Matches in DBpedia 2016-04 for { <http://wikidata.dbpedia.org/resource/Q7272628> ?p ?o }
Showing triples 1 to 53 of
53
with 100 triples per page.
- Q7272628 subject Q18924463.
- Q7272628 subject Q20870732.
- Q7272628 subject Q7108202.
- Q7272628 subject Q8707578.
- Q7272628 subject Q8788974.
- Q7272628 subject Q8878420.
- Q7272628 subject Q8971959.
- Q7272628 abstract "Quisqualamine is the α-decarboxylated analogue of quisqualic acid, as well as a relative of the neurotransmitters glutamate and γ-aminobutyric acid (GABA). α-Decarboxylation of excitatory amino acids can produce derivatives with inhibitory effects. Indeed, unlike quisqualic acid, quisqualamine has central depressant and neuroprotective properties and appears to act predominantly as an agonist of the GABAA receptor and also to a lesser extent as an agonist of the glycine receptor, due to the facts that its actions are inhibited in vitro by GABAA antagonists like bicuculline and picrotoxin and by the glycine antagonist strychnine, respectively. Mg2+ and DL-AP5, NMDA receptor blockers, CNQX, an antagonist of both the AMPA and kainate receptors, and 2-hydroxysaclofen, a GABAB receptor antagonist, do not affect quisqualamine's actions in vitro, suggesting that it does not directly affect the ionotropic glutamate receptors or the GABAB receptor in any way. Whether it binds to and acts upon any of the metabotropic glutamate receptors like its analogue quisqualic acid however is unclear.".
- Q7272628 iupacName "2-(2-aminoethyl)-1,2,4-oxadiazolidine-3,5-dione".
- Q7272628 thumbnail Quisqualamine.svg?width=300.
- Q7272628 wikiPageWikiLink Q1185869.
- Q7272628 wikiPageWikiLink Q12745592.
- Q7272628 wikiPageWikiLink Q162657.
- Q7272628 wikiPageWikiLink Q181136.
- Q7272628 wikiPageWikiLink Q18924463.
- Q7272628 wikiPageWikiLink Q194406.
- Q7272628 wikiPageWikiLink Q1976211.
- Q7272628 wikiPageWikiLink Q1981368.
- Q7272628 wikiPageWikiLink Q2033959.
- Q7272628 wikiPageWikiLink Q20870732.
- Q7272628 wikiPageWikiLink Q210021.
- Q7272628 wikiPageWikiLink Q221681.
- Q7272628 wikiPageWikiLink Q295251.
- Q7272628 wikiPageWikiLink Q305671.
- Q7272628 wikiPageWikiLink Q3454536.
- Q7272628 wikiPageWikiLink Q3639734.
- Q7272628 wikiPageWikiLink Q389934.
- Q7272628 wikiPageWikiLink Q410943.
- Q7272628 wikiPageWikiLink Q414896.
- Q7272628 wikiPageWikiLink Q416602.
- Q7272628 wikiPageWikiLink Q426887.
- Q7272628 wikiPageWikiLink Q4386534.
- Q7272628 wikiPageWikiLink Q485014.
- Q7272628 wikiPageWikiLink Q5072487.
- Q7272628 wikiPageWikiLink Q60147.
- Q7272628 wikiPageWikiLink Q620730.
- Q7272628 wikiPageWikiLink Q660.
- Q7272628 wikiPageWikiLink Q7108202.
- Q7272628 wikiPageWikiLink Q756551.
- Q7272628 wikiPageWikiLink Q8707578.
- Q7272628 wikiPageWikiLink Q8788974.
- Q7272628 wikiPageWikiLink Q8878420.
- Q7272628 wikiPageWikiLink Q8971959.
- Q7272628 wikiPageWikiLink Q898436.
- Q7272628 iupacname "2".
- Q7272628 type ChemicalCompound.
- Q7272628 type ChemicalSubstance.
- Q7272628 type ChemicalObject.
- Q7272628 type Thing.
- Q7272628 type Q11173.
- Q7272628 comment "Quisqualamine is the α-decarboxylated analogue of quisqualic acid, as well as a relative of the neurotransmitters glutamate and γ-aminobutyric acid (GABA). α-Decarboxylation of excitatory amino acids can produce derivatives with inhibitory effects.".
- Q7272628 label "Quisqualamine".
- Q7272628 depiction Quisqualamine.svg.