5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one

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CAS: 480-10-4
MF: C21H20O11
MW: 448.3769
Synonyms: 5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one

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Du-Jin Wang

Institute of Chemistry, Chinese Academy of Sciences
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Xin Lu

Chinese Academy of Sciences
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Jing Wang

Nankai Univerisity
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Wei Liu

The University of Science and Technology of China
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Wei Zhang

Shanghai Jiaotong University
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Yun Wei

Beijing University of Chemical Technology
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Co-reporter: Qianqian Xie, Yun Wei, Guoliang Zhang
pp: 229-233
Publication Date(Web):20 April 2010
DOI: 10.1016/j.seppur.2010.02.012
In order to utilize and control the invasive weed, Flaveria bidentis (L.) Kuntze, bioactive compounds mainly flavonoids from F. bidentis (L.) Kuntze were studied. High-speed counter-current chromatography (HSCCC) was successfully used for the separation of flavonol glycosides from F. bidentis (L.) Kuntze. The two-phase solvent system composed of ethyl acetate–methanol–water (10:0.4:10, v/v) was used for HSCCC. About 400 mg of the crude extract was separated by HSCCC, yielding 3.6 mg of patuletin-3-O-glucoside at a purity of over 97%; 4.4 mg of astragalin (kaempferol-3-O-glucoside) at a purity of over 98% and 4.5 mg of a mixture of hyperoside (quercetin-3-O-galactoside) and 6-methoxykaempferol-3-O-galactoside constituting over 97% of the fraction. The chemical structures were confirmed by MS and 1H, 13C, 1-D TOCSY NMR.

Xiao-Qing Chen

Central South University
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Hua Yang

Central South University
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Qiang Liu

Hunan University
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Jing Li

China Agricultural University
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