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作 者:姚雯[1] 孙培环[1] 徐晓敏[1] 李雅娟[1] 袁呈山[2] 王振华[1,3]
机构地区:[1]石河子大学药学院/新疆特种植物药资源教育部重点实验室,新疆石河子832002 [2]兰州大学功能有机分子化学国家重点实验室,兰州730000 [3]烟台大学生命科学学院,山东烟台264005
出 处:《中国实验方剂学杂志》2014年第22期95-99,共5页Chinese Journal of Experimental Traditional Medical Formulae
基 金:国家自然科学基金项目(11175222);教育部新世纪优秀人才支持计划(NCET-10-0967)
摘 要:目的:研究苦豆子种子的化学成分并对其抗肿瘤活性进行测试。方法:采用常规的硅胶柱层析(CC),葡聚糖(Sephadex LH-20)柱层析,和重结晶等实验手段对其进行了分离纯化,利用波谱技术(1H-NMR,13C-NMR)及与文献数据对照,对分离的化合物进行了结构鉴定;并采用MTT测定部分生物碱单体化合物体外对C6肿瘤细胞的细胞毒活性。结果:共分离出7个生物碱类化合物,分别鉴定为:苦参碱(1),氧化苦参碱(2),槐果碱(3),9α-羟基槐果碱(4),氧化槐果碱(5),9α-羟基槐胺碱(6),(-)-13,14-去氢槐定碱(7),1个非生物碱化合物3-吲哚甲醛(8)。结论:化合物8为首次从该属植物中分离得到。细胞毒活性测试结果表明,化合物1-3和5对鼠脑胶质瘤C6细胞显示了较强的生长抑制活性。Objective: To investigate the chemical constituents in seed of Sophora alopecuroides and to determine their antitumor activities in vitro. Method: Compounds were isolated and purified by means of silica gel and Sephadex LH-20 gel columm chromatography,and recrystallization etc. Their structures were elucidated using spectroscopic analysis including1H-NMR,13C-NMR and spectral data. The cytotoxic activities of the alkaloids compounds on C6 cell in vitro were evaluated by MTT method. Result: Seven compounds were isolated from the ethanol extract of the seed of S. alopecuroides. Their structrues were identified as( +)-matrine( 1),( +)-oxymatrine( 2),(-)-sophocarpine( 3),(-)-9α-hydroxysophocarpine( 4),( +)-oxysophocarpine( 5),(-)-9α-hydroxysophoramine( 6),(-)-13,14-dehydrosophoridine( 7),and a non-alkaloid named indolyl-3-carbaldehyde( 8). Conclusion: The compond 8 was isolated from the genus sophora for the first time.Compounds 1-3 and 5 showed significant inhibitory activity towards C6 glioma cells.
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