Volume 23, Issue 3 pp. 242-244
Full Paper

12α,13-Dihydroxyolean-3-oxo-28-oic acid, a New Triterpene, and the Known Oleanonic Acid as a New Cell Cycle Inhibitor from Schefflera venulosa

Liu RuiGu Qian-Qun

Gu Qian-Qun

Key Laboratory of Marine Drugs, Ministry of Education, Marine Drug and Food Institute, Ocean University of China, Qingdao, Shandong 266003, China

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Cui Cheng-Bin

Cui Cheng-Bin

Beijing Institute of Pharmacology and Toxicology, Academy of Military Medical Sciences, Beijing 100850, China

Project supported by the National Natural Science Foundation for Distinguished Young Scholars of China (No. 39825126), the Major State Basic Research Development Program (No. 1998051113), and the Cheung Kong Scholar from the Cheung Kong Scholars Program of Ministry of Education of China.

Tel.: 86-532-2032065; Fax: 86-532-2033054

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Cai Bing

Cai Bing

Tianjin Institute for Biomedicinal Research (TIBiR), Tianjin 300384, China

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Liu Hong-Bing

Liu Hong-Bing

Key Laboratory of Marine Drugs, Ministry of Education, Marine Drug and Food Institute, Ocean University of China, Qingdao, Shandong 266003, China

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Wang Lei

Wang Lei

Key Laboratory of Marine Drugs, Ministry of Education, Marine Drug and Food Institute, Ocean University of China, Qingdao, Shandong 266003, China

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Guan Hua-Shi

Guan Hua-Shi

Key Laboratory of Marine Drugs, Ministry of Education, Marine Drug and Food Institute, Ocean University of China, Qingdao, Shandong 266003, China

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First published: 04 April 2005
Citations: 9

Project supported by the National Natural Science Foundation for Distinguished Young Scholars of China (No. 39825126), the Major State Basic Research Development Program (No. 1998051113), and the Cheung Kong Scholar from the Cheung Kong Scholars Program of Ministry of Education of China.

Tel.: 86-532-2032065; Fax: 86-532-2033054

Abstract

12±,13-Dihydroxyolean-3-oxo-28-oic acid (1), a new pentacyclic triterpene, was isolated from Schefflera venulosa (Wight et Arn.) Harms through a bioassay-guided fractionation procedure, together with the known oleanonic acid (2) as a new cell cycle inhibitor. Structures were established by spectroscopy. Compound 2 inhibited the proliferation of K562 cells with the IC50 value of 0.13 µmol/mL by the SRB method and inhibited the cell cycle of tsFT210 cells at the G0/G1 phase at the concentration higher than 10 µg/mL.

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