Planta Med 2010; 76(14): 1596-1599
DOI: 10.1055/s-0029-1241017
Pharmacology
Letters
© Georg Thieme Verlag KG Stuttgart · New York

Two Prenylated and C-Methylated Flavonoids from Tripterygium wilfordii

Feng Zeng1 , 4 [*] , Wei Wang2 [*] , Yunshan Wu3 , Moul Dey4 , Min Ye1 , Mitchell A. Avery3 , Ikhlas A. Khan2 , De-an Guo1 , 5
  • 1School of Pharmaceutical Sciences, Peking University, Beijing, P. R. China
  • 2Sino-US TCM Research Center, National Center for Natural Products Research, Research Institute of Pharmaceutical Sciences, University of Mississippi, University, MS, USA
  • 3Department of Medicinal Chemistry, University of Mississippi, University, MS, USA
  • 4Biotech Center, Rutgers University, New Brunswick, NJ, USA
  • 5Shanghai Research Center for Modernization of TCM, Shanghai Institute of Materia Medica, CAS, Shanghai, P. R. China
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Publikationsverlauf

received January 8, 2010 revised February 22, 2010

accepted February 24, 2010

Publikationsdatum:
22. März 2010 (online)

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Abstract

Two unusual prenylated and C-methylated flavanones, (±)-5,4′-dihydroxy-2′-methoxy-6′,6′′- dimethypyrano-(2′′,3′′:7,8)-6-methyflavanone (1) and (2S)-5,7,4′-trihydroxy-2′-methoxy-8,5′- di(3-methyl-2-butenyl)-6-methyflavanone (2), and 10 known compounds were isolated from the stems and roots of Tripterygium wilfordii. Their structures were elucidated based on spectroscopic analyses including 1- and 2-D NMR, HR‐ESI‐MS, CD, and x-ray crystallography. The anti-inflammatory, antiproliferative, and antibacterial activities of compounds 1 and 2 were investigated. Compound 2 had an inhibitory effect on lipopolysaccharides (LPS)-triggered RAW cell nitric oxide (NO) production, with an IC50 value of 15.0 ± 0.7 µM. Both compounds showed moderate antiproliferative activity against the tumor cell lines HT-29 and ZR-75-1.

References

1 These authors contributed to this article equally.

Prof. Dr. De-an Guo

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