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作 者:邹辉[1] 杨郴 易美玲[1] 吴富旋 盛习锋[1] 冯星[1]
出 处:《中国实验方剂学杂志》2016年第17期43-48,共6页Chinese Journal of Experimental Traditional Medical Formulae
基 金:湖南省教育厅资助科研项目(14C0709);湖南省教育厅重点项目(10A071);湖南师范大学博士启动基金项目(130668)
摘 要:目的:对白术乙酸乙酯提取物的化学成分进行研究。方法:采用多种现代色谱技术进行分离纯化,通过理化性质及光谱方法鉴定化合物的结构。噻唑蓝(MTT)法对所得化合物进行细胞毒活性测试。结果:从白术的乙酸乙酯提取物中分离得到16个化合物,分别鉴定为1-乙酰氧基-6E,12E-二烯-8,10-二炔-3-醇(1),3-乙酰氧基-6E,12E-二烯-8,10-二炔-1-醇(2),6E,12E-十四碳二烯-8,10-二炔-1,3-二醇乙酸酯(3),12-异戊烯酰氧基-14-乙酰氧-2E,8Z,10E-三烯-4,6-二炔-1醇(4),12-异戊烯酰氧基-14-乙酰氧-2E,8E,10E-三烯-4,6-二炔-1醇(5),白术内酯I(6),白术内酯Ⅱ(7),白术内酯Ⅲ(8),双白术内酯(9),杜松脑(10),蒲公英萜醇乙酸酯(11),3β-乙酰氧基-12-齐墩果烯-11酮(12),7-羟基香豆素(13),二十八烷酸(14),十七烷酸(15),7-ɑ-羟基-β-谷甾醇(16)。结论:化合物1,2,16为首次从白术中分离得到,化合物12~15为首次从苍术属植物中分离得到,化合物6对宫颈癌He La细胞系具有较好抑制作用,IC50为15.6μmol·L^(-1)。Objective: To study the chemical constituents of Atractylodis Macrocephalae Rhizoma.Method: The compounds were isolated and purified from ethyl acetate extract of Atractylodis Macrocephalae Rhizoma by using a combination of chromatographic techniques. Their structures were elucidated on the basis of thierphysico-chemical properties and spectroscopic data analyses. MTT method was used to assay the cytotoxicity agianst He La cells. Result: Sixteen compounds were isolated and purified from ethyl acetate extract of Atractylodis Macrocephalae Rhizoma and determined as 1-acetoxytetradeca-6E, 12E-dien-8, 10-diyn-3-ol( 1), 3-acetoxytetradeca-6E,12E-dien-8,10-diyn-1-ol( 2), tetradeca-6E, 12E-dien-8, 10-diyn-1, 3-diol diacetate( 3), 14-acetoxy-12-senecioyloxytetradeca-2E, 8Z, 10E-trien-4, 6-diyn-1-ol( 4), 14-acetoxy-12-senecioyloxytetradeca-2E,8E,10E-trien-4,6-diyn-1-ol( 5),atractylenolide Ⅰ( 6),atractylenolide Ⅱ( 7),atractylenolide Ⅲ( 8),biatractylenolide( 9),juniper camphor( 10),taraxerylacetate( 11),3β-acetoxy-12-oleanen-11-one( 12),7-hydroxy coumarin( 13),octacosanic acid( 14),heptadecanoic acid( 15),7-α-hydroxyl-β-sitosterol( 16). Conclusion: Among them,compounds 1,2,16 were isolated from the species firstly and compounds 12-15 were isolated from the genus of Atractylodes for the first time. Compound 6 showed good inhibitory activity against He La cells with IC50 values of 15. 6 μmol·L-(-1).
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