Drug intelligence / Profile preview

haloperidol

Development stage
Approved
Lead developer
Johnson & Johnson
Modality
Small Molecules
Administration
Oral, Intramuscular, Intravenous
01

Overview

Haloperidol is a first-generation (typical) antipsychotic of the butyrophenone class, primarily used to treat schizophrenia, acute psychosis, and tics associated with Tourette's syndrome. It is also indicated for severe behavioral problems in children and for managing agitation, delirium, and mania. Haloperidol acts mainly as a potent antagonist of dopamine D2 receptors in the brain, reducing abnormal excitement and psychotic symptoms. It can be administered orally or by intramuscular/intravenous injection; long-lasting decanoate formulations are available for monthly administration. The drug was developed by Paul Janssen's team in Belgium in 1958 and remains on the WHO Model List of Essential Medicines[1][6][7].

Brand names
HaldolSerenaceAloperidinDozicPernox
Other names
氟哌啶醇 (Chinese)Haloperidolumγ-(4-(p-chlorophenyl)-4-hydroxypiperidino)-p-fluorbutyrophenone1-(3-p-fluorobenzoylpropyl)-4-p-chlorophenyl-4-hydroxypiperidine
02

Targets

DRD2 (Dopamine D2 Receptor)

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