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Pyridinyl- and pyridazinyl-3,6-diazabicyclo[3.1.1]heptane-anilines: Novel selective ligands with subnanomolar affinity for α4β2nACh receptors

Academic Article
Publication Date:
2018
abstract:
The cholinergic pathways in the central nervous system (CNS) of animals and humans are important for cognitive and behavioural functions. Until a few years ago, it was thought that the key molecules transducing the cholinergic message were the metabotropic muscarinic receptors, but it is now known that ionotropic neuronal nicotinic receptors (nAChRs) are also involved. Based on recent studies, we prepared a small library of novel 3-substituted-3,6-diazabicyclo [3.1.1]heptanes, whose binding activity and functionality have been assayed. Among the synthesized compounds, the 3-(anilino)pyridine series resulted in the most interesting compounds with α4β2Kivalues ranging from 0.0225 nM (12g) to 2.06 nM (12o).
Iris type:
1.1 Articolo in rivista
Keywords:
3; 6-diazabicyclo[3.1.1] heptanes; Synthesis; Neuronal nicotinic acetylcholine receptors; α4β2selectivity; Agonism
List of contributors:
Deligia, Francesco; Murineddu, Gabriele; Gotti, Cecilia; Ragusa, Giulio; Fasoli, Francesca; Sciaccaluga, Miriam; Plutino, Simona; Fucile, Sergio; Loriga, Giovanni; Asproni, Battistina; Pinna, Gerard A
Authors of the University:
SCIACCALUGA MIRIAM
Handle:
https://iris.unilink.it/handle/20.500.14085/23187
Published in:
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
Journal
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