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DOI: 10.1055/s-2004-832614
© Georg Thieme Verlag KG Stuttgart · New York
Inhibition of Leukotriene Biosynthesis by Quinolone Alkaloids from the Fruits of Evodia rutaecarpa
Publikationsverlauf
Received: April 20, 2004
Accepted: July 8, 2004
Publikationsdatum:
18. Oktober 2004 (online)
Abstract
The n-hexane extract of the fruits of Evodia rutaecarpa showed a considerable inhibiting effect on leukotriene biosynthesis in human granulocytes. Bioassay-guided fractionation of the extract led to the isolation of the 5 quinolone alkaloids: 1-methyl-2-nonyl-4(1H)-quinolinone, 1-methyl-2-(6Z)-6-undecenyl-4(1H)-quinolinone, 1-methyl-2-(4Z,7Z)-4,7-tridecadienyl-4(1H)-quinolinone, evocarpine and 1-methyl-2-(6Z,9Z)-6,9-pentadecadienyl-4(1H)-quinolinone. The compounds exhibited inhibitory activity on leukotriene biosynthesis in a bioassay using human polymorphonuclear granulocytes, with IC50 values of 12.1, 10.0, 10.1, 14,6 and 12.3 μM, respectively. Structure elucidation of the compounds was achieved by 1D and 2D NMR experiments and comparison of spectral data with literature data.
Key words
Evodia rutaecarpa - Rutaceae - leukotriene biosynthesis - quinolone alkaloids - traditional Chinese medicine (TCM)
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Prof. Dr. Rudolf Bauer
Institute of Pharmaceutical Sciences
Department of Pharmacognosy
Karl-Franzens-Universität Graz
Universitätsplatz 4
8010 Graz
Austria
eMail: rudolf.bauer@uni-graz.at