(S)-Remoxipride hydrochloride hydrate
(S)-Remoxipride ((-)-Remoxipride) hydrochloride hydrate ((S)-Remoxipride hydrochloride hydrate) is a selective dopamine D2-receptor antagonist with an IC50 value of 1.57 μM. (S)-Remoxipride hydrochloride hydrate can be used for the research of psychotic disorder.
For research use only. We do not sell to patients.
- CAS No.: 117591-79-4
- Formula: C16H26BrClN2O4
- Molecular Weight:425.75
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
To place orders, for customer services and technical support, please contact: MedChemExpress USA
Tel: 609-228-6898 E-mail: [email protected] [email protected]
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Biological Activity
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Chemical Information
- Protocols
- Purity & Documentation
- References
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Help & FAQs
All Dopamine Receptor Isoforms
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Biological Activity
Description
IC50 & Target
[1]|
D2 Receptor 1.57 μM (IC50) |
D1 Receptor >100 μM (IC50) |
Chemical Information
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CAS No. 117591-79-4
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Molecular Weight 425.75
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Formula C16H26BrClN2O4
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SMILES
O=C(NC[C@H]1N(CC)CCC1)C2=C(OC)C=CC(Br)=C2OC.Cl.O
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Synonyms
(-)-Remoxipride hydrochloride hydrate
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Please store the product under the recommended conditions in the Certificate of Analysis.
Protocols
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Cell Cytotoxicity Assay
Cytotoxicity assays are usually based on the assessment of cell membrane damage, which can also be indirectly detected by measuring cell viability. Detection methods include MTT assay, CKK-8 assay, LDH assay and ATP assay, etc.
Purity & Documentation
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
(S)-Remoxipride hydrochloride hydrate Related Classifications
HY-101313B Related Classifications
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