Back to Search
Start Over
Imidazo[1,2-b][1,2,4]triazines as α2/α3 subtype selective GABAA agonists for the treatment of anxiety
- Source :
- Bioorganic & Medicinal Chemistry Letters. 16:1477-1480
- Publication Year :
- 2006
- Publisher :
- Elsevier BV, 2006.
-
Abstract
- Imidazo[1,2-a]pyrimidines and imidazo[1,2-b][1,2,4]triazines are ligands for the benzodiazepine binding site of GABA(A) receptors that are functionally selective for the alpha2/alpha3 subtypes over the alpha1 subtype. SAR studies to optimise this functional selectivity, pharmacokinetic and behavioural data are described.
- Subjects :
- Male
Agonist
medicine.drug_class
Stereochemistry
Clinical Biochemistry
Administration, Oral
Biological Availability
Pharmaceutical Science
Biochemistry
Anxiolytic
Chemical synthesis
Rats, Sprague-Dawley
Structure-Activity Relationship
Dogs
Drug Discovery
medicine
Functional selectivity
Animals
GABA-A Receptor Agonists
Maze Learning
Receptor
GABA Agonists
Saimiri
Molecular Biology
Binding Sites
Molecular Structure
Bicyclic molecule
Triazines
GABAA receptor
Chemistry
Organic Chemistry
Imidazoles
Receptors, GABA-A
Anxiety Disorders
In vitro
Rats
Disease Models, Animal
Protein Subunits
Molecular Medicine
Ataxia
Female
Subjects
Details
- ISSN :
- 0960894X
- Volume :
- 16
- Database :
- OpenAIRE
- Journal :
- Bioorganic & Medicinal Chemistry Letters
- Accession number :
- edsair.doi.dedup.....ab2e3f49e1fb5468f2d9ea9405f453b8