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Pyridinyl- and pyridazinyl-3,6-diazabicyclo[3.1.1]heptane-anilines: Novel selective ligands with subnanomolar affinity for ?4?2nACh 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 ?4?2 Ki values ranging from 0.0225 nM (12g) to 2.06 nM (12o).
Iris type:
01.01 Articolo in rivista
Keywords:
3; 6-diazabicyclo[3.1.1]heptanes; Synthesis; Neuronal nicotinic acetylcholine receptors; alpha(4)beta(2) selectivity; Agonism
List of contributors:
Loriga, Giovanni; Fasoli, Francesca; Gotti, Cecilia
Authors of the University:
LORIGA GIOVANNI
Handle:
https://iris.cnr.it/handle/20.500.14243/350802
Published in:
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
Journal
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URL

https://www.ncbi.nlm.nih.gov/pubmed/29751234
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