1. Academic Validation
  2. Cytotoxic isoprenylated xanthones from Cudrania tricuspidata

Cytotoxic isoprenylated xanthones from Cudrania tricuspidata

  • Bioorg Med Chem. 2004 Apr 15;12(8):1947-53. doi: 10.1016/j.bmc.2004.01.030.
Ying-Shu Zou 1 Ai-Jun Hou Guo-Fu Zhu Yan-Feng Chen Han-Dong Sun Qin-Shi Zhao
Affiliations

Affiliation

  • 1 Department of Pharmacognosy, School of Pharmacy, Fudan University, 138 Yi Xue Yuan Road, Shanghai 200032, People's Republic of China.
Abstract

Eight new isoprenylated Xanthones, cudratricusxanthones A-H (1-8), were isolated from the roots of Cudrania tricuspidata, together with ten known compounds, cudraxanthones H (9) and M (10), xanthone V(1a) (11), toxyloxanthone C (12), macluraxanthone B (13), 1-hydroxy-3, 6, 7-trimethoxyxanthone (14), cycloartocarpesin (15), artocarpesin (16), cudraflavone B (17), and kaempferol (18). Their structures were characterized by spectroscopic methods. Xanthones 5, 7, 10, and 12 showed inhibitory effects on four kinds of human digestive apparatus tumor cell lines (HCT-116, SMMC-7721, SGC-7901, and BGC-823) with IC(50) values of 1.6-11.8 microg/mL. Xanthones 2, 4, and 11 displayed significant cytotoxicity against HCT-116, SMMC-7721, and SGC-7901 (IC(50)=1.3-9.8 microg/mL). Flavonoids 15-17 were almost inactive.

Figures
Products