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L-Quisqualic acid is a natural analog of glutamate that acts as an agonist at AMPA-selective and metabotropic glutamate receptors (EC50s = 170, 10, 40, and 29 nM at GluR-A, mGluR1, mGluR3, and mGluR5, respectively), as well as the ionotropic kainate receptor (GRIK4; Ki = 6.43 nM).1,2,3,4,5,6 L-Quisqualic acid is used to study receptor dynamics and as an excitotoxin to selectively destroy neurons in the brain or spinal cord.7,8
WARNING This product is not for human or veterinary use.
1. Pharmacological agents acting at subtypes of metabotropic glutamate receptors. Neuropharmacology 38(10), 1431-1476 (1999).
2. Ligands for glutamate receptors: Design and therapeutic prospects. J. Med. Chem. 43(14), 2609-2645 (2000).
3. Common and selective molecular determinants involved in metabotopic glutamate receptor agonist activity. J. Med. Chem. 45(15), 3171-3183 (2002).
4. Molecular cloning, expression, and pharmacological characterization of humEAA1, a human kainate receptor subunit. J.Neurochem. 62(1), 1-9 (1994).
5. Characterization of [3H]quisqualate binding to recombinant rat metabotropic glutamate 1a and 5a receptors and to rat and human brain sections. J. Neurochem. 75(6), 2590-2601 (2000).
6. Mutations in a putative agonist binding region of the AMPA-
7. Prolonged nociceptive responses to hind paw formalin injection in rats with a spinal cord injury. Neurosci. Lett. 439(2), 212-215 (2008).
8. Excitotoxic lesions of basal forebrain cholinergic neurons: effects on learning, memory and attention. Behav. Brain Res. 57(2), 123-131 (1993).