New Insight into the Central Benzodiazepine Receptor–Ligand Interactions: Design, Synthesis, Biological Evaluation, and Molecular Modeling of 3-Substituted 6-Phenyl-4H-imidazo[1,5-a][1,4]benzodiazepines and Related Compounds
doi: 10.1021/jm2001597
pmid: 21751815
handle: 11588/403324 , 20.500.14243/53357 , 11365/18931 , 11568/205355 , 2158/960443
doi: 10.1021/jm2001597
pmid: 21751815
handle: 11588/403324 , 20.500.14243/53357 , 11365/18931 , 11568/205355 , 2158/960443
New Insight into the Central Benzodiazepine Receptor–Ligand Interactions: Design, Synthesis, Biological Evaluation, and Molecular Modeling of 3-Substituted 6-Phenyl-4H-imidazo[1,5-a][1,4]benzodiazepines and Related Compounds
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 K(i) values spanning from the low nanomolar to the submicromolar range. In particular, imidazoester 5f was able to promote a massive flow of (36)Cl(-) 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 α(1)β(2)γ(2)L, α(2)β(1)γ(2)L, and α(5)β(2)γ(2)L human GABA(A) receptors. Finally, some compounds were submitted to molecular docking calculations along with molecular dynamics simulations in the Cromer's GABA(A) homology model.
- National Research Council Italy
- University of Cagliari Italy
- University of Siena Italy
- University of Pisa Italy
- Magna Graecia University Italy
Cerebral Cortex, Flumazenil, Male, Models, Molecular, Binding Sites, Molecular Structure, Motor Activity, Ligands, Receptors, GABA-A, Binding, Competitive, Protein Structure, Tertiary, Benzodiazepines, Mice, Protein Subunits, Radioligand Assay, HEK293 Cells, Chlorides, benzodiazepine receptor, Animals, Humans, Cattle
Cerebral Cortex, Flumazenil, Male, Models, Molecular, Binding Sites, Molecular Structure, Motor Activity, Ligands, Receptors, GABA-A, Binding, Competitive, Protein Structure, Tertiary, Benzodiazepines, Mice, Protein Subunits, Radioligand Assay, HEK293 Cells, Chlorides, benzodiazepine receptor, Animals, Humans, Cattle
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