Cytotoxic oleanane triterpenoids from the rhizomes of Astilbe chinensis (Maxim.) Franch. et Savat.

Abstract:

:Bioassay-guided fractionation of the rhizomes of Astilbe chinensis afforded four cytotoxic pentacyclic triterpenoids, 3beta-hydroxy-olean-12-en-27-oic acid (1), 3beta,6beta-dihydroxy-olean-12-en-27-oic acid (2), 3beta-acetoxy-olean-12-en-27-oic acid (3), and 3beta-hydroxy-urs-12-en-27-oic acid (4). The isolation and purification of these compounds was conducted with the application of column chromatography. Their structures were elucidated on the basis of chemical and spectral evidence. 2D NMR techniques including 1H-1H COSY, HMQC, HMBC spectra and HREIMS were extensively applied to establish the structures. Compounds 1-4 showed cytotoxic activities against HO-8910, Hela and HL60 in vitro; moreover, compound 1 induced apoptotic cell death of the HO-8910 in a dose-dependent manner, ranging from 2.5 to 40.0 microg/ml. The presence of these active compounds may be responsible, at least in part, for the antineoplastic action of the traditional crude drug Rhizoma Astilbe chinensis.

journal_name

J Ethnopharmacol

authors

Sun HX,Ye YP,Pan YJ

doi

10.1016/j.jep.2003.10.003

keywords:

subject

Has Abstract

pub_date

2004-02-01 00:00:00

pages

261-5

issue

2-3

eissn

0378-8741

issn

1872-7573

pii

S0378874103003702

journal_volume

90

pub_type

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