Haloperidol (hydrochloride) structure
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Common Name | Haloperidol (hydrochloride) | ||
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CAS Number | 1511-16-6 | Molecular Weight | 412.32500 | |
Density | N/A | Boiling Point | N/A | |
Molecular Formula | C21H24Cl2FNO2 | Melting Point | N/A | |
MSDS | N/A | Flash Point | N/A |
Use of Haloperidol (hydrochloride)Haloperidol hydrochloride is a potent dopamine D2 receptor antagonist, widely used as an antipsychotic. |
Name | 4-[4-(4-chlorophenyl)-4-hydroxypiperidin-1-yl]-1-(4-fluorophenyl)butan-1-one,hydrochloride |
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Synonym | More Synonyms |
Description | Haloperidol hydrochloride is a potent dopamine D2 receptor antagonist, widely used as an antipsychotic. |
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Related Catalog | |
In Vivo | Haloperidol (1 mg) intra-arterially attenuates the dopamine-induced pancreatic secretion. Haloperidol (3 mg) completely inhibits the action of 10 μg of dopamine in the pancreas of the dogs[1]. Haloperidol (10 mg/kg) as well as chlorpromazine (CPZ, 15 mg/kg) blocks mescaline-induced altered behavior within 7 to 10 minutes when injected into the mice 45 minutes after 50 mg/kg (2 µc) of mescaline. Haloperidol has no effect on mescaline disappearance[2]. |
Animal Admin | Male albino mice of Swiss-Webster strain (33-36 g) are used, and all substances are given by i.p. injection in a volume of 0.5 mL. CPZ, haloperidoi and mescaline are all in time form of timeir imydrochlorides and the dose solutions are prepared at concentrations of 1.0, 0.66 and 3.3 mg/mL of 0.9% saline, respectively. The doses are: CPZ, 15 mg/kg; haloperidol, 10 mg/kg; mescaline, 50 mg/kg. Mice are pretreated with either CPZ or haloperidol 30 minutes before administration of mescaline. In some instances CPZ is injected 45 minutes after mescaline. Time animals are hmoused individually in a plexiglas cage and the gross behavior and locomotor activity. At selected intervals after mescaline, groups of mice are sacrificed by decapitation. Plasma is separated and stored at -20°C. The brain, liver, kidney, lung, spleen and heart are frozen on dry ice and stored at -20°C for 18 to 20 hours before they are used for assays. |
References |
Molecular Formula | C21H24Cl2FNO2 |
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Molecular Weight | 412.32500 |
Exact Mass | 411.11700 |
PSA | 40.54000 |
LogP | 5.16550 |
Storage condition | 2-8℃ |
4-[4-(4-chlorophenyl)-4-hydroxypiperidino]-4'-fluorobutyrophenone hydrochloride |
4-[4-(4-Chlor-phenyl)-4-hydroxy-piperidino]-1-(4-fluor-phenyl)-butan-1-on,Hydrochlorid |
Haloperidol chlorohydrate |
Haloperidol hydrochloride [MI] |
UNII-UM06W2ADRY |
4-[4-(4-chloro-phenyl)-4-hydroxy-piperidino]-1-(4-fluoro-phenyl)-butan-1-one,hydrochloride |
Haloperidol hydrochloride |
Haloperidol chloride |
Haloperidol (hydrochloride) |