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中国药学(英文版)

• 【研究论文】 • 上一篇    下一篇

吉祥草中一个新的呋甾皂苷

胡艳维, 王璇, 谢可辉, 涂光忠, 袁丹*, 付宏征*   

  1. 1. 沈阳药科大学 中药学院, 辽宁 沈阳 110016
    2. 北京大学医学部 天然药物及仿生药物国家重点实验室, 北京 100191
    3. 北京微量化学研究所, 北京 100091  
  • 收稿日期:2013-05-02 修回日期:2013-05-15 出版日期:2014-03-13 发布日期:2013-06-25
  • 通讯作者: *Corresponding author. Tel.: 86-24-23986502; 86-10-82805212; Fax: 86-10-82805212; E-mail: yuandan_kampo@163.com; drhzfu@yahoo.com.cn
  • 作者简介:*Corresponding author. Tel.: 86-24-23986502; 86-10-82805212; Fax: 86-10-82805212; E-mail: yuandan_kampo@163.com; drhzfu@yahoo.com.cn
  • 基金资助:
    National Natural Science Foundation of China (Grant No. 81172943).

A new furostanol glycoside from Reineckia carnea 

Yanwei Hu, Xuan Wang, Kehui Xie, Guangzhong Tu, Dan Yuan*, Hongzheng Fu*   

  1. 1. College of Traditional Chinese Medicine, Shenyang Pharmaceutical University, Shenyang 110016, China
    2. State Key Laboratory of Natural and Biomimetic Drugs, Peking University Health Science Center, Beijing 100191, China
    3. Beijing Institute of Microchemistry, Beijing 100091, China
  • Received:2013-05-02 Revised:2013-05-15 Online:2014-03-13 Published:2013-06-25
  • Contact: *Corresponding author. Tel.: 86-24-23986502; 86-10-82805212; Fax: 86-10-82805212; E-mail: yuandan_kampo@163.com; drhzfu@yahoo.com.cn
  • About author:*Corresponding author. Tel.: 86-24-23986502; 86-10-82805212; Fax: 86-10-82805212; E-mail: yuandan_kampo@163.com; drhzfu@yahoo.com.cn
  • Supported by:
    National Natural Science Foundation of China (Grant No. 81172943).

摘要:

对云南产吉祥草的地上部分进行了植物化学研究。针对乙酸乙酯萃取后的水溶液, 利用一系列色谱方法分离得到了一个新呋甾皂苷和四个已知化合物。通过1D NMR、2D NMR, IR和HRESI-MS的方法对分离得到化合物进行了结构鉴定, 分别为 26-O-β-D-glucopyranosyl-(25S)-5β-furost-20(22)-en-1α,3β,26-triol-1-O-α-L-arabinopyranosyl-(1→2)-[α-L-rhamnopyranosyl]-3-O-α-L-rhamnopyranoside (1), (1β,3β,16β,22S)-cholest-5-en-1,3,16,22-tetrol-1,16-di-(β-D-glucopyranoside) (2), diosgenin (3), β-sitosterol (4), ecdysterone (5)。

关键词: 吉祥草, 甾体皂苷, 甾体, 结构鉴定

Abstract:

Phytochemical investigations of the aerial parts of Reineckia carnea, collected in Yunnan Province of China, were conducted to explore new chemical constituents. A series of chromatographic and spectroscopic procedures were utilized on the aqueous solution after partitioned with ethyl acetate, which resulted in the separation of a new furostanol-type glycoside and four known compounds. The structures of the isolated compounds were elucidated on the basis of spectroscopic techniques (1D and 2D NMR, IR, HRESIMS) as 26-O-β-D-glucopyranosyl-(25S)-5β-furost-20(22)-en-1α,3β,26-triol-1-O-α-L-arabinopyranosyl-(1→2)-[α-L-rhamnopyranos-yl]-3-O-α-L-rhamnopyranoside (1), (1β,3β,16β,22S)-cholest-5-en-1,3,16,22-tetrol-1,16-di-(β-D-glucopyranoside) (2), diosgenin (3), β-sitosterol (4), ecdysterone (5).

Key words: Reineckia carnea, Steroidal glycosides, Steroids, Structural identification

中图分类号: 

Supporting: National Natural Science Foundation of China (Grant No. 81172943).