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Flupenthixol

产品号 DB00875 公司名称 DrugBank
CAS号 2709-56-0 公司网站 http://www.ualberta.ca/
分子式 C23H25F3N2OS 电 话 (780) 492-3111
分子量 434.5176096 传 真
纯 度 电子邮件 david.wishart@ualberta.ca
保 存 Chembase数据库ID: 753

产品价格信息

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产品别名

标题
Flupenthixol
IUPAC标准名
2-(4-{3-[2-(trifluoromethyl)-9H-thioxanthen-9-ylidene]propyl}piperazin-1-yl)ethan-1-ol
IUPAC传统名
flupenthixol
商标名
Fluanxol Depot
Fluanxol
Siplarol
Flupentixol
Depixol
Emergil
Flurentixol
Fluxanxol
Siplaril
别名
Flupenthixole

产品登记号

CAS号 2709-56-0

产品性质

疏水性(logP) 4.4
溶解度 0.000346 mg/ml

产品详细信息

详细说明 (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

参考文献