Planta Med 2012; 78(17): 1878-1880
DOI: 10.1055/s-0032-1315369
Natural Product Chemistry
Letters
Georg Thieme Verlag KG Stuttgart · New York

Three New Sesquiterpenes with Cytotoxic Activity from Dobinea delavayi

Zhong-Quan Cheng
2   State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, The Chinese Academy of Sciences, Kunming, P. R. China
3   Department of Chemistry and Engineering, Guilin Normal College, Guilin, P. R. China
,
Dan Yang
3   Department of Chemistry and Engineering, Guilin Normal College, Guilin, P. R. China
,
Qing-Yun Ma
1   Institute of Tropical Bioscience and Biotechnology, Chinese Academy of Tropical Agricultural Sciences, Haikou, P. R. China
,
Hao-Fu Dai
1   Institute of Tropical Bioscience and Biotechnology, Chinese Academy of Tropical Agricultural Sciences, Haikou, P. R. China
,
Sheng-Zhuo Huang
1   Institute of Tropical Bioscience and Biotechnology, Chinese Academy of Tropical Agricultural Sciences, Haikou, P. R. China
,
Xiang-Hui Yi
3   Department of Chemistry and Engineering, Guilin Normal College, Guilin, P. R. China
,
Jun Zhou
2   State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, The Chinese Academy of Sciences, Kunming, P. R. China
,
You-Xing Zhao
1   Institute of Tropical Bioscience and Biotechnology, Chinese Academy of Tropical Agricultural Sciences, Haikou, P. R. China
› Author Affiliations
Further Information

Publication History

received 05 May 2012
revised 09 August 2012

accepted 22 August 2012

Publication Date:
21 September 2012 (online)

Abstract

Three new sesquiterpenes dobinins A–C (13), together with five known compounds, were isolated from the root of Dobinea delavayi. The structures of the three new compounds were determined on the basis of spectroscopic analysis including 1D-, 2D-NMR and MS techniques as well as by comparison of the spectral data with those of analogous compounds reported in the literatures. Compounds 13 were screened for antitumor activity in vitro and exhibited definite cytotoxic activity against the human tumor cell line HL-60 with IC50 levels of 8.0 × 10−5, 4.7 × 10−5, and 5.1 × 10−5 M, respectively.

Supporting Information