Methylenedioxyphenethylamine

Methylenedioxyphenethylamine

Methylenedioxyphenethylamine
Systematic (IUPAC) name
2-(1,3-benzodioxol-5-yl)ethanamine
Clinical data
Pregnancy cat.
  • ?
Legal status
Routes Various
Pharmacokinetic data
Bioavailability ?
Metabolism ?
Half-life ?
Excretion ?
Identifiers
CAS number  YesY
ATC code ?
PubChem
DrugBank
ChemSpider
Synonyms 1,3-benzodioxolyl-5-ethanamine;
3,4-methylenedioxy-2-phenylethylamine
Chemical data
Formula C9H11NO2 
Mol. mass 165.18914 g/mol
 YesY   

3,4-Methylenedioxyphenethylamine (MDPEA), also known as homopiperonylamine, is a substituted phenethylamine formed by adding a methylenedioxy group to phenethylamine. It is structurally similar to MDA, but without the methyl group at the alpha position.

According to Alexander Shulgin in his book PiHKAL, MDPEA appears to be biologically inactive. This is likely because of extensive first-pass metabolism by the enzyme monoamine oxidase. However, if MDPEA were either used in high enough of doses (e.g., 1-2 grams), or in combination with a monoamine oxidase inhibitor (MAOI), it is probable that it would become sufficiently active, though it would likely have a relatively short duration of action. This idea is similar in concept to the use of selective MAOA inhibitors and selective MAOB inhibitors in augmentation of dimethyltryptamine (DMT) and phenethylamine (PEA), respectively.

See also

References

  1. ^ = WDU20111050614 "Ustawa z dnia 15 kwietnia 2011 r. o zmianie ustawy o przeciwdziałaniu narkomanii ( Dz.U. 2011 nr 105 poz. 614 )". Internetowy System Aktów Prawnych. Retrieved 17 June 2011. 

External links

  • PiHKAL: #115 MDPEA; 3,4-Methylenedioxyphenethylamine; Homopiperonylamine