Propylamphetamine
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| Systematic (IUPAC) name | |
|---|---|
| N-(1-methyl-2-phenylethyl)propan-1-amine | |
| Clinical data | |
| Pregnancy cat. | ? |
| Legal status | ? |
| Pharmacokinetic data | |
| Metabolism | Hepatic |
| Excretion | Renal |
| Identifiers | |
| CAS number | 51799-32-7 |
| ATC code | None |
| PubChem | CID 103544 |
| ChemSpider | 11655332 |
| Synonyms | N-propyl-1-phenyl-propan-2-amine; N-propylamphetamine |
| Chemical data | |
| Formula | C12H19N |
| Mol. mass | 177.286 g/mol |
| SMILES | eMolecules & PubChem |
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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] A study in rats found propylamphetamine to be 1/4 as potent and active as amphetamine.[3]
[edit] See also
[edit] References
- ^ Nazarali, A. J.; Baker, G. B.; Coutts, R. T.; Pasutto, F. M. (1983). "Amphetamine in rat brain after intraperitoneal injection of N-alkylated analogues". Progress in neuro-psychopharmacology & biological psychiatry 7 (4–6): 813–816. PMID 6686713.
- ^ Valtier, S.; Cody, J. T. (1995). "Evaluation of internal standards for the analysis of amphetamine and methamphetamine". Journal of analytical toxicology 19 (6): 375–380. PMID 8926730.
- ^ Woolverton, W. L.; Shybut, G.; Johanson, C. E. (1980). "Structure-activity relationships among some d-N-alkylated amphetamines". Pharmacology, biochemistry, and behavior 13 (6): 869–876. PMID 7208552.
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