SCH 23390 hydrochloride
Tocris Bioscience | Catalog # 0925
Key Product Details
Description
Alternative Names
Product Description
SCH 23390 hydrochloride is a potent dopamine receptor antagonist (Ki values are 0.2 nM and 0.3 nM at D1 and D5 receptor sub-types, respectively). Also an agonist at 5-HT2C receptors in vitro (Ki values are 6.3 - 9.3 nM). Blocks quinpirole-induced Kir3 (GIRK) currents (EC50 = 268 nM) independently of receptors.
Product Specifications for SCH 23390 hydrochloride
Molecular Weight
Formula
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CAS Number
PubChem ID
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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 | |||
| water | 32.42 | 100 with gentle warming | |
| Ethanol | 16.21 | 50 |
Preparing Stock Solutions for SCH 23390 hydrochloride
The following data is based on the product molecular weight 324.24.
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 | 3.08 mL | 15.42 mL | 30.84 mL |
| 5 mM | 0.62 mL | 3.08 mL | 6.17 mL |
| 10 mM | 0.31 mL | 1.54 mL | 3.08 mL |
| 50 mM | 0.06 mL | 0.31 mL | 0.62 mL |
Calculators
Background References
References are publications that support the biological activity of the product. See our Citations tab to view 137 publications citing the usage of this product.
- Kuzhikandathil and Oxford Classic D1 DA receptor antagonist R-(+)-7-chloro-8-hydroxy-3-methyl-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepine hydrochloride (SCH23390) directly inhibits G protein-coupled inwardly rectifying potassium channels. Mol.Pharmacol. 2002 PMID: 12065762
- Briggs Activation of the 5-HT1C receptor expressed in Xenopus oocytes by the benzazepines SCH 23390 and SKF 38393. Br.J.Pharmacol. 1991 PMID: 1687364
- Millan The "selective" DA D1 receptor antagonist, SCH23390, is a potent and high efficacy agonist against cloned human serotonin2C receptors. Psychopharmacology 2001 PMID: 11465634
- Bourne SCH 23390: The first selective DA D1-like receptor antagonist. CNS Drug Rev. 2001 PMID: 11830757
Product Documents for SCH 23390 hydrochloride
Certificate of Analysis
To download a Certificate of Analysis, please enter a lot or batch number in the search box below.
Product Specific Notices for SCH 23390 hydrochloride
For research use only
Citations for SCH 23390 hydrochloride
Customer Reviews for SCH 23390 hydrochloride (3)
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Species: HumanCell Line/Tissue: Stem cell - derived neuronsVerified Customer | Posted 10/15/2020SCH‐23390 was in use as a dopamine receptor antagonist. Being applied at stem cell – derived cultured neurons (10 nM concentration) together with sulpiride, caused an increase of amplitudes of evoked post-synaptic potentials generated by NMDA receptors (see illustration). Preparation of 10 mM water stocks requires sonication.
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Species: RatAssay Type: In VivoVerified Customer | Posted 01/22/2019At a dose that did not alter responding during food self-administration (6 micrograms/kg), systemic injections of SCH 23390 blocked responding during cue-induced reinstatement of food seeking tests.
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Species: MouseAssay Type: In VivoVerified Customer | Posted 10/26/2018Our lab has used SCH23390 to block dopaminergic D1 receptors and to check its effect on locomotion. Mice were injected with this drug and we noticed that SCH23390 decreased the average speed during a 5-minute test.
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