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Summary Anatomy Item Literature (1850) Expression Attributions Wiki
XB-ANAT-16

Papers associated with hindbrain (and grik1)

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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., Clausen RP., J Med Chem. August 13, 2009; 52 (15): 4911-22.

Tetrazolyl isoxazole amino acids as ionotropic glutamate receptor antagonists: synthesis, modelling and molecular pharmacology., Frølund B., Bioorg Med Chem. September 15, 2005; 13 (18): 5391-8.

(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., Brehm L., J Med Chem. April 10, 2003; 46 (8): 1350-8.

Stereochemistry and molecular pharmacology of (S)-thio-ATPA, a new potent and selective GluR5 agonist., Stensbøl TB., Eur J Pharmacol. January 12, 2001; 411 (3): 245-53.

Resolution, configurational assignment, and enantiopharmacology of 2-amino-3-[3-hydroxy-5-(2-methyl-2H- tetrazol-5-yl)isoxazol-4-yl]propionic acid, a potent GluR3- and GluR4-preferring AMPA receptor agonist., Vogensen SB., Chirality. November 1, 2000; 12 (10): 705-13.

Resolution, absolute stereochemistry and molecular pharmacology of the enantiomers of ATPA., Stensbøl TB., Eur J Pharmacol. September 10, 1999; 380 (2-3): 153-62.

Resolution, absolute stereochemistry, and enantiopharmacology of the GluR1-4 and GluR5 antagonist 2-amino-3-[5-tert-butyl-3-(phosphonomethoxy)-4-isoxazolyl]propionic acid., Møller EH., Chirality. January 1, 1999; 11 (10): 752-9.

Antagonist properties of a phosphono isoxazole amino acid at glutamate R1-4 (R,S)-2-amino-3-(3-hydroxy-5-methyl-4-isoxazolyl)propionic acid receptor subtypes., Wahl P., Mol Pharmacol. March 1, 1998; 53 (3): 590-6.

Pharmacology and toxicology of ATOA, an AMPA receptor antagonist and a partial agonist at GluR5 receptors., Wahl P., Neuropharmacology. January 1, 1998; 37 (10-11): 1205-10.

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