435293-66-6,MFCD09840695
Catalog No.:AA00DF8V

435293-66-6 | 4'-HYDROXY ATOMOXETINE

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1mg
≥98%
in stock  
$272.00   $190.00
- +
5mg
≥98%
in stock  
$1,072.00   $750.00
- +
10mg
≥98%
in stock  
$1,856.00   $1,299.00
- +
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA00DF8V
Chemical Name:
4'-HYDROXY ATOMOXETINE
CAS Number:
435293-66-6
Molecular Formula:
C17H21NO2
Molecular Weight:
271.3541
MDL Number:
MFCD09840695
SMILES:
CNCC[C@H](c1ccccc1)Oc1ccc(cc1C)O
Properties
Computed Properties
 
Complexity:
266  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
20  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0  
Rotatable Bond Count:
6  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
3.4  

Literature

Title: Development and validation of a liquid chromatography-tandem mass spectrometry assay for hair analysis of atomoxetine and its metabolites: Application in clinical practice.

Journal: Forensic science international 20120510

Title: Determination of atomoxetine metabolites in human plasma by liquid chromatography/tandem mass spectrometry and its application to a pharmacokinetic study.

Journal: Journal of chromatography. B, Analytical technologies in the biomedical and life sciences 20120215

Title: Synthesis and biological evaluation of the major metabolite of atomoxetine: elucidation of a partial kappa-opioid agonist effect.

Journal: Bioorganic & medicinal chemistry letters 20040802

Title: Effect of potent CYP2D6 inhibition by paroxetine on atomoxetine pharmacokinetics.

Journal: Journal of clinical pharmacology 20021101

Title: Identification of the human cytochromes P450 responsible for atomoxetine metabolism.

Journal: Drug metabolism and disposition: the biological fate of chemicals 20020301

Title: JT Brown, Single Dose Pharmacokinetics of Atomoxetine in Children.

Title: Bymaster FP, Katner JS, Nelson DL et al. Atomoxetine increases extracellular levels of norepinephrine and dopamine in prefrontal cortex of rat: a potential mechanism for efficacy in attention deficit/hyperactivity disorder. Neuropsychopharmacology. 2002 Nov;27(5):699-711.

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SDS
Tags:435293-66-6 Molecular Formula|435293-66-6 MDL|435293-66-6 SMILES|435293-66-6 4'-HYDROXY ATOMOXETINE
Catalog No.: AA00DF8V
435293-66-6,MFCD09840695
435293-66-6 | 4'-HYDROXY ATOMOXETINE
Pack Size: 1mg
Purity: ≥98%
in stock
$272.00 $190.00
Pack Size: 5mg
Purity: ≥98%
in stock
$1,072.00 $750.00
Pack Size: 10mg
Purity: ≥98%
in stock
$1,856.00 $1,299.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA00DF8V
Chemical Name: 4'-HYDROXY ATOMOXETINE
CAS Number: 435293-66-6
Molecular Formula: C17H21NO2
Molecular Weight: 271.3541
MDL Number: MFCD09840695
SMILES: CNCC[C@H](c1ccccc1)Oc1ccc(cc1C)O
Properties
Complexity: 266  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 1  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 20  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 2  
Isotope Atom Count: 0  
Rotatable Bond Count: 6  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 3.4  
Literature fold

Title: Development and validation of a liquid chromatography-tandem mass spectrometry assay for hair analysis of atomoxetine and its metabolites: Application in clinical practice.

Journal: Forensic science international20120510

Title: Determination of atomoxetine metabolites in human plasma by liquid chromatography/tandem mass spectrometry and its application to a pharmacokinetic study.

Journal: Journal of chromatography. B, Analytical technologies in the biomedical and life sciences20120215

Title: Synthesis and biological evaluation of the major metabolite of atomoxetine: elucidation of a partial kappa-opioid agonist effect.

Journal: Bioorganic & medicinal chemistry letters20040802

Title: Effect of potent CYP2D6 inhibition by paroxetine on atomoxetine pharmacokinetics.

Journal: Journal of clinical pharmacology20021101

Title: Identification of the human cytochromes P450 responsible for atomoxetine metabolism.

Journal: Drug metabolism and disposition: the biological fate of chemicals20020301

Title: JT Brown, Single Dose Pharmacokinetics of Atomoxetine in Children.

Title: Bymaster FP, Katner JS, Nelson DL et al. Atomoxetine increases extracellular levels of norepinephrine and dopamine in prefrontal cortex of rat: a potential mechanism for efficacy in attention deficit/hyperactivity disorder. Neuropsychopharmacology. 2002 Nov;27(5):699-711.

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