ChemSpider 2D Image | Atomoxetine hydrochloride | C17H22ClNO

Atomoxetine hydrochloride

  • Molecular FormulaC17H22ClNO
  • Average mass291.816 Da
  • Monoisotopic mass291.138977 Da
  • ChemSpider ID49515

  • defined stereocentres - 1 of 1 defined stereocentres

More details:

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

(-)-N-Methyl-3-phenyl-3-(o-tolyloxy)propylamine hydrochloride
(3R)-N-methyl-3-(2-methylphenoxy)-3-phenyl-1-propanamine hydrochloride
(3R)-N-Methyl-3-(2-methylphenoxy)-3-phenyl-1-propanamine hydrochloride (1:1) [ACD/IUPAC Name]
(3R)-N-Méthyl-3-(2-méthylphénoxy)-3-phényl-1-propanamine, chlorhydrate (1:1) [French] [ACD/IUPAC Name]
(3R)-N-Methyl-3-(2-methylphenoxy)-3-phenyl-1-propanaminhydrochlorid (1:1) [German] [ACD/IUPAC Name]
(3R)-N-méthyl-3-(2-méthylphénoxy)-3-phénylpropan-1-amine chlorhydrate [French]
(3R)-N-methyl-3-(2-methylphenoxy)-3-phenylpropan-1-amine hydrochloride
(3R)-N-Methyl-3-(2-methylphenoxy)-3-phenylpropan-1-amine hydrochloride (1:1)
(3R)-N-Methyl-3-(2-methylphenoxy)-3-phenylpropan-1-aminhydrochlorid [German]
(gR)-N-Methyl-g-(2-methylphenoxy)benzenepropanamine Hydrochloride
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Validated by Experts, Validated by Users, Non-Validated, Removed by Users

5318974 [DBID]
CCRIS 4693 [DBID]
D02574 [DBID]
LY 139603 [DBID]
LY-135252 [DBID]
LY-139603 [DBID]
  • Experimental Physico-chemical Properties
  • Predicted Physico-chemical Properties
  • Miscellaneous

    • Chemical Class:

      The hydrochloride salt of atomoxetine. ChEBI https://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI:331697, CHEBI:331697

    • Bio Activity:

      Adrenergic Transporters Tocris Bioscience 2011
      Atomoxetine Hcl(LY 139603; Tomoxetine Hcl) is a potent and selective noradrenalin re-uptake inhibitor (Ki values are 5, 77 and 1451 nM for inhibition of radioligand binding to human NET, SERT and DAT respectively). MedChem Express http://www.medchemexpress.com/benfotiamine.html
      Atomoxetine Hcl(LY 139603; Tomoxetine Hcl) is a potent and selective noradrenalin re-uptake inhibitor (Ki values are 5, 77 and 1451 nM for inhibition of radioligand binding to human NET, SERT and DAT respectively). MedChem Express HY-17385
      Neurotransmitter Transporters Tocris Bioscience 2011
      Others MedChem Express HY-17385
      Potent and selective noradrenalin re-uptake inhibitor (Ki values are 5, 77 and 1451 nM for inhibition of radioligand binding to human NET, SERT and DAT respectively). Displays minimal affinity for a r ange of other neurotransmitter receptors and transporters (Ki > 1 ?M). Antidepressant. Tocris Bioscience 2011
      Potent and selective noradrenalin re-uptake inhibitor (Ki values are 5, 77 and 1451 nM for inhibition of radioligand binding to human NET, SERT and DAT respectively). Displays minimal affinity for a range of other neurotransmitter receptors and transporters (Ki > 1 ?M). Antidepressant. Tocris Bioscience 2011
      Potent and selective noradrenalin re-uptake inhibitor (Ki values are 5, 77 and 1451 nM for inhibition of radioligand binding to human NET, SERT and DAT respectively). Displays minimal affinity for a range of other neurotransmitter receptors and transporters (Ki > 1 muM). Antidepressant. Tocris Bioscience 2011
      Potent and selective noradrenalin re-uptake inhibitor (Ki values are 5, 77 and 1451 nM for inhibition of radioligand binding to human NET, SERT and DAT respectively). Displays minimal affinity for a range of other neurotransmitter receptors and transporters (Ki > 1 muM). Antidepressant. Deuterated analog also available. Tocris Bioscience 2011
      Potent, selective noradrenalin re-uptake inhibitor Tocris Bioscience 2011
      Transporters Tocris Bioscience 2011

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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