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Pyridinyl- and pyridazinyl-3,6-diazabicyclo[3.1.1]heptane-anilines: Novel selective ligands with subnanomolar affinity for α4β2 nACh receptors

Authors :
Cecilia Gotti
Gérard Aimé Pinna
Miriam Sciaccaluga
Gabriele Murineddu
Francesca Fasoli
Giovanni Loriga
Simona Plutino
Sergio Fucile
Francesco Deligia
Giulio Ragusa
Battistina Asproni
Source :
European journal of medicinal chemistry 152 (2018): 401–416. doi:10.1016/j.ejmech.2018.04.026, info:cnr-pdr/source/autori:Deligia, F.; Murineddu, G.; Gotti, C.; Ragusa, G.; Fasoli, F.; Sciaccaluga, M.; Plutino, S.; Fucile, S.; Loriga, G.; Asproni, B.; Pinna, G. A./titolo:Pyridinyl-and pyridazinyl-3,6-diazabicyclo[3.1.1]heptane-anilines: Novel selective ligands with subnanomolar affinity for ?4<%2Finf>?2<%2Finf>nACh receptors/doi:10.1016%2Fj.ejmech.2018.04.026/rivista:European journal of medicinal chemistry/anno:2018/pagina_da:401/pagina_a:416/intervallo_pagine:401–416/volume:152
Publication Year :
2018
Publisher :
Elsevier BV, 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 α4β2 Ki values ranging from 0.0225 nM (12g) to 2.06 nM (12o).

Details

ISSN :
02235234
Volume :
152
Database :
OpenAIRE
Journal :
European Journal of Medicinal Chemistry
Accession number :
edsair.doi.dedup.....0da655537ee6484da71bef676693dd02
Full Text :
https://doi.org/10.1016/j.ejmech.2018.04.026