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Journal of Chinese Pharmaceutical Sciences

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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).

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

CLC Number: 

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