Remoxipride hydrochloride

Discontinued Product

0916 has been discontinued.
View all Non-selective Dopamine Receptor Antagonists products.
Remoxipride hydrochloride | CAS No. 73220-03-8 | Non-selective Dopamine Receptor Antagonists
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Description: Selective D2-like antagonist

Chemical Name: (S)-(-)-3-Bromo-N-[(1-ethyl-2-pyrrolidinylmethyl]2,6-dimethoxybenzamide hydrochloride

Product Details
Citations (1)
Reviews

Biological Activity

Remoxipride hydrochloride is a dopamine D2 receptor antagonist showing selectivity over D3 and D4 receptors (Ki values are ~ 300, ~ 1600, and ~ 2800 nM for D2, D3 and D4 receptors respectively). Exhibits antipsychotic activity in vivo with no extrapyramidal side effects. 50-fold more potent than sulpiride in antagonising the effects of apomorphine in the rat.

Technical Data

M.Wt:
407.73
Formula:
C16H23BrN2O3.HCl
Solubility:
Soluble to 100 mM in water
Storage:
Store at RT
CAS No:
73220-03-8

The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
Tocris products are intended for laboratory research use only, unless stated otherwise.

Background References

  1. High-throughput genotoxicity assay identifies antioxidants as inducers of DNA damage response and cell death.
    Fox JT, Sakamuru S, Huang R
    Proc. Natl. Acad. Sci. U.S.A., 2012;109(14):5423-8.
  2. In vivo effects of remoxipride and aromatic ring metabolites in the rat.
    Ahlenius et al.
    J.Pharmacol.Exp.Ther., 1997;283:1356
  3. Binding characteristics of remoxipride and its metabolites to DA D2 and D3 receptors.
    Mohell et al.
    Eur.J.Pharmacol., 1993;238:121
  4. Development of a new antipsychotic remoxipride.
    Sedvall
    Acta Psychiatr.Scand.Suppl., 1990;358:1
  5. DA receptor pharmacology.
    Seeman and Van Tol
    Trends Pharmacol.Sci., 1994;15:264

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Citation for Remoxipride hydrochloride

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