Utilization of the resolvedl-isomer of 2-amino-6-phosphonohexanoic acid (l-AP6) as a selective agonist for a quisqualate-sensitized site in hippocampal CA1 pyramidal neurons

This publication has 20 references indexed in Scilit:

• Quisqualic acid analogs: synthesis of .beta.-heterocyclic 2-aminopropanoic acid derivatives and their activity at a novel quisqualate-sensitized site
  Journal of Medicinal Chemistry, 1992
• Molecular Diversity of Glutamate Receptors and Implications for Brain Function
  Science, 1992
• Agonists selective for phosphoinositide-coupled receptors sensitize neurons to depolarization by l-2-amino-4-phosphonobutanoic acid (l-AP4)
  Brain Research, 1991
• N‐Methyl‐D‐Aspartate Receptor Activation and Ca²⁺ Account for Poor Pyramidal Cell Structure in Hippocampal Slices
  Journal of Neurochemistry, 1990
• Novel recognition site forl-quisqualate sensitizes neurons to depolarization byl-2-amino-4-phosphonobutanoate (l-AP4)
  Brain Research, 1989
• The Excitatory Amino Acid Receptors: Their Classes, Pharmacology, and Distinct Properties in the Function of the Central Nervous System
  Annual Review of Pharmacology and Toxicology, 1989
• CNQX blocks acidic amino acid induced depolarizations and synaptic components mediated by non-NMDA receptors in rat hippocampal slices
  Neuroscience Letters, 1988
• Structure - function relationships for gamma-substituted glutamate analogues on dentate granule cells
  Brain Research, 1983
• Micromolar L-2-amino-4-phosphonobutyric acid selectively inhibits perforant path synapses from lateral entorhinal cortex
  Brain Research, 1981
• New class of glutamate agonist structurally related to ibotenic acid
  Nature, 1980