Planta Med 2012; 78(3): 276-285
DOI: 10.1055/s-0031-1280373
Natural Product Chemistry
Original Papers
© Georg Thieme Verlag KG Stuttgart · New York

Spirostanol Saponins Derivated from the Seeds of Trigonella foenum-graecum by β-Glucosidase Hydrolysis and Their Inhibitory Effects on Rat Platelet Aggregation

Xu Pang1 [*] , Yue Cong2 [*] , He-Shui Yu1 , Li-Ping Kang1 , Bing Feng1 , Bing-Xing Han2 , Yang Zhao1 , Cheng-Qi Xiong1 , Da-Wei Tan1 , Wei Song3 , Bin Liu3 , Yu-Wen Cong2 , Bai-Ping Ma1
  • 1Department of Biotechnology, Beijing Institute of Radiation Medicine, Beijing, PR China
  • 2Department of Pathophysiology, Beijing Institute of Radiation Medicine, Beijing, PR China
  • 3School of Chinese Pharmacy, Beijing University of Chinese Medicine, Beijing, PR China
Further Information

Publication History

received July 23, 2011 revised October 19, 2011

accepted October 31, 2011

Publication Date:
29 November 2011 (online)

Abstract

Nine spirostanol saponins (19) and seven mixtures of 25R and 25S spirostanol saponin isomers (1016) were obtained from the seeds of Trigonella foenum-graecum after enzymatic hydrolysis of the furostanol saponin fraction by β-glucosidase. Their structures were determined by NMR and MS spectroscopy. Among them, 1-4, 6, 8, and 9 were new compounds and five, 11b, 12a, 13b, 14a, and 14b, were new structures observed from seven mixtures. In addition, the inhibitory effects of all saponins on rat platelet aggregation were evaluated.

Supporting Information

References

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1 These authors contributed equally to this work.

Prof. Dr. Bai-Ping Ma

Department of Biotechnology
Beijing Institute of Radiation Medicine

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People's Republic of China

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