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Taniplon

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Taniplon
Clinical data
ATC code
  • none
Identifiers
  • 3-(5-methoxy-6,7,8,9-tetrahydroimidazo[1,2-a]quinazolin-2-yl)-5-methyl-1,2,4-oxadiazole
CAS Number
PubChemCID
ChemSpider
UNII
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC14H15N5O2
Molar mass285.307 g·mol−1
3D model (JSmol)
  • CC1=NC(C2=CN3C(N=C(OC)C4=C3CCCC4)=N2)=NO1
  • InChI=1S/C14H15N5O2/c1-8-15-12(18-21-8)10-7-19-11-6-4-3-5-9(11)13(20-2)17-14(19)16-10/h7H,3-6H2,1-2H3 ☒N
  • Key:OYKONKGGKFFMDV-UHFFFAOYSA-N ☒N
 ☒NcheckY (what is this?)  (verify)

Taniplon is anonbenzodiazepineanxiolytic drug from theimidazoquinazoline family of drugs.

Taniplon binds strongly to benzodiazepine sites on theGABAAreceptor and has similaranxiolytic effects in animals, but with lesssedative ormuscle relaxant action.[1]

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.
5-HT1ARTooltip 5-HT1A receptoragonists
GABAARTooltip GABAA receptorPAMsTooltip positive allosteric modulators
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Kava constituents
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Nonbenzodiazepines
Phenols
Piperidinediones
Pyrazolopyridines
Quinazolinones
Volatiles/gases
Others/unsorted
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