Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1379592 | Bioorganic & Medicinal Chemistry Letters | 2005 | 5 Pages |
Abstract
An examination of several 3-(2-aminoethyl)pyridine analogs suggests that they likely orient at α4β2 nicotinic cholinergic receptors in a different fashion than their correspondingly substituted nicotine analogs.
Graphical abstractAn examination of several 3-(2-aminoethyl)pyridine analogs 2 (with Ki values ranging from 18 to >10,000 nM) and comparison with their structurally related nicotine analogs 1 suggest that the two series likely bind at nicotinic cholinergic receptors in a different fashion.Figure optionsDownload full-size imageDownload as PowerPoint slide
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Małgorzata Dukat, Anna Ramunno, Rita Banzi, M. Imad Damaj, Billy Martin, Richard A. Glennon,