3-(2-Aminoethyl)pyridine analogs as α4β2 nicotinic cholinergic receptor ligands

3-(2-Aminoethyl)pyridine analogs as α4β2 nicotinic cholinergic receptor ligands A comparison of the binding of three series of nicotinic ligands 3-(4-Aminobutyn-1-yl)pyridines: binding at α4β2 nicotinic cholinergic receptors Aryloxyethylamines: Binding at α7 nicotinic acetylcholine receptors Octahydropyrrolo[3,4-c]pyrrole: A Diamine Scaffold for Construction of Either α4β2 or α7-Selective Nicotinic Acetylcholine Receptor (nAChR) Ligands. Substitutions that Switch Subtype Selectivity Synthesis and structure-activity relationships of pyridine-modified analogs of 3-[2-((S)-pyrrolidinyl)methoxy]pyridine, A-84543, a potent nicotinic acetylcholine receptor agonist Modification of the anabaseine pyridine nucleus allows achieving binding and functional selectivity for the α3β4 nicotinic acetylcholine receptor subtype Binding of nicotine and homoazanicotine analogues at neuronal nicotinic acetylcholinergic (nACh) receptors Chemistry and Pharmacological Characterization of Novel Nitrogen Analogues of AMOP-H-OH (Sazetidine-A, 6-[5-(Azetidin-2-ylmethoxy)pyridin-3-yl]hex-5-yn-1-ol) as α4β2-Nicotinic Acetylcholine Receptor-Selective Partial Agonists 6-(2-Phenylethyl)nicotine: A novel nicotinic cholinergic receptor ligand