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Chemical structure of CAS 83015-26-3

Atomoxetine

In Stock•Starting at $231 for 5 mg•Purity ≥ 98%
CAS No.83015-26-3
MDL No.MFCD06804608
MFC17H21NO
MW255.35
InChI KeyVHGCDTVCOLNTBX-QGZVFWFLSA-N
CUSTOM SYNTHESISPRECLINICAL SUPPORT

Pricing & Availability

Pack SizePurityPriceAvailabilityAction
5 mg98%$231In Stock
10 mg98%$359In Stock
50 mg98%$1120In Stock
Custom synthesis and bulk supply options are available upon request.

Product Information

Atomoxetine is a secondary amino compound with methyl and 3-(2-methylphenoxy)-3-phenylpropan-1-yl groups. It functions as an adrenergic uptake inhibitor, antidepressant, xenobiotic, and environmental contaminant. It is an aromatic ether, a secondary amino compound, and a member of the toluene class.

CAS No.83015-26-3
Product NameAtomoxetine

Biological Targets

SLC6A2

Associated Conditions

social anxiety disorder·Oppositional defiant disorder·Tourette syndrome·autism·alcohol dependence·
* The information provided here is compiled from public sources and is for reference only.

Related Articles

Studies related to this compound and its mechanism of action

Identification of the human cytochromes P450 responsible for atomoxetine metabolism.

Drug metabolism and disposition: the biological fate of chemicals • Vol. 30, Issue 3 • 2002
PMID: 11854152DOI: 10.1124/dmd.30.3.319

The norepinephrine transporter gene and attention-deficit hyperactivity disorder.

American journal of medical genetics • Vol. 114, Issue 3 • 2002
PMID: 11920844DOI: 10.1002/ajmg.10193

Tomoxetine (Eli Lilly & Co).

Current opinion in investigational drugs (London, England : 2000) • Vol. 3, Issue 2 • 2002
PMID: 12020059

Comparison of the subjective, physiological, and psychomotor effects of atomoxetine and methylphenidate in light drug users.

Drug and alcohol dependence • Vol. 67, Issue 2 • 2002
PMID: 12095664DOI: 10.1016/s0376-8716(02)00053-4

Documentation

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