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Biological Data Biological description Selective D2 -like receptor antagonist. Active enantiomer. (Ki values are 2.5 and 8 nM at D2 , D3 , >1000 nM at D4 , D5 and D1 receptors respectively). Antipsychotic. Active in vivo .
Solubility & Handling Storage instructions Room temperature
Solubility overview Soluble in DMSO (100 mM)
Important This product is for RESEARCH USE ONLY and is not intended for therapeutic or diagnostic use. Not for human or veterinary use.
Chemical Data Chemical name (S )-(-)-5-Aminosulfonyl-N -[(1-ethyl-2-pyrrolidinyl)methyl]-2-methoxybenzamide
Chemical structure
Molecular Formula C15 H23 N3 O4 S
PubChem identifier 688272
SMILES NS(C1=CC(C(NC[C@]2([H])CCCN2CC)=O)=C(OC)C=C1)(=O)=O
InChiKey BGRJTUBHPOOWDU-NSHDSACASA-N
References for (S)-(-)-Sulpiride References are publications that support the biological activity of the product
Clozapine and sulpiride but not haloperidol or olanzapine activate brain DNA demethylation. Dong E et al (2008) Proc Natl Acad Sci U S A 105(36) : 13614-9. Antipsychotic drugs: importance of dopamine receptors for mechanisms of therapeutic actions and side effects. Strange PG (2001) Pharmacol Rev 53(1) : 119-33. Cloning of the gene for a human dopamine D5 receptor with higher affinity for dopamine than D1. Sunahara RK et al (1991) Nature 350(6319) : 614-9.
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Selective D2 -like receptor antagonist. Active enantiomer.