🌐EnglishEnglishDeutschFrançaisItalianoفارسی中文日本語EntityQ756551· pop 11· linked from 456 articlesquisqualic acidAlso known as Quisqualatechemical compoundChemical dataFormulaC5H7N3O5Molecular weight189.13 g/molIUPAC name(2S)-2-azaniumyl-3-(3,5-dioxo-1,2,4-oxadiazolidin-2-yl)propanoatevia PubChemResearch1,568 papersQuisqualic acid-induced neurotoxicity is protected by NMDA and non-NMDA receptor antagonists.Neuroscience letters · 1992Posttraumatic syringomyelia.Journal of neurosurgery. Spine · 2011Quisqualic acid modulates kainate responses in cultured cerebellar granule cells.Journal of neurochemistry · 1989Quisqualic acid analogues: synthesis of beta-heterocyclic 2-aminopropanoic acid derivatives and their activity at a novel quisqualate-sensitized site.Journal of medicinal chemistry · 1992Increased [³H]quisqualic acid binding density in the dorsal striatum and anterior insula of alcoholics: A post-mortem whole-hemisphere autoradiography study.Gallery (2)Available in 10 languagesFrançais中文日本語azbHungarianSerbianSerbian (Latin)Urduفارسیvia Wikidata sitelinks · CC0ConnectionsneurotransmitterEntityDL-glutamic acidEntityCategories2,3-Diaminopropionic acidsAMPA receptor agonistsCarbamatesChembox having GHS dataConvulsantsECHA InfoCard ID from WikidataExcitotoxinsImidesKainate receptor agonistsLactamsMGlu1 receptor agonistsMGlu5 receptor agonistsNeurotoxins