Article ID Journal Published Year Pages File Type
10596989 Bioorganic & Medicinal Chemistry Letters 2005 4 Pages PDF
Abstract
A series of derivatives of (7R,9S)-(−)-cytisine were evaluated for affinity and function at several subtypes of nicotinic receptors. Substitution-dependent changes in potency, efficacy, and selectivity were seen.
Related Topics
Physical Sciences and Engineering Chemistry Organic Chemistry
Authors
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