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Remoxipride

产品号 DB00409 公司名称 DrugBank
CAS号 80125-14-0 公司网站 http://www.ualberta.ca/
分子式 C16H23BrN2O3 电 话 (780) 492-3111
分子量 371.26942 传 真
纯 度 电子邮件 david.wishart@ualberta.ca
保 存 Chembase数据库ID: 292

产品价格信息

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产品别名

标题
Remoxipride
IUPAC标准名
3-bromo-N-{[(2S)-1-ethylpyrrolidin-2-yl]methyl}-2,6-dimethoxybenzamide
IUPAC传统名
remoxipride
别名
Remoxipride [Usan:Ban:Inn]
Remoxipridum [INN-Latin]
Romoxipride
Remoxiprida [INN-Spanish]

产品登记号

PubChem SID 46508689
PubChem CID 54477
CAS号 80125-14-0

产品性质

疏水性(logP) 2.9
溶解度 74 mg/L

产品详细信息

详细说明 (English)
Item Information
Drug Groups approved; withdrawn
Description An antipsychotic agent that is specific for dopamine D2 receptors. It has been shown to be effective in the treatment of schizophrenia. [PubChem]
Indication Remoxipride is an atypical antipsychotic once used for the treatment of schizophrenia.
Pharmacology Remoxipride, a substituted benzamide, is a selective D2 receptor antagonist. It has been shown to be effective in the treatment of schizophrenia. Some antipsychotics block domapinergic receptors as well as cholinergic, noradrenergic and histaminergic receptors. Remoxipride was developed to act specifically on the dopamine D2 receptor. As a consequence, several undesired side effects can occur. Patients often feel they are not taking any antipsychotic drug. It has a potent affinity for the sigma receptor, but it is unclear whether it is a sigma agonist or antagonist. The contribution of this property to its clinical profile is unknown. Blocking the D2 dopamine receptor is known to cause relapse in patients that have achieved remission from depression, and such blocking also counteracts the effectiveness of SSRI medication.
Affected Organisms
Humans and other mammals
Biotransformation No active metabolites
Absorption Rapidly absorbed. Absolute bioavailability is 90%.
Half Life 4-7 hours
Protein Binding 89-98%
External Links
Wikipedia

参考文献