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Sultopride

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Sultopride
Sultopride.svg
Clinical data
Trade names Barnetil, Barnotil, Topral
AHFS/Drugs.com International Drug Names
Routes of
administration
Oral, IM
ATC code
Legal status
Legal status
  • In general: ℞ (Prescription only)
Pharmacokinetic data
Elimination half-life 3–5 hours
Identifiers
  • N-[(1-ethylpyrrolidin-2-yl)methyl]-5-ethylsulfonyl-2-methoxybenzamide
CAS Number
PubChem CID
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard (EPA)
ECHA InfoCard 100.053.293
Chemical and physical data
Formula C17H26N2O4S
Molar mass 354.47 g·mol−1
3D model (JSmol)
  • O=S(=O)(c1cc(c(OC)cc1)C(=O)NCC2N(CC)CCC2)CC
  • InChI=1S/C17H26N2O4S/c1-4-19-10-6-7-13(19)12-18-17(20)15-11-14(24(21,22)5-2)8-9-16(15)23-3/h8-9,11,13H,4-7,10,12H2,1-3H3,(H,18,20) checkY
  • Key:UNRHXEPDKXPRTM-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)

Sultopride (trade names Barnetil, Barnotil, Topral) is an atypical antipsychotic of the benzamide chemical class used in Europe, Japan, and Hong Kong for the treatment of schizophrenia. It was launched by Sanofi-Aventis in 1976. Sultopride acts as a selective D2 and D3 receptor antagonist. 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.

Pharmacology

Sultopride
Site Ki Species Ref
D2 1.6 Human
D3 3.8 Human



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