Product overview

Name (S)-(-)-Sulpiride
Purity >99%
Description Selective D2-like receptor antagonist. Active enantiomer.
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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

Solubility overview Soluble in DMSO (100 mM)
Storage instructions Room temperature
Storage of solutions Prepare and use solutions on the same day if possible. Store solutions at -20°C for up to one month if storage is required. Equilibrate to RT and ensure the solution is precipitate free before use.
Shipping Conditions Stable for ambient temperature shipping. Follow storage instructions on receipt.
Important This product is for RESEARCH USE ONLY and is not intended for therapeutic or diagnostic use. Not for human or veterinary use.

Calculators

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Chemical Data

Purity >99%
Chemical name (S)-(-)-5-Aminosulfonyl-N-[(1-ethyl-2-pyrrolidinyl)methyl]-2-methoxybenzamide
Molecular Weight 341.42
Chemical structure (S)-(-)-Sulpiride  [23672-07-3] Chemical Structure
Molecular Formula C15H23N3O4S
CAS Number 23672-07-3
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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