物质信息

ID:385

名称和标识
商标名
AloperidolAloperidonHaldolHalojustHaloperidol IntensolPelucesHalostenPekucesPeridolSernasDozicEinalon SHaldol SolutabHaloperidol LactateHalopoidolKeselanLintonMixidolNovo-PeridolApo-HaloperidolBrotoponEukystolHalidolHalolHalopalUlcolindUliolindALDOAloperidinHalopidolLealgin CompositumPernoxPms HaloperidolSerenaceSigaperidolDozixGaloperidolHaldol DecanoateHaldol LaHaloperidoHaloperidol DecanoateSerenaseSerenelfiSernelVesaliumAloperidoloBioperidolo
IUPAC传统名
haloperidol
IUPAC标准名
4-[4-(4-chlorophenyl)-4-hydroxypiperidin-1-yl]-1-(4-fluorophenyl)butan-1-one
别名
Haloperidol
数据登录号
PubChem CID
CAS号
PubChem SID
化合物性质
理化性质
疏水性(logP)
4
溶解度
14 mg/L
描述信息
Drug Groups
approved
Description
A phenyl-piperidinyl-butyrophenone that is used primarily to treat schizophrenia and other psychoses. It is also used in schizoaffective disorder, delusional disorders, ballism, and tourette syndrome (a drug of choice) and occasionally as adjunctive therapy in mental retardation and the chorea of huntington disease. It is a potent antiemetic and is used in the treatment of intractable hiccups. (From AMA Drug Evaluations Annual, 1994, p279)
Indication
For the management of psychotic disorders (eg. schizophrenia) and delirium, as well as to control tics and vocal utterances of Tourette's syndrome (Gilles de la Tourette's syndrome). Also used for the treatment of severe behavioural problems in children with disrubtive behaviour disorder or ADHD (attention-deficit hyperactivity disorder). Haloperidol has been used in the prevention and control of severe nausea and vomiting.
Pharmacology
Haloperidol is a psychotropic agent indicated for the treatment of schizophrenia. It also exerts sedative and antiemetic activity. Haloperidol principal pharmacological effects are similar to those of piperazine-derivative phenothiazines. The drug has action at all levels of the central nervous system-primarily at subcortical levels-as well as on multiple organ systems. Haloperidol has strong antiadrenergic and weaker peripheral anticholinergic activity; ganglionic blocking action is relatively slight. It also possesses slight antihistaminic and antiserotonin activity.
Toxicity
LD50=165 mg/kg (rats, oral)
Affected Organisms
Humans and other mammals
Biotransformation
Hepatic
Absorption
Oral-60%
Half Life
3 weeks
Protein Binding
92%
References
• Niemegeers CJ, Laduron PM: Pharmacology and biochemistry of haloperidol. Proc R Soc Med. 1976;69 suppl 1:3-8. [Pubmed]
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参考文献
• Niemegeers CJ, Laduron PM: Pharmacology and biochemistry of haloperidol. Proc R Soc Med. 1976;69 suppl 1:3-8. Pubmed