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Remoxipride

Catalog No. DB00409 Name DrugBank
CAS Number 80125-14-0 Website http://www.ualberta.ca/
M. F. C16H23BrN2O3 Telephone (780) 492-3111
M. W. 371.26942 Fax (780) 492-1071
Purity Email david.wishart@ualberta.ca
Storage Chembase ID: 292

SYNONYMS

IUPAC name
3-bromo-N-{[(2S)-1-ethylpyrrolidin-2-yl]methyl}-2,6-dimethoxybenzamide
IUPAC Traditional name
remoxipride
Synonyms
Remoxipride [Usan:Ban:Inn]
Remoxipridum [INN-Latin]
Romoxipride
Remoxiprida [INN-Spanish]

DATABASE IDS

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

PROPERTIES

Hydrophobicity(logP) 2.9
Solubility 74 mg/L

DETAILS

Description (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Drug Groups approved; withdrawn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

REFERENCES