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作 者:Dong-Mei Zhang Li-Li Wang Jia Li Li-Hong Hu
机构地区:[1]Shanghai Research Center for Modernization of Traditional Chinese Medicine, Shanghai Institute of Materia Medica, Shanghai Institute for Biological Sciences, the Chinese Academy of Sciences, Shanghai 201203, China [2]National Center for Drug Screening, Shanghai Institute of Materia Medica, Shanghai Institutes for Biological Sciences, the Chinese Academy of Sciences, Shanghai 201203, China [3]School of Pharmacy, East China University of Science and Technology, Shanghai 200237, China
出 处:《Journal of Integrative Plant Biology》2007年第2期218-221,共4页植物学报(英文版)
基 金:Supported by the National Natural Science Foundation of China (30371679).
摘 要:The ethanol extract of the stem bark of Fraxinus chinensis Roxb. showed good inhibitory bioactivity against VEGF receptor-1 kinase (IC50:13.8 μg/mL). In order to find new and bioactive compounds, the chemical constituents of the stem bark of F. chinensis were investigated and two new coumarins, namely 6'-O-sinapinoyl esculin (compound 1) and 6'-O-vanillyl esculin (compound 2), together with eleven known compounds (compounds 3-13) were isolated. The structures of the two new compounds were identified by their physicochemical properties and spectral analysis, particularly one- and two-dimensional nuclear magnetic resonance spectral methods. The known compound, oleuropein (compound 11), exhibited moderate activity (IC50:(8.7 ± 1.3) μmol/L) to inhibit VEGF receptor- 1 kinase.The ethanol extract of the stem bark of Fraxinus chinensis Roxb. showed good inhibitory bioactivity against VEGF receptor-1 kinase (IC50:13.8 μg/mL). In order to find new and bioactive compounds, the chemical constituents of the stem bark of F. chinensis were investigated and two new coumarins, namely 6'-O-sinapinoyl esculin (compound 1) and 6'-O-vanillyl esculin (compound 2), together with eleven known compounds (compounds 3-13) were isolated. The structures of the two new compounds were identified by their physicochemical properties and spectral analysis, particularly one- and two-dimensional nuclear magnetic resonance spectral methods. The known compound, oleuropein (compound 11), exhibited moderate activity (IC50:(8.7 ± 1.3) μmol/L) to inhibit VEGF receptor- 1 kinase.
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