646066-59-3Relevant articles and documents
Synthesis, in Vitro Affinity, and Efficacy of a Bis 8-Ethynyl-4H-imidazo[1,5a]-[1,4]benzodiazepine Analogue, the First Bivalent α5 Subtype Selective BzR/GABAA Antagonist
Li, Xiaoyan,Cao, Hui,Zhang, Chunchun,Furtmueller, Roman,Fuchs, Karoline,Huck, Sigismund,Sieghart, Werner,Deschamps, Jeffrey,Cook, James M.
, p. 5567 - 5570 (2003)
The synthesis and in vitro affinity of the α5β3γ2 (α5) subtype selective BzR/GABAA antagonist 7 is described. This ligand is selective for α5 subtypes in vitro and is a potent antagonist of the effects of diazepam only at α5β3γ2 subtypes (oocytes). Ligands such as 7 will be important in the determination of which physiological function(s) are subserved by this GABAA α5 subtype.
GABAERGIC AGENTS TO TREAT MEMORY DEFICITS
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Page/Page column 30-31; sheet 1, (2008/06/13)
The present invention provides molecules and methods for the prevention and/or treatment of memory deficit related conditions and/or enhancement of cognizance. In a preferred embodiment, the invention includes compounds, salts and prodrugs thereof for the prevention and/or treatment of these conditions.