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Images L-Quisqualic acid product vial image | Hello Bio
L-Quisqualic acid product vial image | Hello Bio Biological Data Biological description AMPA receptor agonist and group I mGlu agonist. Sensitizes hippocampal neurons to depolarization by excitatory amino acid analogues such as L-AP4 , and L-AP6 ("the Quis effect"). Can also act as an excitotoxin and is used to lesion areas of the brain in rat models.
Solubility & Handling Storage instructions Room temperature
Solubility overview Soluble in NaOH(aq) (100mM, 1eq. NaOH) or water (10mM)
Important This product is for RESEARCH USE ONLY and is not intended for therapeutic or diagnostic use. Not for human or veterinary use.
Chemical Data Chemical name (L)-(+)-α-Amino-3,5-dioxo-1,2,4-oxadiazolidine-2-propanoic acid
Chemical structure
Molecular Formula C5 H7 N3 O5
SMILES O=C1N(C[C@]([H])(N)C(O)=O)OC(N1)=O
InChi InChI=1S/C5H7N3O5/c6-2(3(9)10)1-8-4(11)7-5(12)13-8/h2H,1,6H2,(H,9,10)(H,7,11,12)/t2-/m0/s1
InChiKey ASNFTDCKZKHJSW-REOHCLBHSA-N
References for L-Quisqualic acid References are publications that support the biological activity of the product
Prolonged nociceptive responses to hind paw formalin injection in rats with a spinal cord injury. Lee JW et al (2008) Neurosci Lett 439(2) : 212-5. L-Quisqualic acid transport into hippocampal neurons by a cystine-sensitive carrier is required for the induction of quisqualate sensitization. Chase LA et al (2001) Neuroscience 106(2) : 287-301. C-fos expression in the rat nucleus basalis upon excitotoxic lesion with quisqualic acid: a study in adult and aged animals. Giovannelli L et al (1998) J Neural Transm 105(8-9) : 935-48. Effects of quisqualic acid analogs on metabotropic glutamate receptors coupled to phosphoinositide hydrolysis in rat hippocampus. Littman L et al (1995) Neuropharmacology 34(8) : 829-41.
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AMPA receptor agonist and group I mGlu agonist