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15 articles for thisTarget


The following articles (labelled with PubMed ID or TBD) are for your review
PMIDDataArticle TitleOrganization
27894044 37 An insight on synthetic and medicinal aspects of pyrazolo[1,5-a]pyrimidine scaffold.EBI University of Kwazulu-Natal
16610792 15 Refinement of the benzodiazepine receptor site topology by structure-activity relationships of new N-(heteroarylmethyl)indol-3-ylglyoxylamides.EBI Universit£
18851913 11 Azaflavones compared to flavones as ligands to the benzodiazepine binding site of brain GABA(A) receptors.EBI Lund University
19469479 44 Identification of anxiolytic/nonsedative agents among indol-3-ylglyoxylamides acting as functionally selective agonists at the gamma-aminobutyric acid-A (GABAA) alpha2 benzodiazepine receptor.EBI Universita Di Pisa
18651727 15 Synthesis of GABAA receptor agonists and evaluation of their alpha-subunit selectivity and orientation in the GABA binding site.EBI Johannes Gutenberg University
17335185 21 Novel N-substituted indol-3-ylglyoxylamides probing the LDi and L1/L2 lipophilic regions of the benzodiazepine receptor site in search for subtype-selective ligands.EBI Università
15828832 14 High affinity central benzodiazepine receptor ligands: synthesis and biological evaluation of a series of phenyltriazolobenzotriazindione derivatives.EBI Università
12519068 32 Synthesis and benzodiazepine receptor affinity of pyrazolo[1,5-a]pyrimidine derivatives. 3. New 6-(3-thienyl) series as alpha 1 selective ligands.EBI University of Firenze
8355251 8 Synthesis and binding properties of MK-801 isothiocyanates; (+)-3-isothiocyanato-5-methyl-10,11-dihydro-5H-dibenzo[a,d]cyclohepten- 5,10-imine hydrochloride: a new, potent and selective electrophilic affinity ligand for the NMDA receptor-coupled phencyclidine binding site.EBI National Institute of Diabetes and Digestive and Kidney Diseases
3941406 1 Synthesis of alkyl-substituted arecoline derivatives as gamma-aminobutyric acid uptake inhibitors.EBI TBA
28606760 57 Progress in the discovery of small molecule modulators of the Cys-loop superfamily receptors.EBI Amgen
29146472 71 Discovery of the first low-shift positive allosteric modulators for the muscarinic M1 receptor.EBI Roche Pharma Research and Early Development
26950400 37 Design, synthesis and biological evaluation of 1H-pyrrolo[2,3-b]pyridine and 1H-pyrazolo[3,4-b]pyridine derivatives as c-Met inhibitors.BDB Tianjin University of Science and Technology