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Antimuscarinic Effects of (R)- and (S)-Oxyphencyclimine Hydrochloride
Authors:Schjelderup  Lise  Kozlowski  Michael R.  Weissman  Albert  Aasen  Arne J.
Affiliation:(1) Department of Chemistry, The Agricultural University of Norway, Box 30, N 1432 "angst"s-NLH, Norway;(2) Bristol-Myers Company, Wallingford, Connecticut, 06492;(3) Pfizer Central Research, Groton, Connecticut, 06340
Abstract:The (R)-( + )- and (S)-( – )-enantiomers of the anticholinergic compound, oxyphencyclimine, were synthesized from (R)-( – )- and (S)-( + )-2-cyclohexyl-2-hydroxy-2-phenylethanoic acid, respectively. The potencies of the enantiomers were compared using a cholinergic receptor binding assay. The (R)-( + )-enantiomer inhibited binding 29 times more potently than the (S)-( – )-enantiomer.
Keywords:Oxyphencyclimine  enantiomers  anticholinergic  antimuscarinic activity
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