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Fasiplon

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Fasiplon
Clinical data
ATC code
  • none
Identifiers
  • 6-Ethyl-7-methoxy-5-methyl-2-(5-methyl-[1,2,4]oxadiazol-3-yl)-imidazo[1,2-a]pyrimidine
CAS Number
PubChemCID
ChemSpider
UNII
ChEMBL
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC13H15N5O2
Molar mass273.296 g·mol−1
3D model (JSmol)
  • CC1=NC(C2=CN3C(N=C(OC)C(CC)=C3C)=N2)=NO1
  • InChI=1S/C13H15N5O2/c1-5-9-7(2)18-6-10(11-14-8(3)20-17-11)15-13(18)16-12(9)19-4/h6H,5H2,1-4H3 ☒N
  • Key:MEBYKPLMXIRYRQ-UHFFFAOYSA-N ☒N
 ☒NcheckY (what is this?)  (verify)

Fasiplon (RU 33203) is anonbenzodiazepineanxiolytic drug from theimidazopyrimidine family of drugs.

Fasiplon binds strongly to benzodiazepine sites on theGABAAreceptor and has similaranxiolytic effects in animals, but with lesssedative ormuscle relaxant action.[1] It was developed by a team atRoussel Uclaf in the 1990s[2]

References

[edit]
  1. ^Tully WR, Gardner CR, Gillespie RJ, Westwood R (July 1991). "2-(oxadiazolyl)- and 2-(thiazolyl)imidazo[1,2-a]pyrimidines as agonists and inverse agonists at benzodiazepine receptors".Journal of Medicinal Chemistry.34 (7):2060–7.doi:10.1021/jm00111a021.PMID 1648620.
  2. ^US Patent 5869481 Anticonvulsive 1-ar(alk)ylimidazolin-2-ones and process for making
5-HT1ARTooltip 5-HT1A receptoragonists
GABAARTooltip GABAA receptorPAMsTooltip positive allosteric modulators
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