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15 articles for thisTarget

The following articles (labelled with PubMed ID or TBD) are for your review
PMIDDataArticle TitleOrganization
27994728 23 Pyrazole Inhibitors of GluN2B NMDA Receptor Subunit.EBI Dart Neuroscience
27061977 8 Benzimidazolone bioisosteres of potent GluN2B selective NMDA receptor antagonists.EBI Institut F£R Pharmazeutische Und Medizinische Chemie Der Universit£T M£Nster
25458498 29 Synthesis, GluN2B affinity and selectivity of benzo[7]annulen-7-amines.EBI Institut F£R Pharmazeutische Und Medizinische Chemie Der Universit£T M£Nster
22366657 39 A novel series of benzimidazole NR2B-selective NMDA receptor antagonists.EBI Glaxosmithkline
21524576 69 2,6-Disubstituted pyrazines and related analogs as NR2B site antagonists of the NMDA receptor with anti-depressant activity.EBI Astrazeneca Pharmaceuticals
19648007 3 Synthesis and evaluation of novel tricyclic benzo[4.5]cyclohepta[1.2]pyridine derivatives as NMDA/NR2B antagonists.EBI Merck Research Laboratories
17498948 24 Cyclic benzamidines as orally efficacious NR2B-selective NMDA receptor antagonists.EBI Merck Research Laboratories
17249648 64 Identification and characterization of 4-methylbenzyl 4-[(pyrimidin-2-ylamino)methyl]piperidine-1-carboxylate, an orally bioavailable, brain penetrant NR2B selective N-methyl-D-aspartate receptor antagonist.EBI Merck Research Laboratories
12639561 51 Orally efficacious NR2B-selective NMDA receptor antagonists.EBI Merck Research Laboratories
12519057 22 3-[(2-Methyl-1,3-thiazol-4-yl)ethynyl]-pyridine: a potent and highly selective metabotropic glutamate subtype 5 receptor antagonist with anxiolytic activity.EBI Merck Research Laboratories
10741546 66 Parallel synthesis of a series of subtype-selective NMDA receptor antagonists.EBI Parke-Davis Pharmaceutical Research
17761421 10 Identification of novel chemical inhibitors for ubiquitin C-terminal hydrolase-L3 by virtual screening.BDB Waseda University
15771420 58 Discovery of 1-(3'-aminobenzisoxazol-5'-yl)-3-trifluoromethyl-N-[2-fluoro-4-[(2'-dimethylaminomethyl)imidazol-1-yl]phenyl]-1H-pyrazole-5-carboxyamide hydrochloride (razaxaban), a highly potent, selective, and orally bioavailable factor Xa inhibitor.BDB Bristol-Myers Squibb Pharmaceutical Research Institute
11881999 123 Novel 4-anilinoquinazolines with C-7 basic side chains: design and structure activity relationship of a series of potent, orally active, VEGF receptor tyrosine kinase inhibitors.BDB Astrazeneca