Planta Med 2004; 70(10): 967-977
DOI: 10.1055/s-2004-832624
Original Paper
Natural Product Chemistry
© Georg Thieme Verlag KG Stuttgart · New York

New Triterpene Esters from Flowerheads of Arnica lonchophylla

Thomas J. Schmidt1 , Jeanette von Raison1 , Günter Willuhn1
  • 1Institut für Pharmazeutische Biologie der Heinrich-Heine-Universität Düsseldorf, Düsseldorf, Germany
Part of the dissertation of JvR. Some of these results have been presented as posters at the annual meetings of the GA in Regensburg, 1997 and Vienna 1998
Weitere Informationen

Publikationsverlauf

Received: May 4, 2004

Accepted: July 19, 2004

Publikationsdatum:
18. Oktober 2004 (online)

Abstract

From the flowerheads of Arnica lonchophylla Greene ssp. lonchophylla Maguire (Asteraceae), a variety of mono-, di- and trihydroxytriterpenes of the oleanane, ursane, lupane and dammarane types were isolated and their structures elucidated by EI and CI mass spectrometry and extensive NMR spectroscopic analysis. Most of the compounds are esterified at position 3 with lauric, myristic, palmitic and stearic acids. Several ester derivatives of known triterpenes represent new natural products. The triterpenetriols 20(30)-taraxasten-3β,16β,21α-triol (arnitriol A) and lupane-3β,16β,20-triol, both isolated in the form of their C3-fatty acid ester derivatives, possess hydroxylation patterns which have not been described previously. Besides small amounts of triterpenetriol esters, the lauric, myristic, palmitic and stearic acid esters of arnidiol, faradiol, maniladiol and calenduladiol were also identified in the flowerheads of A. montana (Arnicae flos Ph. Eur.), A. chamissonis ssp. foliosa and A. angustifolia ssp. attenuata. A search for sesquiterpene lactones in the flowers of A. lonchophylla resulted in the identification of small amounts of helenalin and 11α,13-dihydrohelenalin.

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Priv.-Doz. Dr. Thomas J. Schmidt

Institut für Pharmazeutische Biologie der Heinrich-Heine-Universität Düsseldorf

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40225 Düsseldorf

Germany

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eMail: schmidtt@uni-duesseldorf.de