Journal of Medicinal Chemistry · 2005 · 54 citations · 21 references
MedicineMedicinal ChemistryPharmacologyDrug DiscoveryNeuropharmacologyPsychopharmacologyAnxiolytic PharmacologyGabaergic NeurochemistryGabaergic PharmacologyGabaergic SignalingAnxiolytic Gabaergic AgentsBenzodiazepine Receptor AgonistsGaba AgonistsGaba Receptor AntagonismGaba-a Receptor PharmacologyGaba-b Receptor PharmacologyGabaergic Drug DiscoverySide Effect Profile
There is increasing evidence that compounds with selectivity for gamma-aminobutyric acid(A) (GABA(A)) alpha2- and/or alpha3-subtypes may retain the desirable anxiolytic activity of nonselective benzodiazepines but possess an improved side effect profile. Herein we describe a novel series of GABA(A) alpha2/alpha3 subtype-selective agonists leading to the identification of the development candidate 17, a nonsedating anxiolytic in preclinical animal assays.
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Benzodiazepine actions mediated by specific γ-aminobutyric acidA receptor subtypes
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Medicine, Neuroscience, Pharmacology +14
Insensitivity to anaesthetic agents conferred by a class of GABAA receptor subunit
Paul Davies, Mike C. Hanna, Tim G. Hales et al. · Nature · 1997 · 406 citations