SKF 83959 hydrobromide

  ( 6 citations )    
Product Datasheet
Catalog Number:2074
Chemical Name:6-Chloro-2,3,4,5-tetrahydro-3-methyl-1-(3-methylphenyl)-1H-3-benzazepine-7,8-diol
Product Details
Citations (6)
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Reviews
Biological Activity
Dopamine D1-like receptor partial agonist (Ki values are 1.18, 7.56, 920 and 399 nM for rat D1, D5, D2 and D3 receptors respectively). May act as an antagonist in vivo, producing anti-Parkinsonian effects and antagonizing the behavioral effects of cocaine. Shown to potentiate agonist binding of the σ1 receptor.
Technical Data
  • M.Wt:
    398.73
  • Formula:
    C18H20ClNO2.HBr
  • Solubility:
    Soluble to 50 mM in DMSO
  • Purity:
    >98
  • Storage:
    Store at RT
  • CAS No:
    67287-95-0
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis. All Tocris products are intended for laboratory research use only.
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Citations:

The citations listed below are publications that use Tocris products. Selected citations for SKF 83959 hydrobromide include:

6 Citations: Showing 1 - 6
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  1. Regulation of c-fos expression by the dopamine D1-D2 receptor heteromer.
    Authors: Perreault Et al.
    Neuroscience  2015;285:194
  2. A dopamine receptor contributes to paraquat-induced neurotoxicity in Drosophila.
    Authors: Cassar Et al.
    Pharmacol Biochem Behav  2015;24:197
  3. The dopamine D1-D2 receptor heteromer exerts a tonic inhibitory effect on the expression of amphetamine-induced locomotor sensitization.
    Authors: Shen Et al.
    Br J Pharmacol  2015;128:33
  4. Dopamine D1 and corticotrophin-releasing hormone type-2α receptors assemble into functionally interacting complexes in living cells.
    Authors: Fuenzalida Et al.
    PLoS One  2014;171:5650
  5. A physiological role for the dopamine D5 receptor as a regulator of BDNF and Akt signalling in rodent prefrontal cortex.
    Authors: Perreault Et al.
    Int J Neuropsychopharmacol  2013;16:477
  6. SKF83959, an agonist of phosphatidylinositol-linked D(1)-like receptors, promotes ERK1/2 activation and cell migration in cultured rat astrocytes.
    Authors: Huang Et al.
    Nat Chem Biol  2012;7:e49954

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