Planta Med 2009; 75(1): 65-69
DOI: 10.1055/s-0028-1088331
Natural Products Chemistry
Original Paper
© Georg Thieme Verlag KG Stuttgart · New York

Cytotoxic ent-Kaurane Diterpenoids from Isodon henryi

Yong Zhao1 , 2 , 3 , Sheng-Xiong Huang1 , Li-Bin Yang1 , 3 , Jian-Xin Pu1 , Wei-Lie Xiao1 , Li-Mei Li1 , Chun Lei1 , 3 , Zhi-Ying Weng1 , Quan-Bin Han1 , Han-Dong Sun1
  • 1State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming, P. R. China
  • 2College of Chemistry and Engineering, Yunnan Normal University, Kunming, P. R. China
  • 3Graduate University of Chinese Academy of Sciences, Beijing, P. R. China
Weitere Informationen

Publikationsverlauf

Received: August 3, 2007 Revised: July 21, 2008

Accepted: September 12, 2008

Publikationsdatum:
24. November 2008 (online)

Abstract

Chromatographic fractionation of the extract of Isodon henryi resulted in the isolation of seven new ent-kaurane diterpenoids, named minheryins A-G (1 – 7), together with the six known ent-kaurane diterpenoids leukamenin F (8), excisoidesin (9), leukamenin E (10), wangzaozin A (11), pseurata A (12), and racemosin A (13), which were elucidated by spectroscopic analysis. Compounds 7 – 13 were tested for their cytotoxicity against K562 and HepG2 cell lines, and they all exhibited significant activities with IC50 values <0.50 μg/mL. Isolates 1 – 5 were evaluated against the K562 cell line, and only 3 showed weak activity.

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Prof. Han-Dong Sun

State Key Laboratory of Phytochemistry and Plant Resources in West China

Kunming Institute of Botany

Chinese Academy of Sciences

Lanhei Road 132

Kunming 650204

People's Republic of China

Telefon: +86-871-522-3251

Fax: +86-871-521-6343

eMail: hdsun@mail.kib.ac.cn