Skip to content
sultopride

Structure via PubChem · Public domain (PubChem)

EntityQ4445779· pop 13· linked from 505 articles

sultopride

Sign in to save

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.

Chemical data

Formula
C17H26N2O4S
Molecular weight
354.5 g/mol
IUPAC name
N-[(1-ethylpyrrolidin-2-yl)methyl]-5-ethylsulfonyl-2-methoxybenzamide
SMILES
CCN1CCCC1CNC(=O)C2=C(C=CC(=C2)S(=O)(=O)CC)OC
InChIKey
UNRHXEPDKXPRTM-UHFFFAOYSA-N
XLogP
1.6
Polar surface area
84.1 Ų
H-bond donors
1
H-bond acceptors
5
Formal charge
0

via PubChem

Drug data · ChEMBL

Max clinical phase
Phase 2
Molecule type
Small molecule
Indications
psychosis

via ChEMBL · EBI

Research

1,689 papers

via PubMed

Wikidata facts

Has part
carbon
Mass
354.161
Show 5 more facts
chemical formula
C₁₇H₂₆N₂O₄S
canonical SMILES
CCN1CCCC1CNC(=O)C2=C(C=CC(=C2)S(=O)(=O)CC)OC
Commons category
Sultopride
subject has role
dopamine antagonist
MCN code
2933.99.43
Sources (3)

via Wikidata · CC0

~1 min read

Encyclopedic overview

2 sections
Contents
  • Pharmacology
  • References

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 == {| class="wikitable sortable" |+Sultopride !Site !Ki !Species !Ref |- |D2 |1.6 |Human | |- |D3 |3.8 |Human | |}

Excerpted from Wikipedia’s “sultopride” article, available under the CC BY-SA 4.0 licence.