 2010-01-29 /pmc/articles/PMC6263201/ /pubmed/20335937 http://dx.doi.org/10.3390/molecules15020672 Text en © 2010 by the authors; licensee Molecular Diversity Preservation International, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Communication
Du, Zhi-Zhi
Yang, Xian-Wen
Han, Hao
Cai, Xiang-Hai
Luo, Xiao-Dong
A New Flavone C-Glycoside from Clematis rehderiana
title A New Flavone C-Glycoside from Clematis rehderiana
title_full A New Flavone C-Glycoside from Clematis rehderiana
title_fullStr A New Flavone C-Glycoside from Clematis rehderiana
title_full_unstemmed A New Flavone C-Glycoside from Clematis rehderiana
title_short A New Flavone C-Glycoside from Clematis rehderiana
title_sort new flavone c-glycoside from clematis rehderiana
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6263201/
https://www.ncbi.nlm.nih.gov/pubmed/20335937
http://dx.doi.org/10.3390/molecules15020672
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