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Diethylpropion

Catalog No. DB00937 Name DrugBank
CAS Number 134-80-5 Website http://www.ualberta.ca/
M. F. C13H19NO Telephone (780) 492-3111
M. W. 205.29606 Fax (780) 492-1071
Purity Email david.wishart@ualberta.ca
Storage Chembase ID: 813

SYNONYMS

IUPAC name
2-(diethylamino)-1-phenylpropan-1-one
IUPAC Traditional name
diethylpropion
Brand Name
Amfepramone
Keramin
Prefamone
Anfamon
Cegramine
Danylen
Dobesin
Silutin
Tepanil Ten-tab
Amfepramon
Amphepramon
Amphepramone
Frekentine
Keramik
Magrene
Modulor
Neobes
Nopropiophenone
Parabolin
Regenon
Regenon hydrochloride
Tenuate
Tenuate Dospan
Tenuate hydrochloride
Tepanil
Adiposon
Anorex
Derfon
Moderatan
Obesitex
Reginon
Tylinal
Synonyms
Amfepramone Hydrochloride
alpha-Diethylaminopropiophenone
alpha-Benzoyltriethylamine
Anfepramona [INN-Spanish]
DEA No. 1610
Diethylpropione hydrochloride
Diethylpropione
Amfepramonum [INN-Latin]
Amfepramone HCL
Amphepramonum hydrochloride
Diethylcathinone
Diethylpropion HCL
Diethylpropion Hydrochloride
Amfepramone

DATABASE IDS

PubChem CID 7029
PubChem SID 46506622
CAS Number 134-80-5

PROPERTIES

Hydrophobicity(logP) 2.8

DETAILS

Description (English)
Item Information
Drug Groups illicit; approved
Description A appetite depressant considered to produce less central nervous system disturbance than most drugs in this therapeutic category. It is also considered to be among the safest for patients with hypertension. (From AMA Drug Evaluations Annual, 1994, p2290)
Indication Used in the management of exogenous obesity as a short-term adjunct (a few weeks) in a regimen of weight reduction based on caloric restriction.
Pharmacology Diethylpropion is a sympathomimetic stimulant drug marketed as an appetite suppressant. Chemically, it is the N,N-diethyl analog of cathinone. Its mechanism of action is similar to other appetite suppressants such as sibutramine, phentermine and dextroamphetamine.
Toxicity The reported oral LD50 for mice is 600 mg/kg, for rats is 250 mg/kg and for dogs is 225 mg/kg. Manifestation of acute overdosage include restlessness, tremor, hyperreflexia, rapid respiration, confusion, assaultiveness, hallucinations, and panic states.
Affected Organisms
Humans and other mammals
Biotransformation Extensively metabolized through a complex pathway of biotransformation involving N-dealkylation and reduction. Many of these metabolites are biologically active and may participate in the therapeutic action of diethylpropion.
Absorption Diethylpropion is rapidly absorbed from the GI tract after oral administration.
Half Life Using a phosphorescence assay that is specific for basic compounds containing benzoyl group, the plasma half-life of the aminoketone metabolites is estimated to be between 4 to 6 hours.
Elimination Diethylpropion is rapidly absorbed from the GI tract after oral administration and is extensively metabolized through a complex pathway of biotransformation involving N-dealkylation and reduction. Diethylpropion and/or its active metabolites are believed to cross the blood-brain barrier and the placenta. Diethylpropion and its metabolites are excreted mainly by the kidney.
References
Adan RA, Vanderschuren LJ, la Fleur SE: Anti-obesity drugs and neural circuits of feeding. Trends Pharmacol Sci. 2008 Apr;29(4):208-17. Epub 2008 Mar 18. [Pubmed]
Arias HR, Santamaria A, Ali SF: Pharmacological and neurotoxicological actions mediated by bupropion and diethylpropion. Int Rev Neurobiol. 2009;88:223-55. [Pubmed]
External Links
Wikipedia
RxList
PDRhealth
Drugs.com

REFERENCES

  • Adan RA, Vanderschuren LJ, la Fleur SE: Anti-obesity drugs and neural circuits of feeding. Trends Pharmacol Sci. 2008 Apr;29(4):208-17. Epub 2008 Mar 18. Pubmed
  • Arias HR, Santamaria A, Ali SF: Pharmacological and neurotoxicological actions mediated by bupropion and diethylpropion. Int Rev Neurobiol. 2009;88:223-55. Pubmed