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Definition and meaning of Propylamphetamine

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Propylamphetamine

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Propylamphetamine
Systematic (IUPAC) name
N-(1-methyl-2-phenylethyl)propan-1-amine
Identifiers
CAS number51799-32-7
ATC codenone
PubChem103544
Chemical data
FormulaC12H19N 
Mol. mass177.286 g/mol
SynonymsN-propyl-1-phenyl-propan-2-amine;
N-propylamphetamine
Pharmacokinetic data
Bioavailability ?
MetabolismHepatic
Half life ?
ExcretionRenal
Therapeutic considerations
Pregnancy cat. ?
Legal status
Routes ?


Propylamphetamine is a psychoactive drug and research chemical of the phenethylamine and amphetamine chemical classes which acts as a stimulant. It was first developed in the 1970s, mainly for research into the metabolism of,[1] and as a comparison tool to other amphetamines.[2]. Rodent studies have demonstrated propylamphetamine to be only slightly less potent and active than amphetamine.[3]

See also

References

  1. Nazarali AJ, Baker GB, Coutts RT, Pasutto FM. Amphetamine in rat brain after intraperitoneal injection of N-alkylated analogues. Progress in Neuropsychopharmacology and Biological Psychiatry. 1983;7(4-6):813-6.
  2. Valtier S, Cody JT. Evaluation of internal standards for the analysis of amphetamine and methamphetamine. Journal of Analytical Toxicology. 1995 Oct;19(6):375-80.
  3. Woolverton WL, Shybut G, Johanson CE. Structure-activity relationships among some d-N-alkylated amphetamines. Pharmacology Biochemistry and Behavior. 1980 Dec;13(6):869-76.

Propylamphetamine

From Wikipedia, the free encyclopedia

Jump to: navigation, search
Propylamphetamine
Systematic (IUPAC) name
N-(1-methyl-2-phenylethyl)propan-1-amine
Identifiers
CAS number51799-32-7
ATC codenone
PubChem103544
Chemical data
FormulaC12H19N 
Mol. mass177.286 g/mol
SynonymsN-propyl-1-phenyl-propan-2-amine;
N-propylamphetamine
Pharmacokinetic data
Bioavailability ?
MetabolismHepatic
Half life ?
ExcretionRenal
Therapeutic considerations
Pregnancy cat. ?
Legal status
Routes ?


Propylamphetamine is a psychoactive drug and research chemical of the phenethylamine and amphetamine chemical classes which acts as a stimulant. It was first developed in the 1970s, mainly for research into the metabolism of,[1] and as a comparison tool to other amphetamines.[2]. Rodent studies have demonstrated propylamphetamine to be only slightly less potent and active than amphetamine.[3]

See also

References

  1. ^ Nazarali AJ, Baker GB, Coutts RT, Pasutto FM. Amphetamine in rat brain after intraperitoneal injection of N-alkylated analogues. Progress in Neuropsychopharmacology and Biological Psychiatry. 1983;7(4-6):813-6.
  2. ^ Valtier S, Cody JT. Evaluation of internal standards for the analysis of amphetamine and methamphetamine. Journal of Analytical Toxicology. 1995 Oct;19(6):375-80.
  3. ^ Woolverton WL, Shybut G, Johanson CE. Structure-activity relationships among some d-N-alkylated amphetamines. Pharmacology Biochemistry and Behavior. 1980 Dec;13(6):869-76.

 

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