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Prochlorperazine

Catalog No. DB00433 Name DrugBank
CAS Number 58-38-8 Website http://www.ualberta.ca/
M. F. C20H24ClN3S Telephone (780) 492-3111
M. W. 373.94266 Fax (780) 492-1071
Purity Email david.wishart@ualberta.ca
Storage Chembase ID: 316

SYNONYMS

IUPAC name
2-chloro-10-[3-(4-methylpiperazin-1-yl)propyl]-10H-phenothiazine
IUPAC Traditional name
prochlorperazine
Brand Name
Emelent
Nipodal
Buccastem
Tementil
Capazine
Bayer A 173
Compro
Eskatrol
Kronocin
Meterazine
Novamin
Temetid
Compazine
Combid
Emetiral
Meterazin
Meterazin Maleate
Pasotomin
Stemetil
Vertigon
Synonyms
Proclorperazine
Prochloroperazine
Prochlorperazin
Prochlorpemazine
Chlormeprazine
Prochlorpromazine
Prochlorperazine maleate
Prochlorperazine edisylate
Procloperazine
Chlorperazine

DATABASE IDS

PubChem CID 4917
CAS Number 58-38-8
PubChem SID 46509018

PROPERTIES

Hydrophobicity(logP) 4.6
Solubility Very slightly soluble

DETAILS

Description (English)
Item Information
Drug Groups approved
Description A phenothiazine antipsychotic used principally in the treatment of nausea; vomiting; and vertigo. It is more likely than chlorpromazine to cause extrapyramidal disorders. (From Martindale, The Extra Pharmacopoeia, 30th ed, p612)
Indication For the symptomatic management of psychotic disorders, short term management of nonpsychotic anxiety in patients with generalized anxiety disorder, and for the control of severe nausea and vomiting of various causes.
Pharmacology Prochlorperazine is a piperazine phenothiazine related to high-potency neuroleptics such as perphenazine. It shares many of the actions and adverse effects of the antipsychotics.
Toxicity Symptoms of central nervous system depression to the point of somnolence or coma. Agitation and restlessness may also occur. Other possible manifestations include convulsions, EKG changes and cardiac arrhythmias, fever and autonomic reactions such as hypotension, dry mouth and ileus; LD50=400mg/kg (orally in mice)
Affected Organisms
Humans and other mammals
Biotransformation Hepatic. Undergoes metabolism in the gastric mucosa and on first pass through the liver, CYP2D6 and/or CYP3A4.
Absorption Rapidly absorbed following oral administration
Half Life 6 to 8 hours
Protein Binding 91-99%
External Links
Wikipedia
RxList
Drugs.com

REFERENCES