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Spiramide

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Spiramide
Clinical data
ATC code
  • none
Identifiers
  • 8-[3-(4-Fluorophenoxy)propyl]-1-phenyl-1,3,8-triazaspiro[4,5]decan-4-one
CAS Number
PubChemCID
IUPHAR/BPS
ChemSpider
UNII
ChEBI
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC22H27FN3O2
Molar mass384.475g·mol−1
3D model (JSmol)
  • c2cc(F)ccc2OCCCN3CCC1(CC3)N(CNC1=O)c4ccccc4
  • InChI=1S/C22H26FN3O2/c23-18-7-9-20(10-8-18)28-16-4-13-25-14-11-22(12-15-25)21(27)24-17-26(22)19-5-2-1-3-6-19/h1-3,5-10H,4,11-17H2,(H,24,27)
  • Key:FJUKDAZEABGEIH-UHFFFAOYSA-N
(verify)

Spiramide(developmental code nameAMI-193) is an experimentalantipsychoticthat acts as aselective5-HT2A,5-HT1A,andD2receptorantagonist.It has negligibleaffinityfor the5-HT2Creceptor.[1][2][3]

References

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  1. ^Czoty PW, Howell LL (October 2000). "Behavioral effects of AMI-193, a 5-HT(2A)- and dopamine D(2)-receptor antagonist, in the squirrel monkey".Pharmacology Biochemistry and Behavior.67(2): 257–64.doi:10.1016/S0091-3057(00)00321-X.PMID11124389.S2CID36132685.
  2. ^Luparini MR, Garrone B, Pazzagli M, Pinza M, Pepeu G (November 2004)."A cortical GABA-5HT interaction in the mechanism of action of the antidepressant trazodone".Progress in Neuro-psychopharmacology & Biological Psychiatry.28(7): 1117–27.doi:10.1016/j.pnpbp.2004.05.046.PMID15610924.S2CID24076522.
  3. ^Hamada K, Yoshida M, Isayama H, Yagi Y, Kanazashi S, Kashihara Y, Takeuchi K, Yamaguchi I (November 2007)."Possible involvement of endogenous 5-HT in aggravation of cerulein-induced acute pancreatitis in mice".Journal of Pharmacological Sciences.105(3): 240–50.doi:10.1254/jphs.FP0071049.PMID17965538.