ChemSpider 2D Image | Norketamine hydrochloride | C12H15Cl2NO

Norketamine hydrochloride

  • Molecular FormulaC12H15Cl2NO
  • Average mass260.160 Da
  • Monoisotopic mass259.053070 Da
  • ChemSpider ID21475083

More details:

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

2-Amino-2-(2-chlorophenyl)cyclohexanone hydrochloride (1:1) [ACD/IUPAC Name]
2-Amino-2-(2-chlorophényl)cyclohexanone, chlorhydrate (1:1) [French] [ACD/IUPAC Name]
2-Amino-2-(2-chlorphenyl)cyclohexanonhydrochlorid (1:1) [German] [ACD/IUPAC Name]
79499-59-5 [RN]
Cyclohexanone, 2-amino-2-(2-chlorophenyl)-, hydrochloride (1:1) [ACD/Index Name]
Norketamine hydrochloride
NORKETAMINE HYDROCHLORIDE, (R)-
NORKETAMINE HYDROCHLORIDE, (S)-
(±)-Norketamine hydrochloridemissing
[79499-59-5] [RN]
More...

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

QA4F2IDL56 [DBID]
UNII:QA4F2IDL56 [DBID]
0Y16VH028R [DBID]
409CNJ2726 [DBID]
MCI-186 | [DBID]
UN2811 [DBID]
  • Experimental Physico-chemical Properties
  • Miscellaneous

    • Safety:

      Sold for research purposes under agreement from Pfizer Inc. Tocris Bioscience 1970

    • Bio Activity:

      Glutamate (Ionotropic) Receptors Tocris Bioscience 1970
      Ion Channels Tocris Bioscience 1970
      Ketamine and Metabolites Tocris Bioscience 1970
      Ligand-gated Ion Channels Tocris Bioscience 1970
      Major metabolite of ketamine that is a potent non-competitive NMDA receptor antagonist (Ki = 3.6 ?M for displacement of [3H]-MK 801 in rat brain). Antinociceptive and anesthetic in vivo. Tocris Bioscience 1970
      Major metabolite of ketamine that is a potent non-competitive NMDA receptor antagonist (Ki = 3.6 ?M for displacement of [3H]-MK 801 in rat brain). Antinociceptive and anesthetic in vivo. R-enantiomer and S-enantiomer also available. Tocris Bioscience 1970
      Major metabolite of ketamine that is a potent non-competitive NMDA receptor antagonist (Ki = 3.6 muM for displacement of [3H]-MK 801 in rat brain). Antinociceptive and anesthetic in vivo. R-enantiomer and S-enantiomer also available. Tocris Bioscience 1970
      Potent, non-competitive NMDA antagonist Tocris Bioscience 1970
      Potent, non-competitive NMDA antagonist; antinociceptive Tocris Bioscience 1970
      Reagents Tocris Bioscience 1970

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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