吴玉德, 张福权, 张梅, 阎乾顺, 黄宝山, 陈仲良. 鹅绒藤酯Ⅰ的分离和测定J. 药学学报, 1991, 26(12): 918-922.
引用本文: 吴玉德, 张福权, 张梅, 阎乾顺, 黄宝山, 陈仲良. 鹅绒藤酯Ⅰ的分离和测定J. 药学学报, 1991, 26(12): 918-922.
YD Wu, FQ Zhang, M Zhang, QS Yan, BS Huang , ZL Chen, . ISOLATION AND IDENTIFICATION OF CYNANESTER A FROM CYNANCHUM CHINENSER.BR.J. Acta Pharmaceutica Sinica, 1991, 26(12): 918-922.
Citation: YD Wu, FQ Zhang, M Zhang, QS Yan, BS Huang , ZL Chen, . ISOLATION AND IDENTIFICATION OF CYNANESTER A FROM CYNANCHUM CHINENSER.BR.J. Acta Pharmaceutica Sinica, 1991, 26(12): 918-922.

鹅绒藤酯Ⅰ的分离和测定

ISOLATION AND IDENTIFICATION OF CYNANESTER A FROM CYNANCHUM CHINENSER.BR.

  • 摘要: 从宁夏产鹅绒藤(Cynanchum chinense R.Br.)地上部分的醇提取物中,分得一新的三萜酯,命名为鹅绒藤酯Ⅰ(cynanester A),经波谱分析和化学反应证明,酯Ⅰ的结构为羽扇醇正己酸酶(l;upeol caproate)。此外还分离鉴定了羽扇醇乙酸酯(lupeol acetate)、正廿四烷酸(lignoceric acid)和β-谷甾醇(β-sitosterol)。

     

    Abstract: Cynanester A (Ⅰ)a new triterpenoid ester was isolated, together with lupeol acetate, lignoceric acid and β-sitosterol, from Cynanchum chinense R. Br. (Asclepiadaceae). The mass spectrum suggested the presence of caproyl group and lupane skeleton with isopropenyl group in the molecule. Alkaline hydrolysis of Ⅰ with 5% methanolic potassium hydroxide yielded lupeol Ia and n- caproic acid. The acid was esterified with MeOH- H2SO4 to afford methyl caproate, by GLC comparison with authentic sample. The acid was also identified by IR comparison. As above, the structure of cynanester A was established as lupeol caproate.

     

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