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Radequinil

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Radequinil
Clinical data
ATC code
  • None
Identifiers
  • 5-(3-methoxyphenyl)-3-(5-methyl-1,2,4-oxadiazol-3-yl)-1,6-naphthyridin-2(1H)-one
CAS Number
PubChemCID
ChemSpider
UNII
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC18H14N4O3
Molar mass334.335 g·mol−1
3D model (JSmol)
  • COc1cccc(c1)c3nccc2NC(=O)\C(=C/c23)c4nc(C)on4
  • InChI=1S/C18H14N4O3/c1-10-20-17(22-25-10)14-9-13-15(21-18(14)23)6-7-19-16(13)11-4-3-5-12(8-11)24-2/h3-9H,1-2H3,(H,21,23)
  • Key:JQOFKKWHXGQABB-UHFFFAOYSA-N

Radequinil (INN;AC-3933) is acognitive enhancer which acts as a partialinverse agonist of thebenzodiazepine site of theGABAA receptor.[1] It was under development byDainippon Sumitomo Pharma for the treatment ofAlzheimer's disease and made it tophase IIclinical trials but development seems to have been halted and it was never marketed.[1][2]

See also

[edit]

References

[edit]
  1. ^abMartocchia A, Falaschi P (2008)."Current Strategies of Therapy in Alzheimer's Disease"(PDF).The Open Neuropsychopharmacology Journal.1:19–23.doi:10.2174/1876523800801010019.
  2. ^Pogacić V, Herrling P (2007)."List of drugs in development for neurodegenerative diseases. Update June 2007".Neuro-Degenerative Diseases.4 (6):443–86.doi:10.1159/000107705.PMID 17934328.
Ionotropic
GABAATooltip γ-Aminobutyric acid A receptor
GABAATooltip γ-Aminobutyric acid A-rho receptor
Metabotropic
GABABTooltip γ-Aminobutyric acid B receptor


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