(S)-(-)-Sulpiride
Tocris Bioscience | Catalog # 0895
Key Product Details
Description
Product Description
(S)-(-)-Sulpiride is an active enantiomer. Selective D2-like dopamine antagonist (Ki values are ~ 0.015, ~ 0.013, 1, ~ 45 and ~ 77 μM at D2, D3, D4, D1 and D5 receptors respectively).
Racemate also available.
Product Specifications for (S)-(-)-Sulpiride
Molecular Weight
Formula
Storage
Purity
Chemical Name
CAS Number
PubChem ID
InChI Key
SMILES
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
Solubility
| Solvent | Max Conc. mg/mL | Max Conc. mM | |
|---|---|---|---|
| Solubility | |||
| DMSO | 34.14 | 100 | |
| Ethanol | 3.41 | 10 with gentle warming |
Preparing Stock Solutions for (S)-(-)-Sulpiride
The following data is based on the product molecular weight 341.42.
Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which all affect the solvent volumes required to prepare stock solutions.
| Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
|---|---|---|---|
| 1 mM | 2.93 mL | 14.64 mL | 29.29 mL |
| 5 mM | 0.59 mL | 2.93 mL | 5.86 mL |
| 10 mM | 0.29 mL | 1.46 mL | 2.93 mL |
| 50 mM | 0.06 mL | 0.29 mL | 0.59 mL |
Calculators
Background References
References are publications that support the biological activity of the product. See our Citations tab to view 80 publications citing the usage of this product.
- Seeman and Van Tol DA receptor pharmacology. TiPS 1994 PMID: 7940991
- Seeman and Van Tol DA D4 receptors bind inactive (+)-aporphines, suggesting neuroleptic role. Sulpiride not stereoselective. Eur.J.Pharmacol. 1993 PMID: 8097160
Product Documents for (S)-(-)-Sulpiride
Product Specific Notices for (S)-(-)-Sulpiride
For research use only
Citations for (S)-(-)-Sulpiride
Customer Reviews for (S)-(-)-Sulpiride (1)
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Species: HumanCell Line/Tissue: Stem cell - derived neuronsVerified Customer | Posted 10/15/2020(S)‐sulpiride (Sul) was in use to block D2 dopamine receptors and thus prevent D2-mediated suppression of NMDA receptors response. The compound worked as expected, generating a discernible increase of amplitudes of NMDA-receptor – mediated evoked post-synaptic potentials in cultured dopamine neurons when applied with SCH‐23390 (see illustration). No problem with dissolution in DMSO for 10 mM stock.
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