alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid and (S)-ATPA

alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid has been researched along with (S)-ATPA in 2 studies

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Bräuner-Osborne, H; Brehm, L; Egebjerg, J; Greenwood, JR; Hansen, KB; Krogsgaard-Larsen, P; Kronborg, TT; Nielsen, B; Sløk, FA; Stensbøl, TB1
Bräuner-Osborne, H; Brehm, L; Clausen, RP; Gajhede, M; Geneser, U; Greenwood, JR; Jensen, AA; Kastrup, JS; Kristensen, AS; Krogsgaard-Larsen, P; Naur, P; Nielsen, AS; Nielsen, B; Pickering, DS; Ringgaard, LM; Strange, M1

Other Studies

2 other study(ies) available for alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid and (S)-ATPA

ArticleYear
(S)-2-Amino-3-(3-hydroxy-7,8-dihydro-6H-cyclohepta[d]isoxazol-4-yl)propionic acid, a potent and selective agonist at the GluR5 subtype of ionotropic glutamate receptors. Synthesis, modeling, and molecular pharmacology.
    Journal of medicinal chemistry, 2003, Apr-10, Volume: 46, Issue:8

    Topics: Alanine; Amino Acid Sequence; Animals; CHO Cells; Cricetinae; Excitatory Amino Acid Agonists; In Vitro Techniques; Isoxazoles; Ligands; Models, Molecular; Molecular Conformation; Molecular Sequence Data; Monte Carlo Method; Oocytes; Patch-Clamp Techniques; Propionates; Radioligand Assay; Receptors, Kainic Acid; Sequence Homology, Amino Acid; Stereoisomerism; Structure-Activity Relationship; Xenopus laevis

2003
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.
    Journal of medicinal chemistry, 2009, Aug-13, Volume: 52, Issue:15

    Topics: Animals; Cell Line; Crystallography, X-Ray; Drug Design; Excitatory Amino Acid Agonists; Humans; Models, Molecular; Propionates; Receptors, Kainic Acid; Stereoisomerism; Structure-Activity Relationship; Xenopus laevis

2009