Cloperidone
Cas number4052-13-5
Pubchem10675
Chemspiderid10225
Unii8FP5Y6U39R
Chembl2110792
Iupac name3-[3-[4-(3-chlorophenyl)piperazin-1-yl]propyl]-1H-quinazoline-2,4-dione
C21
H23
Cl1
N4
O2
SmilesC1CN(CCN1CCCN2C(=O)C3=CC=CC=C3NC2=O)C4=CC(=CC=C4)Cl
Stdinchi1S/C21H23ClN4O2/c22-16-5-3-6-17(15-16)25-13-11-24(12-14-25)9-4-10-26-20(27)18-7-1-2-8-19(18)23-21(26)28/h1-3,5-8,15H,4,9-14H2,(H,23,28)
StdinchikeyFXZJKVODWNYPKK-UHFFFAOYSA-N

Cloperidone is a quinazolinedione derivative first reported in 1965 by Miles Laboratories, notable for its sedative and antihypertensive properties.[1][2] Its pharmacological activity has been demonstrated in various animal models, including behavioral studies in dogs and cats, as well as motor coordination and locomotor activity assays in mice.[2] Cloperidone is not an approved drug and appears to remain an experimental compound with no current clinical use.[2]

References

  1. ^ Hayao S, Havera HJ, Strycker WG, Leipzig TJ, Kulp RA, Hartzler HE (November 1965). "New sedative and hypotensive 3-substituted 2,4(1H,3H)-quinazolinediones". Journal of Medicinal Chemistry. 8 (6): 807–815. doi:10.1021/jm00330a017. PMID 5885076
  2. ^ "Cloperidone hydrochloride". Inxight Drugs. NCATS. Retrieved 8 June 2025.