Phenylisobutylamine , also known as α-ethylphenethylamine , Butanphenamine , B or AEPEA ,[1] is a stimulant drug of the phenethylamine class. It is a higher homologue of amphetamine , differing from amphetamine's molecular structure only by the substitution of the methyl group at the alpha position of the side chain with an ethyl group . Compared to amphetamine, phenylisobutylamine has strongly reduced dopaminergic effects, and instead acts as a selective norepinephrine releasing agent .[citation needed ] The dextroisomer of phenylisobutylamine partially substitutes for dextroamphetamine in rats.[1]
A number of derivatives of phenylisobutylamine are known, including BDB , MBDB , EBDB , butylone (bk-MBDB), eutylone (bk-EBDB), Ariadne (α-Et-DOM), 4-CAB , and 4-MAB .
"Phenylisobutylamine" is in fact a chemical misnomer because isobutylamine itself contains a branched chain. The correct name after this style for this class of compound would be "phenylsec butylamine".
See also [ edit ]
References [ edit ]
Adamantanes
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Alkylamines
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1-(4-Methylphenyl)-2-aminobutane
1-Phenyl-2-(piperidin-1-yl)pentan-3-one
1-Methylamino-1-(3,4-methylenedioxyphenyl)propane
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β