Structure-activity Studies on a Novel Series of Cholinergic Channel Activators Based on a Heteroaryl Ether Framework
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Analogs of compound 1 with a variety of azacycles and heteroaryl groups were synthesized. These analogs exhibited Ki values ranging from 0.15 to > 10,000 nM when tested in vitro for cholinergic channel receptor binding activity (displacement of [3H](-) cytisine from whole rat brain synaptic membranes).
Nicotinic agonists, antagonists, and modulators from natural sources.
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