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作 者:顾青[1] 蔡银娜 杨光明[1,2] 蔡宝昌[1,2] 潘扬
机构地区:[1]南京中医药大学江苏省中药炮制重点实验室,南京210023 [2]国家中医药管理局中药炮制标准重点实验室,南京210023
出 处:《中国实验方剂学杂志》2013年第11期72-75,共4页Chinese Journal of Experimental Traditional Medical Formulae
基 金:国家自然科学基金项目(30902012);江苏省中医药局项目(LB09026)
摘 要:目的:研究藏药镰形棘豆Oxytropis falcata的化学组成及其抗肿瘤活性。方法:通过硅胶柱色谱、制备TLC分离纯化镰形棘豆的化学成分,通过NMR等波谱技术解析鉴定化合物结构,通过MTT法研究化合物1,3,5抑制人肝癌细胞HepG2、小鼠黑色素瘤细胞B16F10、人肝癌细胞SMMC-7721、人肝癌细胞HuH7以及人乳腺癌细胞MDA-MB-231的增殖影响。结果:从镰形棘豆乙醇提取物中分离得到了5个化合物,分别为7-甲氧基二氢黄酮(7-methoxy flavanone,1),7-羟基二氢黄酮(7-hydroxy flavonone,2),2',4'-二羟基査耳酮(2',4'-dihydroxy chalcone,3),2',4'-二羟基-4'-甲氧基查尔酮(2',4'-dihydroxy-4'-methoxy chalcone,4),N-(2-苯乙基)肉桂酰胺(N-2-phenylethyl cinnamamide,5)。四甲基偶氮唑盐比色(MTT)结果表明化合物3具有较好的抗肿瘤活性,其IC50分别为68.60,169.67,105.88,175.18,172.37μmol.L-1。结论:其中化合物5为首次从该种属中分离得到,化合物3对5种肿瘤细胞的增殖具有明显的抑制作用。Objective: To study the constituents from Oxytropis falcate and their antitumor activity. Method: Constituent isolation and purification was carried by column chromatography and their structures were elucidated on the basis of spectral data analysis.Cytotoxicity of compounds 1, 3, 5 was assessed using MTT colorimetric method against HepG2, B16F10, SMMC-7721, HuH7 and MDA-MB-231 tumor cell lines. Result: Five compounds(1-5) were elucidated as 7-methoxy flavanone (1), 7-hydroxy flavonone (2), 2', 4'-dihydroxy chalcone (3), 2', 4'-dihydroxy-4'-methoxy chalcone (4) and N-2-phenylethylcinnamamide (5). The compounds 3 showed the strongest cytotoxic effect on these five cell lines with IC50 values of 68.60, 169.67, 105.88, 175.18, 172.37 μmol·L^-1respectively. Conclusion: Compound 5 was isolated from this genus for the first time. Compound 3 showed significant antitumor activity.
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