The following articles (labelled with PubMed ID or TBD) are for your review
PMID | Data | Article Title | Organization |
28005385 |
98 |
Design and Synthesis of a Series of l-trans-4-Substituted Prolines as Selective Antagonists for the Ionotropic Glutamate Receptors Including Functional and X-ray Crystallographic Studies of New Subtype Selective Kainic Acid Receptor Subtype 1 (GluK1) Antagonist (2S,4R)-4-(2-Carboxyphenoxy)pyrrolidin |
Mcgill University |
27765511 |
36 |
Design, synthesis and structure-activity relationships of novel phenylalanine-based amino acids as kainate receptors ligands. |
Jagiellonian University Medical College |
26653877 |
47 |
Studies on Aryl-Substituted Phenylalanines: Synthesis, Activity, and Different Binding Modes at AMPA Receptors. |
University of Copenhagen |
25172149 |
36 |
Design, synthesis and in vitro pharmacology of GluK1 and GluK3 antagonists. Studies towards the design of subtype-selective antagonists through 2-carboxyethyl-phenylalanines with substituents interacting with non-conserved residues in the GluK binding sites. |
University of Copenhagen |
23414088 |
102 |
Chemoenzymatic synthesis of new 2,4-syn-functionalized (S)-glutamate analogues and structure-activity relationship studies at ionotropic glutamate receptors and excitatory amino acid transporters. |
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 |
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£ |
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) |
18578478 |
60 |
Chemo-enzymatic synthesis of a series of 2,4-syn-functionalized (S)-glutamate analogues: new insight into the structure-activity relation of ionotropic glutamate receptor subtypes 5, 6, and 7. |
Universite Blaise Pascal |
18578477 |
77 |
Chemo-enzymatic synthesis of (2S,4R)-2-amino-4-(3-(2,2-diphenylethylamino)-3-oxopropyl)pentanedioic acid: a novel selective inhibitor of human excitatory amino acid transporter subtype 2. |
Universite Blaise Pascal |
18338843 |
57 |
Synthesis and pharmacological characterization at glutamate receptors of the four enantiopure isomers of tricholomic acid. |
Universit£ |
17348638 |
25 |
Synthesis and pharmacological characterization of N3-substituted willardiine derivatives: role of the substituent at the 5-position of the uracil ring in the development of highly potent and selective GLUK5 kainate receptor antagonists. |
University Walk |
16302825 |
33 |
Synthesis and pharmacology of willardiine derivatives acting as antagonists of kainate receptors. |
University Walk |
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£ |
10969973 |
103 |
4-Alkylidenyl glutamic acids, potent and selective GluR5 agonists. |
Eli Lilly |
21619066 |
41 |
Selective kainate receptor (GluK1) ligands structurally based upon 1H-cyclopentapyrimidin-2,4(1H,3H)-dione: synthesis, molecular modeling, and pharmacological and biostructural characterization. |
University of Copenhagen |
21067182 |
37 |
Biostructural and Pharmacological Studies of Bicyclic Analogues of the 3-Isoxazolol Glutamate Receptor Agonist Ibotenic Acid |
TBA |
19656686 |
20 |
3-Substituted phenylalanines as selective AMPA- and kainate receptor ligands. |
University of Copenhagen |
17455929 |
36 |
A tetrazolyl-substituted subtype-selective AMPA receptor agonist. |
University of Copenhagen |
16216501 |
1 |
New 7,8-ethylenedioxy-2,3-benzodiazepines as noncompetitive AMPA receptor antagonists. |
Università |
11831912 |
43 |
Selective antagonists at group I metabotropic glutamate receptors: synthesis and molecular pharmacology of 4-aryl-3-isoxazolol amino acids. |
The Royal Danish School of Pharmacy |
29451794 |
20 |
( S)-2-Amino-3-(5-methyl-3-hydroxyisoxazol-4-yl)propanoic Acid (AMPA) and Kainate Receptor Ligands: Further Exploration of Bioisosteric Replacements and Structural and Biological Investigation. |
University of Siena |
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 |
26691755 |
19 |
Identifying New Drug Targets for Potent Phospholipase D Inhibitors: Combining Sequence Alignment, Molecular Docking, and Enzyme Activity/Binding Assays. |
Roxbury Community College |