
CAS 1217686-14-0
:Formula:C17H21NO2
InChI:InChI=1S/C17H21NO2/c1-13-12-15(19)8-9-16(13)20-17(10-11-18-2)14-6-4-3-5-7-14/h3-9,12,17-19H,10-11H2,1-2H3/t17-/m1/s1/i2D3
InChI key:PPXQPRLGNSJNJM-NVNSKBCASA-N
SMILES:[2H]C([2H])([2H])NCC[C@H](C1=CC=CC=C1)OC2=C(C=C(C=C2)O)C
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4-Hydroxyatomoxetine-d3
CAS:4-Hydroxyatomoxetine-d3Formula:C17H18D3NO2Purity:98.89%Molecular weight:274.374'-Hydroxy Atomoxetine-d3 Hemioxalate
CAS:Formula:C17H18D3NO2·5C2H2O4Color and Shape:White To Off-White SolidMolecular weight:274.38 0.5*90.034-Hydroxyatomoxetine-D3
CAS:4-Hydroxyatomoxetine D3, a deuterium variant, is Atomoxetine's active metabolite, metabolized by CYP2D6, an adrenergic reuptake blocker.Formula:C17H21NO2Purity:98%Color and Shape:SolidMolecular weight:274.37264’-Hydroxy Atomoxetine-d3
CAS:Controlled ProductApplications A labelled metabolite of Atomoxetine.
References Creighton, C.J., et al.: Bioorg. Med. Chem. Lett., 14, 15, 4083 (2004)Formula:C17H18D3NO2Color and Shape:NeatMolecular weight:274.374’-Hydroxy atomoxetine-d3
CAS:4’-Hydroxyatomoxetine-d3 is a research tool for studying protein interactions and receptor-ligand binding. It is an inhibitor of ion channels and has been shown to inhibit the activity of ligand-gated ion channels. 4’-Hydroxyatomoxetine-d3 has also been shown to act as an inhibitor on the norepinephrine transporter (NET) and serotonin transporter (SERT), which are involved in the reuptake of these neurotransmitters. 4’-Hydroxyatomoxetine-d3 exhibits high purity, with CAS number 1217686-14-0, and can be used in life science research or cell biology experiments.
Formula:C17H21NO2Purity:Min. 95%Molecular weight:274.37 g/mol






