sym 2081 has been researched along with glutamic acid in 6 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (16.67) | 18.2507 |
| 2000's | 3 (50.00) | 29.6817 |
| 2010's | 2 (33.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Acher, FC; Brabet, I; Jullian, N; Pin, JP | 1 |
| Baker, SR; Ballyk, BA; Bleakman, D; Collado, I; Domínguez, C; Escribano, A; Ezquerra, J; Goldsworthy, J; Hoo, K; Kamboj, RK; Mateo, AI; Pedregal, C; Rubio, A | 1 |
| Alaux, S; Bolte, J; Bräuner-Osborne, H; Bunch, L; Gefflaut, T; Jensen, AA; Kusk, M; Sagot, E | 1 |
| Bolte, J; Bunch, L; Chapelet, M; Gefflaut, T; Nielsen, B; Pickering, DS; Pu, X; Sagot, E; Stensbøl, TB; Umberti, M | 1 |
| Briel, D; Kronbach, C; Rybak, A; Unverferth, K | 1 |
| Amir, A; Brindisi, M; Butini, S; Campiani, G; Coccone, SS; Frydenvang, K; Gemma, S; Guarino, E; Kastrup, JS; Kumar, V; Maramai, S; Novellino, E; Pickering, DS; Valadés, EA; Valenti, S; Venskutonyte, R | 1 |
6 other study(ies) available for sym 2081 and glutamic acid
| Article | Year |
|---|---|
Agonist selectivity of mGluR1 and mGluR2 metabotropic receptors: a different environment but similar recognition of an extended glutamate conformation.
Topics: Animals; Binding Sites; Cell Line; CHO Cells; Cricetinae; Glutamates; Ligands; Models, Molecular; Molecular Conformation; Receptors, Metabotropic Glutamate; Structure-Activity Relationship | 1999 |
4-Alkyl- and 4-cinnamylglutamic acid analogues are potent GluR5 kainate receptor agonists.
Topics: Acetylene; Cell Line; Cells, Cultured; Electrophysiology; Ganglia, Spinal; Glutamates; Humans; Molecular Structure; Neurons; Patch-Clamp Techniques; Receptors, AMPA; Receptors, Kainic Acid; Receptors, N-Methyl-D-Aspartate; Structure-Activity Relationship | 2000 |
Chemoenzymatic synthesis of a series of 4-substituted glutamate analogues and pharmacological characterization at human glutamate transporters subtypes 1-3.
Topics: Animals; Aspartate Aminotransferases; Cell Line; Excitatory Amino Acid Transporter 2; Excitatory Amino Acid Transporter 3; Glutamates; Humans; Ketoglutaric Acids; Membrane Potentials; Models, Molecular; Myocardium; Stereoisomerism; Structure-Activity Relationship; Swine | 2005 |
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.
Topics: Amination; Animals; Glutamic Acid; Magnetic Resonance Spectroscopy; Mass Spectrometry; Rats; Receptors, Glutamate; Spectrophotometry, Infrared; Structure-Activity Relationship; Synaptosomes | 2008 |
Substituted 2-aminothiopen-derivatives: a potential new class of GluR6-antagonists.
Topics: Animals; Cell Line; GluK2 Kainate Receptor; High-Throughput Screening Assays; Humans; Inhibitory Concentration 50; Receptors, Kainic Acid; Substrate Specificity; Thiophenes | 2010 |
Selective kainate receptor (GluK1) ligands structurally based upon 1H-cyclopentapyrimidin-2,4(1H,3H)-dione: synthesis, molecular modeling, and pharmacological and biostructural characterization.
Topics: Animals; Cell Line; Cricetinae; Crystallography, X-Ray; Female; Ligands; Models, Molecular; Oocytes; Patch-Clamp Techniques; Protein Conformation; Pyrimidines; Rats; Receptors, Kainic Acid; Recombinant Proteins; Stereoisomerism; Structure-Activity Relationship; Thiophenes; Xenopus laevis | 2011 |