Planta Med 2006; 72(15): 1403-1406
DOI: 10.1055/s-2006-951728
Original Paper
Pharmacology
© Georg Thieme Verlag KG Stuttgart · New York

Bonabiline A, a Monoterpenoid 3α-Acyloxytropane from the Roots of Bonamia spectabilis showing M3 Receptor Antagonist Activity

Sonja C. Ott1 , Kristina Jenett-Siems1 , Heinz H. Pertz1 , Karsten Siems2 , Ludger Witte†3 , Eckart Eich1
  • 1Institut für Pharmazie (Pharmazeutische Biologie), Freie Universität Berlin, Berlin, Germany
  • 2AnalytiCon Discovery, Potsdam, Germany
  • 3Institut für Pharmazeutische Biologie, Technische Universität Braunschweig, Braunschweig, Germany
Part 21 in the series “Phytochemistry and Chemotaxonomy of the Convolvulaceae”. For part 20, see Ott et al., submitted to Z Naturforsch B
Further Information

Publication History

Received: June 29, 2006

Accepted: September 26, 2006

Publication Date:
06 November 2006 (online)

Abstract

Two 3α-acyloxytropanes with unique monoterpenoic acyl moieties, bonabiline A and its anhydro derivative bonabiline B, have been isolated from the roots of Bonamia spectabilis. Their structures were elucidated by detailed spectroscopic analysis. Due to the structural similarity of bonabiline A to atropine/hyoscyamine, the affinity of both bonabilines to the muscarinic M3 receptor was studied in the isolated guinea-pig ileum. Bonabiline A (pA2 6.65 ± 0.03) proved to be a more potent antagonist than bonabiline B (pA2 5.50 ± 0.03).

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Prof. Dr. Eckart Eich

Institut für Pharmazie (Pharmazeutische Biologie)

Freie Universität Berlin

Königin-Luise-Str. 2 – 4

14195 Berlin

Germany

Fax: +49-30-8385-1461

Email: eckeich@zedat.fu-berlin.de

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