25 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
26862980	37	Tweaking Subtype Selectivity and Agonist Efficacy at (S)-2-Amino-3-(3-hydroxy-5-methyl-isoxazol-4-yl)propionic acid (AMPA) Receptors in a Small Series of BnTetAMPA Analogues.	University of Copenhagen
26653877	47	Studies on Aryl-Substituted Phenylalanines: Synthesis, Activity, and Different Binding Modes at AMPA Receptors.	University of Copenhagen
24824658	8	Structure-activity relationship studies of N-methylated and N-hydroxylated spider polyamine toxins as inhibitors of ionotropic glutamate receptors.	University of Copenhagen
23320429	48	Structure-activity relationship studies of argiotoxins: selective and potent inhibitors of ionotropic glutamate receptors.	University of Copenhagen
23092360	19	General synthesis ofß-alanine-containing spider polyamine toxins and discovery of nephila polyamine toxins 1 and 8 as highly 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
19588945	55	The glutamate receptor GluR5 agonist (S)-2-amino-3-(3-hydroxy-7,8-dihydro-6H-cyclohepta[d]isoxazol-4-yl)propionic acid and the 8-methyl analogue: synthesis, molecular pharmacology, and biostructural characterization.	University of Copenhagen
18811139	126	1H-cyclopentapyrimidine-2,4(1H,3H)-dione-related ionotropic glutamate receptors ligands. structure-activity relationships and identification of potent and Selective iGluR5 modulators.	European Research Centre For Drug Discovery and Development (Natsyndrugs)
18338843	57	Synthesis and pharmacological characterization at glutamate receptors of the four enantiopure isomers of tricholomic acid.	Universit£
16250647	71	2-n-Butyl-9-methyl-8-[1,2,3]triazol-2-yl-9H-purin-6-ylamine and analogues as A2A adenosine receptor antagonists. Design, synthesis, and pharmacological characterization.	Universit£
9357531	58	Synthesis of willardiine and 6-azawillardiine analogs: pharmacological characterization on cloned homomeric human AMPA and kainate receptor subtypes.	University of Bristol
1977908	10	(R)-4-oxo-5-phosphononorvaline: a new competitive glutamate antagonist at the NMDA receptor complex.	Merrell Dow Research Institute
21923187	5	A new phenylalanine derivative acts as an antagonist at the AMPA receptor GluA2 and introduces partial domain closure: synthesis, resolution, pharmacology, and crystal structure.	University of Copenhagen
21067182	37	Biostructural and Pharmacological Studies of Bicyclic Analogues of the 3-Isoxazolol Glutamate Receptor Agonist Ibotenic Acid	TBA
20684595	374	Quinazolin-4-one derivatives: A novel class of noncompetitive NR2C/D subunit-selective N-methyl-D-aspartate receptor antagonists.	Emory University
20096591	84	Developing a complete pharmacology for AMPA receptors: a perspective on subtype-selective ligands.	University of California
	10	Synthesis and biology of the rigidified glutamate analogue, trans-2-carboxyazetidine-3-acetic acid (t-CAA)	TBA
17455929	36	A tetrazolyl-substituted subtype-selective AMPA receptor agonist.	University of Copenhagen
16942015	43	Uncompetitive antagonism of AMPA receptors: Mechanistic insights from studies of polyamine toxin derivatives.	The Danish University of Pharmaceutical Sciences
15615543	56	Bioisosteric modifications of 2-arylureidobenzoic acids: selective noncompetitive antagonists for the homomeric kainate receptor subtype GluR5.	The Danish University of Pharmaceutical Sciences
12747796	39	Design, synthesis, and pharmacology of a highly subtype-selective GluR1/2 agonist, (RS)-2-amino-3-(4-chloro-3-hydroxy-5-isoxazolyl)propionic acid (Cl-HIBO).	The Danish University of Pharmaceutical Sciences
30943028	66	Use of the 4-Hydroxytriazole Moiety as a Bioisosteric Tool in the Development of Ionotropic Glutamate Receptor Ligands.	University of Turin
7629789	8	Synthesis, resolution, and biological evaluation of the four stereoisomers of 4-methylglutamic acid: selective probes of kainate receptors.	Symphony Pharmaceuticals
30125106	4	Controlling Ca	University of Copenhagen