ChemSpider 2D Image | CP 99,994 (hydrochloride) | C19H26Cl2N2O

CP 99,994 (hydrochloride)

  • Molecular FormulaC19H26Cl2N2O
  • Average mass369.328 Da
  • Monoisotopic mass368.142212 Da
  • ChemSpider ID26232136

  • defined stereocentres - 2 of 2 defined stereocentres

More details:

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

(2S,3S)-N-(2-Methoxybenzyl)-2-phenyl-3-piperidinamindihydrochlorid [German] [ACD/IUPAC Name]
(2S,3S)-N-(2-Methoxybenzyl)-2-phenyl-3-piperidinamine dihydrochloride [ACD/IUPAC Name]
(2S,3S)-N-(2-Méthoxybenzyl)-2-phényl-3-pipéridinamine, dichlorhydrate [French] [ACD/IUPAC Name]
145148-39-6 [RN]
3-Piperidinamine, N-[(2-methoxyphenyl)methyl]-2-phenyl-, (2S,3S)-, hydrochloride (1:2) [ACD/Index Name]
CP 99,994 (hydrochloride)
(2S,3S)-N-[(2-Methoxyphenyl)methyl]-2-phenyl-3-piperidinamine dihydrochloride
[145148-39-6] [RN]
136982-36-0 [RN]
145148-39-6(DiHydrochloride); 136982-36-0 (Free Base).
More...
  • Experimental Physico-chemical Properties
  • Miscellaneous

    • Safety:

      Sold for research purposes under agreement from Pfizer Inc. Tocris Bioscience 3417

    • Bio Activity:

      7-TM Receptors Tocris Bioscience 3417
      High affinity NK1 antagonist Tocris Bioscience 3417
      High affinity NK1 antagonist (Ki = 0.145 nM in vitro). Also displays high ex vivo binding potency in gerbil striatum (IC50 = 36.8 nM). Attenuates endothelium-dependent contraction induced by substance P. Tocris Bioscience 3417
      High affinity NK1 antagonist (Ki = 0.145 nM in vitro). Also displays high ex vivo binding potency in gerbil striatum (IC50 = 36.8 nM). Attenuates endothelium-dependent contraction induced by substance P. Tocris Bioscience 3417
      Peptide Receptors Tocris Bioscience 3417
      Tachykinin Receptors Tocris Bioscience 3417

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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