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30 articles for thisTarget


The following articles (labelled with PubMed ID or TBD) are for your review
PMIDDataArticle TitleOrganization
26101564 20 MLN8054 and Alisertib (MLN8237): Discovery of Selective Oral Aurora A Inhibitors.EBI Takeda Pharmaceutical
23121096 86 Ion channels as therapeutic targets: a drug discovery perspective.EBI Pfizer
22734650 6 Allyl m-trifluoromethyldiazirine mephobarbital: an unusually potent enantioselective and photoreactive barbiturate general anesthetic.EBI Massachusetts General Hospital
18537233 108 Selective influence on contextual memory: physiochemical properties associated with selectivity of benzodiazepine ligands at GABAA receptors containing the alpha5 subunit.EBI Moltech
21277199 29 Exploring subtype selectivity and metabolic stability of a novel series of ligands for the benzodiazepine binding site of the GABAA receptor.EBI Novartis Institutes For Biomedical Research
 7 A conformational study of ligands for omega modulatory sites of GABAa receptors by NOESY NMR spectroscopy and distance geometryEBI TBA
17626010 4 Proximity-accelerated chemical coupling reaction in the benzodiazepine-binding site of gamma-aminobutyric acid type A receptors: superposition of different allosteric modulators.EBI University of Bern
17311911 2 Identification of anesthetic binding sites on human serum albumin using a novel etomidate photolabel.EBI Imperial College
12408715 97 Synthesis and biological evaluation of 7,8,9,10-tetrahydroimidazo[1,2-c]pyrido[3,4-e]pyrimdin-5(6H)-ones as functionally selective ligands of the benzodiazepine receptor site on the GABA(A) receptor.EBI Neurogen
31404862 138 Imidazopyridine-based selective and multifunctional ligands of biological targets associated with psychiatric and neurodegenerative diseases.EBI Palack£
31738537 95 Subtype Selective ?-Aminobutyric Acid Type A Receptor (GABAEBI University of Sussex
28759875 30 An overview of benzo[b]thiophene-based medicinal chemistry.EBI Jain University
26833890 18 Synthesis, Biological Evaluation, and Molecular Docking of 8-imino-2-oxo-2H,8H-pyrano[2,3-f]chromene Analogs: New Dual AChE Inhibitors as Potential Drugs for the Treatment of Alzheimer's Disease.BDB Yogi Vemana University
26469307 7 Phosphorylation of Capsaicinoid Derivatives Provides Highly Potent and Selective Inhibitors of the Transcription Factor STAT5b.BDB University of Leipzig
26214255 11 The amylase inhibitor montbretin A reveals a new glycosidase inhibition motif.BDB University of British Columbia
25636004 12 Structure-guided design of a high affinity inhibitor to human CtBP.BDB University of Massachusetts Medical School