1318262-20-2Relevant articles and documents
New insight into the central benzodiazepine receptor-ligand interactions: Design, synthesis, biological evaluation, and molecular modeling of 3-substituted 6-phenyl-4 H -imidazo[1,5- a][1,4]benzodiazepines and related compounds
Anzini, Maurizio,Valenti, Salvatore,Braile, Carlo,Cappelli, Andrea,Vomero, Salvatore,Alcaro, Stefano,Ortuso, Francesco,Marinelli, Luciana,Limongelli, Vittorio,Novellino, Ettore,Betti, Laura,Giannaccini, Gino,Lucacchini, Antonio,Daniele, Simona,Martini, Claudia,Ghelardini, Carla,Di Cesare Mannelli, Lorenzo,Giorgi, Gianluca,Mascia, Maria Paola,Biggio, Giovanni
, p. 5694 - 5711 (2011/10/08)
3-Substituted 6-phenyl-4H-imidazo[1,5-a][1,4]benzodiazepines and related compounds were synthesized as central benzodiazepine receptor (CBR) ligands. Most of the compounds showed high affinity for bovine and human CBR, their Ki values spanning from the low nanomolar to the submicromolar range. In particular, imidazoester 5f was able to promote a massive flow of 36Cl- in rat cerebrocortical synaptoneurosomes overlapping its efficacy profile with that of a typical full agonist. Compound 5f was then examined in mice for its pharmacological effects where it proved to be a safe anxiolytic agent devoid of the unpleasant myorelaxant and amnesic effects of the classical 1,4-benzodiazepines. Moreover, the selectivity of some selected compounds has been assessed in recombinant α1β 2γ2L, α2β1γ 2L, and α5β2γ2L human GABAA receptors. Finally, some compounds were submitted to molecular docking calculations along with molecular dynamics simulations in the Cromer's GABAA homology model.
