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Preparative Isolation of Three Anthraquinones from Rumex japonicus by High-Speed Counter-Current Chromatography

Three anthraquinones—emodin, chrysophanol, and physcion—were successfully purified from the dichloromethane extract of the Chinese medicinal herb Rumex japonicus by high-speed counter-current chromatography (HSCCC). The extract was separated with n-hexane–ethanol–water (18:22:3, v/v/v) as the two-ph...

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Detalles Bibliográficos
Autores principales: Guo, Shuying, Feng, Bo, Zhu, Ruonan, Ma, Jiankang, Wang, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259845/
https://www.ncbi.nlm.nih.gov/pubmed/21273951
http://dx.doi.org/10.3390/molecules16021201
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author Guo, Shuying
Feng, Bo
Zhu, Ruonan
Ma, Jiankang
Wang, Wei
author_facet Guo, Shuying
Feng, Bo
Zhu, Ruonan
Ma, Jiankang
Wang, Wei
author_sort Guo, Shuying
collection PubMed
description Three anthraquinones—emodin, chrysophanol, and physcion—were successfully purified from the dichloromethane extract of the Chinese medicinal herb Rumex japonicus by high-speed counter-current chromatography (HSCCC). The extract was separated with n-hexane–ethanol–water (18:22:3, v/v/v) as the two-phase solvent system and yielded 3.4 mg of emodin, 24.1 mg of chrysophanol, and 2.0 mg of physcion from 500 mg of sample with purities of 99.2 %, 98.8% and 98.2%, respectively. The HSCCC fractions were analyzed by high-performance liquid chromatography (HPLC) and the chemical structures of the three anthraquinones were confirmed by (1)H-NMR and (13)C-NMR analysis. This is the first time these anthraquinones have been obtained from R. japonicus by HSCCC.
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spelling pubmed-62598452018-12-20 Preparative Isolation of Three Anthraquinones from Rumex japonicus by High-Speed Counter-Current Chromatography Guo, Shuying Feng, Bo Zhu, Ruonan Ma, Jiankang Wang, Wei Molecules Article Three anthraquinones—emodin, chrysophanol, and physcion—were successfully purified from the dichloromethane extract of the Chinese medicinal herb Rumex japonicus by high-speed counter-current chromatography (HSCCC). The extract was separated with n-hexane–ethanol–water (18:22:3, v/v/v) as the two-phase solvent system and yielded 3.4 mg of emodin, 24.1 mg of chrysophanol, and 2.0 mg of physcion from 500 mg of sample with purities of 99.2 %, 98.8% and 98.2%, respectively. The HSCCC fractions were analyzed by high-performance liquid chromatography (HPLC) and the chemical structures of the three anthraquinones were confirmed by (1)H-NMR and (13)C-NMR analysis. This is the first time these anthraquinones have been obtained from R. japonicus by HSCCC. MDPI 2011-01-27 /pmc/articles/PMC6259845/ /pubmed/21273951 http://dx.doi.org/10.3390/molecules16021201 Text en © 2011 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 license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Guo, Shuying
Feng, Bo
Zhu, Ruonan
Ma, Jiankang
Wang, Wei
Preparative Isolation of Three Anthraquinones from Rumex japonicus by High-Speed Counter-Current Chromatography
title Preparative Isolation of Three Anthraquinones from Rumex japonicus by High-Speed Counter-Current Chromatography
title_full Preparative Isolation of Three Anthraquinones from Rumex japonicus by High-Speed Counter-Current Chromatography
title_fullStr Preparative Isolation of Three Anthraquinones from Rumex japonicus by High-Speed Counter-Current Chromatography
title_full_unstemmed Preparative Isolation of Three Anthraquinones from Rumex japonicus by High-Speed Counter-Current Chromatography
title_short Preparative Isolation of Three Anthraquinones from Rumex japonicus by High-Speed Counter-Current Chromatography
title_sort preparative isolation of three anthraquinones from rumex japonicus by high-speed counter-current chromatography
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259845/
https://www.ncbi.nlm.nih.gov/pubmed/21273951
http://dx.doi.org/10.3390/molecules16021201
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