Home > Compound List > Product Information
Flupenthixol_Molecular_structure_CAS_2709-56-0)
Click picture or here to close

Flupenthixol

Catalog No. DB00875 Name DrugBank
CAS Number 2709-56-0 Website http://www.ualberta.ca/
M. F. C23H25F3N2OS Telephone (780) 492-3111
M. W. 434.5176096 Fax (780) 492-1071
Purity Email david.wishart@ualberta.ca
Storage Chembase ID: 753

SYNONYMS

IUPAC name
2-(4-{3-[2-(trifluoromethyl)-9H-thioxanthen-9-ylidene]propyl}piperazin-1-yl)ethan-1-ol
IUPAC Traditional name
flupenthixol
Brand Name
Fluanxol Depot
Fluanxol
Siplarol
Flupentixol
Depixol
Emergil
Flurentixol
Fluxanxol
Siplaril
Synonyms
Flupenthixole

DATABASE IDS

CAS Number 2709-56-0

PROPERTIES

Hydrophobicity(logP) 4.4
Solubility 0.000346 mg/ml

DETAILS

Description (English)
Item Information
Drug Groups approved
Description Flupentixol is an antipsychotic neuroleptic drug. It is a thioxanthene, and therefore closely related to the phenothiazines. Its primary use is as a long acting injection given two or three weekly to people with schizophrenia who have a poor compliance with medication and suffer frequent relapses of illness. It is a D1 and D2 receptor antagonist.
Indication For use in the treatment of schizophrenia and depression
Pharmacology Flupenthixol is an anxiolytic, antidepressive agent and a mood stabilizer. It inhibits the central monoamine receptors, particularly the dopamine D1 and D2 receptors. Therefore, it increases the amount of serotonin and noradrenaline that control mood and thinking, and improves mood.
Toxicity LD50=300 mk/kg (Oral in mice); LD50=791 mg/kg (Oral in rats); LD50=87 mk/kg (IV in mice); LD50=37 mg/kg (IV in rats)
Affected Organisms
Humans and other mammals
Biotransformation Mainly hepatic
Absorption Fairly slow and incomplete after oral administration
Half Life 19 to 39 hours
Protein Binding Highly bound to plasma proteins (>95%)
External Links
Wikipedia

REFERENCES