期刊文献+

蝙蝠葛中的多巴胺能生物碱(英文) 被引量:1

Dopaminergic Alkaloids from Menispermum dauricum
原文传递
导出
摘要 目的:研究中药蝙蝠葛的化学成分。方法:应用硅胶和凝胶反复柱层析进行分离,分得成分用波谱分析和理化性质对照进行结构鉴定。结果:分离鉴定出8种成分,分别为meniscoside(1),dauricoside(2),dauriporphine(3),menisporphine(4),bianfugecine(5),2,3-dihydromenisporphine(6),syringaresinol(7)和syringaresinol4,4′-O-bis-glucoside(8)。结论:化合物1为新的苄基异喹啉生物碱葡萄糖苷,首次报道化合物1-6在对多巴胺D1和D2受体竞争性结合实验中,表现出对D1受体明显的选择性结合,其中1和2的IC50分别为9.2和2.0μmol?L-1。 AIM:To study the bioactive components of the rhizoma of Menispermum dauricum.METHODS:Repeated column chromatography was used for the separation of the compounds and various spectroscopic techniques were applied for structural determination.RESULTS:Eight compounds,meniscoside(1),dauricoside(2),dauriporphine(3),menisporphine(4),bianfugecine(5),2,3-dihydromenisporphine(6),syringaresinol(7),and syringaresinol 4,4'-O-bis-glucoside(8) were obtained and identified.The effects on D1 and D2 receptors labeled with [3H] were evaluated.CONCLUSION:Compound 1 was a new glucosidic benzylisoquinoline.Compounds 1-6 showed significant selective affinity to D1 receptor,and the IC50 of 1 and 2 were 9.2 and 2.0 μmol?L-1,respectively.
出处 《中国天然药物》 SCIE CAS CSCD 北大核心 2011年第4期249-252,共4页
基金 supported by National Natural Sciences Foundation of China(No.30470187)~~
关键词 蝙蝠葛 Meniscoside 多巴胺D1和D2受体 生物碱 Menispermum dauricum Meniscoside Effects on D1 and D2 receptors Alkaloid
  • 相关文献

参考文献9

  • 1Protais P, Cortes D, Pon JL, et al. Displacement activity of some natural cularine alkaloids at striatal 3H-SCH 23390 and ^3H-raclopride binding sites [J]. Experientia, 1992, 48(1): 27-30.
  • 2Cortes D, Figadere B, Saez J, et al. Displacement activity of bisbenzylisoquinoline alkaloids at striatal ^3H-SCH23390 and ^3H-raclopride binding sites [J]. J Nat Prod, 1992, 55(9): 1281-1286.
  • 3Cortes D, Arbaoui J, Protais P. High affinity and selectivity of some tetrahydroprotoberberine alkaloids for rat striatal ^3H-raclopride binding sites [J]. Nat Prod Lett, 1993, 3(4): 233-238.
  • 4Hu SM, Xu SX, Yao XS, et al. Dauricoside, a new glycosidal alkaloid having an inhibitory activity blood-platelet aggrega- tion [J]. Chem Pharma Bull, 1993, 41(10): 1866-1868.
  • 5Kunitomo J, Satoh M. Structure and synthesis of menispor- phine, a new type of isoquinoline alkaloid [J]. Tetrahedron, 1983, 39(20): 3261-3265.
  • 6Kunitomo J, Kaede S, Satoh M. The structure of 2 3-dihydromenisporphine and the synthesis dauriporphine oxoisoaporphine alkaloids from Menispermum dauricum [J] Chem Pharm Bull, 1985, 33(7): 2778-2782.
  • 7Hou C, Xue H. Studies on the Chemical constituents of Menis- permum dauricum [J]. Acta Pharm Sin, 1985, 20(2): 112-117.
  • 8Barbara V, Otto S, Hildebert W. Synthesis of biological active tetrahydrofurofuranliganan-(syringin, pinoresinol)-mono-and bis- glucosides [J]. Phytochemistry, 1991,30(9): 3087-3089.
  • 9Brochmann-Hanssen E, Nielsen B. (+)-Reticuline-a new opium alkaloid [J]. Tetrahedron Lett, 1965, 6(18): 1271 - 1274.

同被引文献8

引证文献1

二级引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部