Sultopride

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Sultopride
File:Sultopride structure.svg
Systematic (IUPAC) name
N-[(1-ethylpyrrolidin-2-yl)methyl]-5-ethylsulfonyl-2-methoxy-benzamide
Clinical data
Routes of
administration
Oral, IM
Legal status
Legal status
  • ℞ (Prescription only)
Pharmacokinetic data
Biological half-life 3-5 hours
Identifiers
CAS Number 53583-79-2
ATC code N05AL02 (WHO)
PubChem CID 5357
ChemSpider 5164
Chemical data
Formula C17H26N2O4S
Molar mass 354.46 g/mol[[Script error: No such module "String".]]
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Sultopride (Barnetil, Barnotil, Topral) is a typical antipsychotic of the benzamide chemical class used in Europe, Japan, and Hong Kong for the treatment of schizophrenia.[1][2][3] It was launched by Sanofi-Aventis in 1976.[1] Sultopride acts as a selective D2 and D3 receptor antagonist.[4] It has also been shown to have clinically-relevant affinity for the GHB receptor as well, a property it shares in common with amisulpride and sulpiride.[5]

See also

References

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ja:スルトプリド ru:Сультоприд
  1. 1.0 1.1 José Miguel Vela; Helmut Buschmann; Jörg Holenz; Antonio Párraga; Antoni Torrens (2007). Antidepressants, Antipsychotics, Anxiolytics: From Chemistry and Pharmacology to Clinical Application. Weinheim: Wiley-VCH. ISBN 3-527-31058-4. 
  2. Swiss Pharmaceutical Society (2000). Index Nominum 2000: International Drug Directory (Book with CD-ROM). Boca Raton: Medpharm Scientific Publishers. ISBN 3-88763-075-0. 
  3. European Drug Index, 4th Edition. Boca Raton: CRC Press. 1998. ISBN 3-7692-2114-1. 
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