ChemSpider 2D Image | N-methyl-6-chloro-1-(3-methylphenyl)-2,3,4,5-tetrahydro-3-benzazepine-7,8-diol hydrobromide | C18H21BrClNO2

N-methyl-6-chloro-1-(3-methylphenyl)-2,3,4,5-tetrahydro-3-benzazepine-7,8-diol hydrobromide

  • Molecular FormulaC18H21BrClNO2
  • Average mass398.722 Da
  • Monoisotopic mass397.044403 Da
  • ChemSpider ID10131933

More details:






Validated by Experts, Validated by Users, Non-Validated, Removed by Users

1H-3-Benzazepine-7,8-diol, 6-chloro-2,3,4,5-tetrahydro-3-methyl-1-(3-methylphenyl)-, hydrobromide (1:1) [ACD/Index Name]
6-Chlor-3-methyl-1-(3-methylphenyl)-2,3,4,5-tetrahydro-1H-3-benzazepin-7,8-diolhydrobromid (1:1) [German] [ACD/IUPAC Name]
6-Chloro-3-methyl-1-(3-methylphenyl)-2,3,4,5-tetrahydro-1H-3-benzazepine-7,8-diol hydrobromide (1:1) [ACD/IUPAC Name]
6-Chloro-3-méthyl-1-(3-méthylphényl)-2,3,4,5-tétrahydro-1H-3-benzazépine-7,8-diol, bromhydrate (1:1) [French] [ACD/IUPAC Name]
N-methyl-6-chloro-1-(3-methylphenyl)-2,3,4,5-tetrahydro-3-benzazepine-7,8-diol hydrobromide
[67287-95-0]
67287-95-0 [RN]
6-Chloro-2,3,4,5-tetrahydro-3-methyl-1-(3-methylphenyl)-1H-3-benzazepine-7,8-diol
6-chloro-3-methyl-1-(3-methylphenyl)-2,3,4,5-tetrahydro-1H-3-benzazepine-7,8-diol hydrobromide
6-Chloro-7,8-dihydroxy-3-methyl-1-(3-methylphenyl)-2,3,4,5-tetrahydro-1H-3-benzazepine
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Validated by Experts, Validated by Users, Non-Validated, Removed by Users

CHEBI:63996 [DBID]
EU-0101067 [DBID]
S2816_SIGMA [DBID]
  • Experimental Physico-chemical Properties
  • Miscellaneous
    • Bio Activity:

      7-TM Receptors Tocris Bioscience 2074
      D1 and D5 Receptors Tocris Bioscience 2074
      D1-like partial agonist Tocris Bioscience 2074
      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 eff ects and antagonizing the behavioral effects of cocaine. Shown to potentiate agonist binding of the ?1 receptor. Tocris Bioscience 2074
      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 ?1 receptor. Tocris Bioscience 2074
      Dopamine Receptors Tocris Bioscience 2074

Predicted data is generated using the ACD/Labs Percepta Platform - PhysChem Module

No predicted properties have been calculated for this compound.

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