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).
Publication types
-
Research Support, Non-U.S. Gov't
MeSH terms
-
Animals
-
Bonamia Plant*
-
Carbachol
-
Female
-
Gastrointestinal Motility / drug effects*
-
Guinea Pigs
-
Ileum / metabolism
-
Magnetic Resonance Spectroscopy
-
Male
-
Monoterpenes / administration & dosage
-
Monoterpenes / chemistry
-
Monoterpenes / pharmacology*
-
Monoterpenes / therapeutic use
-
Muscarinic Antagonists / administration & dosage
-
Muscarinic Antagonists / chemistry
-
Muscarinic Antagonists / pharmacology*
-
Muscarinic Antagonists / therapeutic use
-
Phytotherapy*
-
Plant Extracts / administration & dosage
-
Plant Extracts / chemistry
-
Plant Extracts / pharmacology*
-
Plant Extracts / therapeutic use
-
Plant Roots
-
Receptor, Muscarinic M3 / antagonists & inhibitors*
Substances
-
Monoterpenes
-
Muscarinic Antagonists
-
Plant Extracts
-
Receptor, Muscarinic M3
-
bonabiline A
-
Carbachol