Planta Med 2006; 72(5): 450-457
DOI: 10.1055/s-2005-916263
Original Paper
Natural Product Chemistry
© Georg Thieme Verlag KG Stuttgart · New York

New Triterpenoids from Kadsura heteroclita and their Cytotoxic Activity

Wei Wang1 , 2 , Jinzhi Liu3 , Jian Han1 , Zhengren Xu1 , Rongxia Liu2 , Peng Liu1 , Weixing Wang1 , Xiaochi Ma2 , Shuhong Guan2 , Dean Guo1 , 2
  • 1School of Pharmaceutical Sciences, Peking University, Beijing, P. R. China
  • 2Shanghai Research Center for Modernization of Traditional Chinese Medicine, Shanghai Institute of Materia Medica, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai, P. R. China
  • 3Peking University Shenzhen Hospital, Shenzhen City, Guangdong Province, P. R. China
Further Information

Publication History

Received: March 19, 2005

Accepted: November 17, 2005

Publication Date:
10 February 2006 (online)

Abstract

Phytochemical investigations of the stem of Kadsura heteroclita (Roxb) Craib (Schizandraceae) resulted in the isolation and structure elucidation of six new triterpenoidal compounds named heteroclitalactones A - E (1 - 5) as well as heteroclic acid (6) and heteroclitalactone F (7), which was isolated for the first time from a natural source, and the six known compounds schisanlactone E (8), cycloartenone (9), schisandronic acid (10), nigranoic acid (11), changnanic acid (12) and schisanlactone B (13), respectively. The structures of these compounds were characterized by extensive 1D and 2D NMR spectral analyses. The majority of these triterpenoids showed moderate cytotoxic activity against the human tumor cell lines Bel-7402, BGC-823, MCF-7 and HL-60. Among the compounds tested, heteroclitalactone D (4) showed the strongest cytotoxic activity against the HL-60 cells with an IC50 of 6.76 μM.

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Prof. Dr. Dean Guo

School of Pharmaceutical Sciences

Peking University

Xueyuan Road 38

Beijing 100083

People’s Republic of China

Phone: +86-10-8280-2024

Fax: +86-10-8280-2700

Email: gda@bjmu.edu.cn

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