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6-Methyl-MDA

From Wikipedia, the free encyclopedia
(Redirected from4,5-Methylenedioxy-2-methylamphetamine)
Psychoactive drug
Pharmaceutical compound
6-Methyl-MDA
Clinical data
Routes of
administration
Oral[1]
ATC code
  • None
Legal status
Legal status
Identifiers
  • 1-(6-Methyl-1,3-benzodioxol-5-yl)propan-2-amine
CAS Number
PubChemCID
ChemSpider
UNII
ChEMBL
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC11H15NO2
Molar mass193.246 g·mol−1
3D model (JSmol)
  • O1c2cc(c(cc2OC1)CC(N)C)C
  • InChI=1S/C11H15NO2/c1-7-3-10-11(14-6-13-10)5-9(7)4-8(2)12/h3,5,8H,4,6,12H2,1-2H3 checkY
  • Key:HCFHWXDIZOAUTQ-UHFFFAOYSA-N checkY
  (verify)

6-Methyl-MDA, also known as6-methyl-3,4-methylenedioxyamphetamine is anentactogen andpsychedelicdrug of theamphetamine andMDxx families.[2] It was firstsynthesized in the late 1990s by a team includingDavid E. Nichols atPurdue University while investigatingderivatives of3,4-methylenedioxyamphetamine (MDA) and3,4-methylenedioxy-N-methylamphetamine (MDMA).[2]

6-Methyl-MDA hasIC50 values of 783 nM, 28,300 nM, and 4,602 nM forinhibiting thereuptake ofserotonin,dopamine, andnorepinephrine in ratsynaptosomes.[2] In animal studies it substitutes forMBDB,MMAI,LSD, and2,5-dimethoxy-4-iodoamphetamine (DOI), though notamphetamine, but only partially and at high doses.[2] Thus, while several-fold lesspotent than itsanalogues2-methyl-MDA and5-methyl-MDA, and approximately half as potent as MDA, 6-methyl-MDA is still significantlyactive.[2]

According toDaniel Trachsel and colleagues, 6-methyl-MDA is active at a dose of 160 mgorally and has aduration of 8 hours.[1]

See also

[edit]

References

[edit]
  1. ^abTrachsel D, Lehmann D, Enzensperger C (2013).Phenethylamine: von der Struktur zur Funktion [Phenethylamines: From Structure to Function]. Nachtschatten-Science (in German) (1 ed.). Solothurn: Nachtschatten-Verlag. pp. 656–657, 746, 830.ISBN 978-3-03788-700-4.OCLC 858805226. Archived fromthe original on 21 August 2025.
  2. ^abcdeParker MA, Marona-Lewicka D, Kurrasch D, Shulgin AT, Nichols DE (March 1998). "Synthesis and pharmacological evaluation of ring-methylated derivatives of 3,4-(methylenedioxy)amphetamine (MDA)".Journal of Medicinal Chemistry.41 (6):1001–5.CiteSeerX 10.1.1.688.9559.doi:10.1021/jm9705925.PMID 9526575.

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