| Literature DB >> 17089324 |
Sonja C Ott1, Kristina Jenett-Siems, Heinz H Pertz, Karsten Siems, Ludger Witte, Eckart Eich.
Abstract
Two 3alpha-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 M (3) receptor was studied in the isolated guinea-pig ileum. Bonabiline A (pA (2) 6.65 +/- 0.03) proved to be a more potent antagonist than bonabiline B (pA (2) 5.50 +/- 0.03).Entities:
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Year: 2006 PMID: 17089324 DOI: 10.1055/s-2006-951728
Source DB: PubMed Journal: Planta Med ISSN: 0032-0943 Impact factor: 3.352