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走马胎中的三萜皂苷类成分及其体外抗肿瘤活性研究
引用本文:穆丽华,赵海霞,龚强强,周小江,刘屏.走马胎中的三萜皂苷类成分及其体外抗肿瘤活性研究[J].解放军药学学报,2011,27(1):1-6.
作者姓名:穆丽华  赵海霞  龚强强  周小江  刘屏
作者单位:1. 解放军总医院药理研究室,北京,100853
2. 天津中医药大学,天津,300193
基金项目:国家自然科学基金资助项目,No.31000153
摘    要:目的 研究走马胎根茎的三萜皂苷类成分及其体外抗肿瘤活性.方法 采用溶剂萃取和柱色谱方法分离纯化,根据理化性质和波谱学数据鉴定化合物结构.采用MTT法测试三萜皂苷化合物的抗肿瘤活性.结果 分离得到了7个三萜皂苷类化合物,包括3β-O- β-D-吡喃木糖基-(1→2)-β-D-吡喃葡萄糖基-(1→4)-α-L-吡喃阿拉伯糖...

关 键 词:走马胎  化学成分  皂苷  抗肿瘤活性  MTT法

Triterpenoid Saponins and the Antitumor Activity from the Rhizome of Ardisia Gigantifolia Stapf
MU Li-hua,ZHAO Hai-xia,GONG Qiang-qiang,ZHOU Xiao-jiang,LIU Ping.Triterpenoid Saponins and the Antitumor Activity from the Rhizome of Ardisia Gigantifolia Stapf[J].Pharmaceutical Journal of Chinese People's Liberation Army,2011,27(1):1-6.
Authors:MU Li-hua  ZHAO Hai-xia  GONG Qiang-qiang  ZHOU Xiao-jiang  LIU Ping
Institution:MU Li-hua,ZHAO Hai-xia,GONG Qiang-qiang,ZHOU Xiao-jiang,LIU PingDepartment of Clinical Pharmacology,General Hospital of PLA,Beijing ,China,Tianjin University of Traditional Chinese Medicine,Tianjin
Abstract:Objective To study triterpenoid saponins and the antitumor activity of the 60% ethanol extract of the rhizome of Ardisia gigantifolia Stapf.Methods The chemical components were isolated by solvent extraction and column chromatography and their structures were identified on the basis of physical-chemical constants and spectral data.The antitumor activities of the compounds were screened by MTT methods.Results Seven triterpenoid saponins were isolated and identified as 3β-O-{β-D-xylopyranosyl-(1→2)-β-D-glucopyr-anosyl-(1→4)-α-L-arabinopyranosyl}-3β-hydroxy-13β,28-epoxy-16β-hydroxy-30-al(1);cyclamiretin A 3β-O-α-L-rhamnopyranosyl(1→3)-β-D-xylopyranosyl-(1→2)]-β-D-glucopyranosyl-(1→4)-β-D-glucopyranosyl(1→2)]-α-L-arabinopyranoside(2);lysikoianoside(3);cyclamiretin A 3β-O-α-L-rhamnopyranosyl-(1→3)-β-D-glucopyranosyl-(1→3)-β-D-xylopyranosyl-(1→2)]-β-D-glucopyranosyl-(1→4)-β-D-glucopyranosyl-(1→2)]-α-L-arabinopyranoside(4),3β-O-{α-L-rhamnopyranosyl-(1→3)-β-D-xylopyranosyl-(1→2)]-β-D-galactopyranosyl-(1→4)-β-D-6-O-acetyl-glucopranosyl-(1→2)]-α-L-arabinopyranoside}-cyclamiretin A(5),Ardisiacri-dpin A(6) and 3β-o-{α-L-rhamnopyranosyl-(1→3)-β-D-xylopyranose-(1→2)]-β-D-glucopyranosyl-(1→4)-α-L-arabinopyranosyl}-3β-hydroxy-13β,28-epoxyoleanan-16-oxo-30-al(7).Conclusion Compound 1 and 3 were obtained from this plant and 7 from this genus for the first time.Among the compounds,No.2 showed cytotoxic activity of 0.29,9.99 and 2.03 μg/ml(IC50) in BCG-823,EJ and Hepg2 cells respectively.Compound 3 showed selective cytotoxic activity to EJ cells(IC50 7.20 μg/ml).Compound 7 showed cytotoxic activity of 8.53 μg/ml(IC50) in Hepg2 cells.
Keywords:Ardisia gigantifolia Stapf  chemical constitutents  triterpenoid saponins  antitumor activity  MTT methods  
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