Preparative Separation of Phenolic Compounds from Halimodendron halodendron by High-Speed Counter-Current Chromatography 英文参考文献.docVIP

Preparative Separation of Phenolic Compounds from Halimodendron halodendron by High-Speed Counter-Current Chromatography 英文参考文献.doc

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Preparative Separation of Phenolic Compounds from Halimodendron halodendron by High-Speed Counter-Current Chromatography 英文参考文献

Molecules 2010, 15, 5998-6007; doi:10.3390/moleculeOPEN ACCESS molecules ISSN 1420-3049 /journal/molecules Article Preparative Separation of Phenolic Compounds from Halimodendron halodendron by High-Speed Counter-Current Chromatography Jihua Wang 1, Haifeng Gao 1, Jianglin Zhao 1, Qi Wang 1, Ligang Zhou 1,*, Jianguo Han 2, Zhu Yu 2 and Fuyu Yang 2 1 College of Agronomy and Biotechnology, China Agricultural University, Beijing 100193, China 2 College of Animal Science and Technology, China Agricultural University, Beijing 100193, China * Author to whom correspondence should be addressed; E-Mail: lgzhou@; Tel.: +86 10 Received: 30 July 2010; in revised form: 16 August 2010 / Accepted: 27 August 2010 / Published: 31 August 2010 Abstract: Three phenolic compounds, p-hydroxybenzoic acid (1), isorhamnetin-3-O-β-D- rutinoside (2), and 3,3-di-O-methylquercetin (5), along with a phenolic mixture were successfully separated from the ethyl acetate crude extract of Halimodendron halodendron by high-speed counter-current chromatography (HSCCC) with chloroform-methanol- water-acetic acid (4:3:2:0.05, v/v) as the two-phase solvent system. The phenolic mixture from HSCCC was further separated by preparative HPLC and purified by Sephadex LH-20 to afford quercetin (3) and 3-O-methylquercetin (4). Seven hundred mg of ethyl acetate crude extract was separated by HSCCC to obtain six fractions which were then analyzed by high performance liquid chromatography (HPLC). The HSCCC separation obtained total of 80 mg of the mixture of quercetin (3) and 3-O-methylquercetin (4) (26.43% and 71.89%, respectively) in fraction 2, 14 mg of 3,3-di-O-methylquercetin (5) at 95.14% of purity in fraction 3, 15 mg of p-hydroxybenzoic acid (1) at 92.83% of purity in fraction 5, 12 mg of isorhamnetin-3-O-β-D-rutinoside (2) at 97.99% of purity in fraction 6. This is the first time these phenolic compounds have been o

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