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棕树心化学成分研究
引用本文:桂利利,陈立,董俊兴.棕树心化学成分研究[J].军事医学,2017,41(1).
作者姓名:桂利利  陈立  董俊兴
作者单位:1. 安徽医科大学,合肥,230031;2. 军事医学科学院放射与辐射医学研究所,北京,100850;3. 安徽医科大学,合肥 230031; 军事医学科学院放射与辐射医学研究所,北京 100850
摘    要:目的:研究棕树心的化学成分。方法采用硅胶柱色谱、Sephadex LH-20凝胶柱色谱及重结晶等方法进行分离纯化,通过波谱数据分析和理化性质鉴别进行结构鉴定。结果从棕树心95%乙醇提取物中分离鉴定了10个化合物,分别鉴定为:1,3-二羟基蒽醌(1),大叶茜草素(2),4-羟基-2,6-二甲氧基-苯甲酸(3),5-羟基-2-羟甲基-γ-吡喃酮(4),3,5-二羟基-2-甲基-γ-吡喃酮(5),3,5-二羟基-γ-吡喃酮(6),胡萝卜苷(7),对羟基苯甲酸(8),儿茶酚(9),β-谷甾醇(10)。结论1~7为首次从该植物中分离得到,1~6为首次从棕榈属植物中分离得到。抗肿瘤体外活性筛选结果显示,化合物2对人骨肉瘤细胞株U20 S、人神经母细胞瘤细胞株SY5 Y均有一定的生长抑制作用,其IC50值分别为18.10、26.59μg/ml;化合物5对人乳腺癌细胞株MCF-7的生长有一定的抑制作用,其IC50值为37.31μg/ml。

关 键 词:棕榈  植物提取物  化学成分  结构鉴定  药物筛选试验  抗肿瘤

Chemical constituents from the heartwood of Trachycarpus fortunei (Hook.) H. Wendl
Authors:GUI Li-li  CHEN Li  DONG Jun-xing
Abstract:Objective To study the chemical constituents of the heartwood of Trachycarpus fortunei.Methods Compounds were isolated and purified by silica gel column , Sephadex LH-20 chromatography and recrystallization .Their structures were elucidated by physicochemical properties and spectral data .Results Ten compounds were isolated from the 95%ethanol extract of the heartwood of T.fortunei and identified as 1,3-dihydroxyanthraquinone (1),mollugin(2), 4-hydroxy-2, 6-dimethoxy-benzoic acid ( 3 ), 5-hydroxy-2-hydroxymethyl-γ-pyranone ( 4 ), 3, 5-dihydroxy-2-methyl-γ-pyranone(5),3,5-dihydroxy-γ-pyranone (6),daucosterol (7),4-hydroxybenzoic acid (8),pyrocatechol (9),β-sitosterol (10).Conclusion Compounds 1-7 have been obtained from this plant for the first time ,and 1-6 from the genus for the first time.The screening results of antitumor activity in vitro show that the half inhibitory concentration IC 50 of compound 2 for human osteosarcoma cells U20S and human neuroblastoma cells SY 5Y is 18.10 and 26.59 μg/ml respectively. Compound 5 can inhibit the growth of human breast cancer cells MCF-7 with a half inhibitory concentration IC 50 of 37.31μg/ml.
Keywords:Trachycarpus fortunei ( Hook  ) H  Wendl    plant extracts  chemical constituents  structural identification  drug screening assays  antitumor
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