Taniplon
Chemical compound
- none
- 3-(5-methoxy-6,7,8,9-tetrahydroimidazo[1,2-a]quinazolin-2-yl)-5-methyl-1,2,4-oxadiazole
- 106073-01-2 Y
- 3086516
- 2343126 N
- OKS0I0BBLP
- DTXSID00147500
- Interactive image
- CC1=NC(C2=CN3C(N=C(OC)C4=C3CCCC4)=N2)=NO1
InChI
- 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
Taniplon is a nonbenzodiazepine anxiolytic drug from the imidazoquinazoline family of drugs.
Taniplon binds strongly to benzodiazepine sites on the GABAA receptor and has similar anxiolytic effects in animals, but with less sedative or muscle relaxant action.[1]
References
- ^ 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.
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(α2δ VDCC blockers)
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- #WHO-EM
- ‡Withdrawn from market
- Clinical trials:
- †Phase III
- §Never to phase III