| Weight | 390.933 g/mol |
|---|---|
| Formula | C17H27ClN2O4S |
| Hydrogen Acceptors | 5 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 7 |
sultopride hydrochloride (23694-17-9, 55619-22-2)
Solian · amisulpride · sultopride
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- Neurochemical Characteristics of Amisulpride, an Atypical Dopamine D2/D3 Receptor Antagonist with Both Presynaptic and Limbic Selectivity (Journal of Pharmacology and Experimental Therapeutics, 1997)
- Amisulpride, an unusual "atypical" antipsychotic: a meta-analysis of randomized controlled trials. (American Journal of Psychiatry, 2002)
- Psychopharmacological Profile of Amisulpride: An Antipsychotic Drug with Presynaptic D2/D3 Dopamine Receptor Antagonist Activity and Limbic Selectivity (Journal of Pharmacology and Experimental Therapeutics, 1997)
- Treatment of negative symptoms in schizophrenia with amisulpride. (British Journal of Psychiatry, 1995)
- Amisulpride is a potent 5-HT7 antagonist: relevance for antidepressant actions in vivo (Psychopharmacology, 2009)
- Celecoxib treatment in an early stage of schizophrenia: Results of a randomized, double-blind, placebo-controlled trial of celecoxib augmentation of amisulpride treatment (Schizophrenia Research, 2010)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Solian
- amisulpride
- sultopride
- DAN 2163
- N-(ethyl-1-pyrrolidinyl- 2-methyl)methoxy-2-ethylsulfonyl-5-benzamide
- LIN 1418
- Barnetil
-
SMILESCCN1CCCC1CNC(=O)C2=C(C=CC(=C2)S(=O)(=O)CC)OC.Cl
-
InChIKeyIGOWMQPOGQYFFM-UHFFFAOYSA-N
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Synthesis
5-Ethylsulfonyl-2-methoxybenzoyl chloride
+
2-(Aminomethyl)-1-ethylpyrrolidine
(Schotten-Baumann amide from acid)
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sultopride hydrochloride
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