Planta Med 2009; 75(15): 1608-1612
DOI: 10.1055/s-0029-1185865
Natural Product Chemistry
Original Paper
© Georg Thieme Verlag KG Stuttgart · New York

Two New Cytotoxic Triterpene Glycosides from the Sea Cucumber Holothuria scabra

Hua Han1 , 2 , Yanghua Yi1 , Qiangzhi Xu3 , Mingping La1 , Hongwei Zhang1
  • 1Research Center for Marine Drugs, School of Pharmacy, Second Military Medical University, Shanghai, P. R. China
  • 2College of Animal Sciences, Zhejiang University, Hangzhou, Zhejiang, P. R. China
  • 3Department of Biochemistry and Molecular Biology, Second Military Medical University, Shanghai, P. R. China
Further Information

Publication History

received Nov. 2, 2008 revised May 23, 2009

accepted June 6, 2009

Publication Date:
13 July 2009 (online)

Abstract

Two new triterpene glycosides, scabraside A (1) and B (2), and a structurally known compound (3), were isolated from the sea cucumber Holothuria scabra (Holothuriidae) collected from the South China Sea. Structure of these compounds was elucidated by spectroscopic and chemical methods. The glycosides 1 and 2 exhibit the same common structural features, i. e., the presence of 12- and 17-hydroxy groups in the holostane-type triterpene aglycone with a 9(11)-ene bond, but are different in the side chains of the triterpene aglycone. The glycosides 1 and 2 had significant in vitro cytotoxicity against four human tumor cell lines in comparison to 10-hydroxycamptothecin.

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Prof. Yanghua Yi

Research Center for Marine Drugs
School of Pharmacy
Second Military Medical University

325 Guo-He Road

Shanghai 200433

People's Republic of China

Phone: + 86 21 65 38 49 88

Fax: + 86 21 65 48 36 62

Email: hhan05@126.com

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