Planta Med 2012; 78(5): 480-484
DOI: 10.1055/s-0031-1298201
Natural Product Chemistry
Letters
© Georg Thieme Verlag KG Stuttgart · New York

Four New Cytotoxic Tetrahydrofuranoid Lignans from Sinopodophyllum emodi

Yan-Jun Sun1 , 2 , 3 , Zhan-Lin Li1 , 2 , Hong Chen4 , 5 , Xiao-Qiu Liu2 , Wei Zhou1 , 2 , Hui-Ming Hua1 , 2
  • 1Key Laboratory of Structure-Based Drug Design & Discovery, Ministry of Education, Shenyang Pharmaceutical University, Shenyang, PR China
  • 2School of Traditional Chinese Materia Medica, Shenyang Pharmaceutical University, Shenyang, PR China
  • 3School of Pharmacy, Henan College of Traditional Chinese Medicine, Zhengzhou, PR China
  • 4Tianjin Key Laboratory for Biomarkers of Occupational and Environmental Hazard, Tianjin, PR China
  • 5Pharmacognosy Division, Medical College of Chinese People's Armed Police Force, Tianjin, PR China
Further Information

Publication History

received October 12, 2011 revised December 8, 2011

accepted January 3, 2012

Publication Date:
26 January 2012 (online)

Zoom Image

Abstract

Four new tetrahydrofuranoid lignans, (−)-tanegool-7′-methyl ether (1), (+)-7′-methoxylariciresinol (2), sinolignan C (3), and epipinoresinol-4,4′-di-O-β-D-glucopyranoside (4), were isolated from the roots and rhizomes of Sinopodophyllum emodi together with one known lignan (5). Their structures and stereochemistry were elucidated on the basis of spectroscopic and mass spectrometric evidence. The isolation of compounds 15 represents the first report of tetrahydrofuran lignans from the genus Sinopodophyllum. The cytotoxic activities of all isolated compounds were evaluated against HeLa and KB cell lines, and compound 1 showed the most potent cytotoxicity with IC50 values of 9.7 µM and 4.7 µM, respectively.

Supporting Information