Novel N-aryl nicotinamide derivatives: Taking stock on 3,6-diazabicyclo[3.1.1]heptanes as ligands for neuronal acetylcholine receptors

摘要

We designed the synthesis of a small library of 3-substituted-3,6-diazabicyclo[3.1.1]heptanes whose affinity on neuronal nicotinic receptors (nAChRs) was evaluated. Among the synthesized compounds, the 5-(3,6-diazabicyclo[3.1.1]heptane-3-yl)-N-(2-fluorophenyl)nicotinamide 43 proved to be the most interesting compound with alpha(4)beta(2) Ki value of 10 pM and a very high alpha(7)/alpha(4)beta(2) selectivity. Furthermore, compounds 35, 39 and 43 elicited a selective partial agonist activity for alpha(4)beta(2) nAChR subtype.