Found 1 result

Search term: FHYWNBUFNGHNCP-UHFFFAOYSA-N (Found by InChIKey (full match))
ChemSpider 2D Image | MFCD03792727 | C18H21BrClNO2

MFCD03792727

  • 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]
67287-95-0 [RN]
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]
6-chloro-7,8-dihydroxy-3-methyl-1-(3-methylphenyl)-2,3,4,5-tetrahydro-1H-3-benzazepine hydrobromide
80751-85-5 [RN]
MFCD03792727
N-methyl-6-chloro-1-(3-methylphenyl)-2,3,4,5-tetrahydro-3-benzazepine-7,8-diol hydrobromide
SKF 83959 (hydrobromide)
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Validated by Experts, Validated by Users, Non-Validated, Removed by Users

7NB1Z2NM8O [DBID]
CHEBI:63996 [DBID]
UNII:7NB1Z2NM8O [DBID]
EU-0101067 [DBID]
S2816_SIGMA [DBID]
  • Experimental Physico-chemical Properties
  • Miscellaneous

    • Chemical Class:

      A hydrobromide salt prepared from <element>N</element>-methyl-6-chloro-1-(3-methylphenyl)-2,3,4,5-tetrahydro-3-benzazepine-7,8-diol and one equivalent of hydrogen bromide. Dopamine D1-like receptor pa rtial 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 antagonising the be havioral effects of cocaine. ChEBI CHEBI:63996
      A hydrobromide salt prepared from N-methyl-6-chloro-1-(3-methylphenyl)-2,3,4,5-tetrahydro-3-benzazepine-7,8-diol and one equivalent of hydrogen bromide. Dopamine D1-like receptor pa; rtial 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 antagonising the behavioral effects of cocaine. ChEBI https://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI:63996
      A hydrobromide salt prepared from N-methyl-6-chloro-1-(3-methylphenyl)-2,3,4,5-tetrahydro-3-benzazepine-7,8-diol and one equivalent of hydrogen bromide. Dopamine D1-like receptor partial agonist (Ki v alues 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 antagonising the behavioral effects of cocaine. ChEBI CHEBI:63996

    • 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 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 sigma1 receptor. Tocris Bioscience 2074
      Dopamine Receptors Tocris Bioscience 2074

Predicted data is generated using the ACD/Labs Percepta Platform - PhysChem Module, version: 14.00

No predicted properties have been calculated for this compound.

Click to predict properties on the Chemicalize site


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