Cloperidone
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Formula | C21H23ClN4O2 |
Molar mass | 398.89 g·mol−1 |
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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
[edit]- ^ 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.
- ^ a b c "Cloperidone hydrochloride". Inxight Drugs. NCATS. Retrieved 8 June 2025.