The Preparation and Human Muscarinic Receptor Profiling of Oxybutynin and N-Desethyloxybutynin Enantiomers

Author(s): Allen B. Reitz , Suneel K. Gupta , Yifang Huang , Michael H. Parker , Richard R. Ryan .

Journal Name: Medicinal Chemistry

Volume 3 , Issue 6 , 2007

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Abstract:

Oxybutynin (1) is a non-selective muscarinic receptor antagonist that is used clinically for the treatment of urinary incontinence. The major metabolite of oxybutynin in humans is desethyloxybutynin (2). We have prepared the enantiomers of 1 and 2 and evaluated their ability to displace N-CT3-scopolamine chloride (3H-NMS) binding on human cloned muscarinic m1-5 receptors. Compounds 1 and 2 potently displaced 3H-NMS binding at m1, m3 and m4 receptors, but were less potent at the m2 and m5 subtypes. However, metabolite 2 was more potent than the parent compound 1 in the binding assay. In general the R enantiomers were more potent than their respective S enantiomers. Therefore, we suggest that the cholinergic side effects associated with 2 may be due to its greater apparent potency with m1 and m3 receptors, especially of its R-enantiomer, when compared with parent drug 1.

Keywords: CHO cells, muscarinic receptors, desethyloxybutynin, oxybutynin therapy, binding assay

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Article Details

VOLUME: 3
ISSUE: 6
Year: 2007
Page: [543 - 545]
Pages: 3
DOI: 10.2174/157340607782360353
Price: $58

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