Details
Stereochemistry | RACEMIC |
Molecular Formula | C11H15NO.ClH |
Molecular Weight | 213.704 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.CC(N(C)C)C(=O)C1=CC=CC=C1
InChI
InChIKey=APOWZIQNQJSLKG-UHFFFAOYSA-N
InChI=1S/C11H15NO.ClH/c1-9(12(2)3)11(13)10-7-5-4-6-8-10;/h4-9H,1-3H3;1H
Metamfepramone (dimethylcathinone, dimethylpropion, and dimepropion) was synthesized by various routes in the 1930s and 1940s and clinically evaluated as anorectic as well as a treatment of hypotension and symptoms
of the common cold. It was widely used for the treatment of the common cold or hypotonic conditions. Due to its stimulating properties and its rapid metabolism resulting in major degradation products such as methylpseudoephedrine and methcathinone, it has been considered relevant for doping controls by the World Anti-Doping Agency (WADA). Metamfepramone was marketed as an appetite suppressant, but was made illegal in 2006.
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Choline pivaloyl esters improve in rats cognitive and memory performances impaired by scopolamine treatment or lesions of the nucleus basalis of Meynert. | 2004 Feb 19 |
|
Doping control analysis of metamfepramone and two major metabolites using liquid chromatography-tandem mass spectrometry. | 2009 |
Patents
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/19661559
One capsule (accounting for a total of 10mg
of metamfepramone-HCl), was orally ingested
Route of Administration:
Oral
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100000085922
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233-289-9
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DTXSID00905920
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SUB03185MIG
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6Y816E97O1
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3084061
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10105-90-5
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ACTIVE MOIETY
SUBSTANCE RECORD