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DOI: 10.1055/s-0031-1298265
© Georg Thieme Verlag KG Stuttgart · New York
Isolation, Structural Elucidation, and Cytotoxicity of Three New ent-Kaurane Diterpenoids from Isodon japonica var. glaucocalyx
Publication History
received Dec. 8, 2011
revised January 14, 2012
accepted January 22, 2012
Publication Date:
09 February 2012 (online)
Abstract
Three new ent-kaurane diterpenoids, glaucocalyxin H (1), glaucocalyxin I (2), and glaucocalyxin J (3), together with four known diterpenoids (4-7), were isolated from the leaves of Isodon japonica Hara var. glaucocalyx. Their structures were elucidated by spectroscopic analysis, and the structures of compounds 2 and 3 were further confirmed by X-ray crystallographic analysis. Compounds 1, 4, and 5 were evaluated for their cytotoxicity in vitro against CE-1, U87, A-549, MCF-7, Hela, K-562, and HepG-2 human tumor cell lines. Compound 1 showed potent inhibitory activities against six tumor cell lines with IC50 values ranging from 1.86–10.95 µM, and compounds 4 and 5 exhibited significant selective cytotoxicity on seven tumor cell lines.
Key words
Labiatae - Isodon japonica Hara var. glaucocalyx - ent-kaurane diterpenoid - cytotoxicity
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Prof. Dr. Su-Ping Bai
School of Pharmacy
Xinxiang Medical University
Jinsui Avenue East
Xinxiang Henan Province 453003
P. R. China
Phone: +86 0 37 33 02 98 84
Fax: +86 0 37 33 02 98 79
Email: baisuping@xxmu.edu.cn