Мы используем файлы cookie.
Продолжая использовать сайт, вы даете свое согласие на работу с этими файлами.
Продолжая использовать сайт, вы даете свое согласие на работу с этими файлами.
Sultopride
Sultopride
Подписчиков: 0, рейтинг: 0
Clinical data | |
---|---|
Trade names | Barnetil, Barnotil, Topral |
AHFS/Drugs.com | International Drug Names |
Routes of administration |
Oral, IM |
ATC code | |
Legal status | |
Legal status |
|
Pharmacokinetic data | |
Elimination half-life | 3–5 hours |
Identifiers | |
| |
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) | |
| |
| |
NY (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
Site | Ki | Species | Ref |
---|---|---|---|
D2 | 1.6 | Human | |
D3 | 3.8 | Human |
Receptor (ligands) |
|
||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|
Transporter (blockers) |
|
||||||||||
Enzyme (inhibitors) |
|
||||||||||