29 articles for thisTarget

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The following articles (labelled with PubMed ID or TBD) are for your review

PMID	Data	Article Title	Organization
28222314	3	Systematic variation of the benzenesulfonamide part of the GluN2A selective NMDA receptor antagonist TCN-201.	University of M£Nster
27064517	12	Neurosteroid-like Inhibitors of N-Methyl-d-aspartate Receptor: Substituted 2-Sulfates and 2-Hemisuccinates of Perhydrophenanthrene.	Academy of Sciences of The Czech Republic
26525866	7	A novel class of negative allosteric modulators of NMDA receptor function.	Emory University
24824658	8	Structure-activity relationship studies of N-methylated and N-hydroxylated spider polyamine toxins as inhibitors of ionotropic glutamate receptors.	University of Copenhagen
24512267	41	Design, synthesis, and structure-activity relationship of a novel series of GluN2C-selective potentiators.	Emory University
23614571	20	Development of 2'-substituted (2S,1'R,2'S)-2-(carboxycyclopropyl)glycine analogues as potent N-methyl-d-aspartic acid receptor agonists.	University of Copenhagen
23320429	48	Structure-activity relationship studies of argiotoxins: selective and potent inhibitors of ionotropic glutamate receptors.	University of Copenhagen
21188966	2	Solid-phase synthesis and biological evaluation of Joro spider toxin-4 from Nephila clavata.	University of Copenhagen
20408529	32	4-hydroxy-1,2,5-oxadiazol-3-yl moiety as bioisoster of the carboxy function. Synthesis, ionization constants, and molecular pharmacological characterization at ionotropic glutamate receptors of compounds related to glutamate and its homologues.	Universit£
10715162	59	Synthesis of N-substituted 4-(4-hydroxyphenyl)piperidines, 4-(4-hydroxybenzyl)piperidines, and (+/-)-3-(4-hydroxyphenyl)pyrrolidines: selective antagonists at the 1A/2B NMDA receptor subtype.	Cocensys
9719603	39	Structure-activity relationships for a series of bis(phenylalkyl)amines: potent subtype-selective inhibitors of N-methyl-D-aspartate receptors.	University of Oregon
22111545	80	Piperazine-2,3-dicarboxylic acid derivatives as dual antagonists of NMDA and GluK1-containing kainate receptors.	University of Bristol
20684595	374	Quinazolin-4-one derivatives: A novel class of noncompetitive NR2C/D subunit-selective N-methyl-D-aspartate receptor antagonists.	Emory University
19648014	11	Synthesis, structural activity-relationships, and biological evaluation of novel amide-based allosteric binding site antagonists in NR1A/NR2B N-methyl-D-aspartate receptors.	Emory University
17985859	16	Design and synthesis of indole-based peptoids as potent noncompetitive antagonists of transient receptor potential vanilloid 1.	University of Barcelona
15837299	11	NMDA-NR2B subtype selectivity of stereoisomeric 2-(1,2,3,4-tetrahydro-1-isoquinolyl)ethanol derivatives.	Ludwig-Maximilians-UniversitäT MüNchen
15801853	62	Synthesis and pharmacology of N1-substituted piperazine-2,3-dicarboxylic acid derivatives acting as NMDA receptor antagonists.	University Walk
30622023	39	Investigation of the structural requirements for N-methyl-D-aspartate receptor positive and negative allosteric modulators based on 2-naphthoic acid.	University of Bristol
31390523	56	Neuroactive Steroid	Sage Therapeutics
10464027	118	Structure-activity relationship of N-(phenylalkyl)cinnamides as novel NR2B subtype-selective NMDA receptor antagonists.	University of Oregon
10425109	24	4-Hydroxy-1-[2-(4-hydroxyphenoxy)ethyl]-4-(4-methylbenzyl)piperidine: a novel, potent, and selective NR1/2B NMDA receptor antagonist.	Cocensys
10395488	114	Subtype-selective N-methyl-D-aspartate receptor antagonists: synthesis and biological evaluation of 1-(arylalkynyl)-4-benzylpiperidines.	Cocensys
30891121	26	Di-aryl Sulfonamide Motif Adds ?-Stacking Bulk in Negative Allosteric Modulators of the NMDA Receptor.	Emory University
29708744	27	Positive Modulators of the N-Methyl-d-aspartate Receptor: Structure-Activity Relationship Study of Steroidal 3-Hemiesters.	Institute of Physiology of The Czech Academy of Sciences
30125106	4	Controlling Ca	University of Copenhagen
29277306	6	Design, synthesis, and evaluation of polyamine-memantine hybrids as NMDA channel blockers.	Hiroshima University
29397723	267	Increased Potency and Selectivity for Group III Metabotropic Glutamate Receptor Agonists Binding at Dual sites.	University of Paris
29205034	39	Augmentation of Anticancer Drug Efficacy in Murine Hepatocellular Carcinoma Cells by a Peripherally Acting Competitive N-Methyl-d-aspartate (NMDA) Receptor Antagonist.	University of Eastern Finland