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MMDA-2

From Wikipedia, the free encyclopedia
Psychedelic drug
Pharmaceutical compound
MMDA-2
Clinical data
Other names2-Methoxy-4,5-methylenedioxyamphetamine; 6-Methoxy-3,4-methylenedioxyamphetamine; 6-Methoxy-MDA; 6-MeO-MDA
Routes of
administration
Oral
ATC code
  • None
Legal status
Legal status
Identifiers
  • 1-(6-methoxy-1,3-benzodioxol-5-yl)propan-2-amine
CAS Number
PubChemCID
ChemSpider
UNII
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC11H15NO3
Molar mass209.245 g·mol−1
3D model (JSmol)
  • O1c2cc(c(OC)cc2OC1)CC(N)C

MMDA-2, also known as2-methoxy-4,5-methylenedioxyamphetamine or as6-methoxy-MDA, is apsychedelic drug of thephenethylamine,amphetamine, andMDxx families.[1] It is closely related toMMDA andMDA.[1]

Alexander Shulgin was likely the first tosynthesize MMDA-2.[1] In his bookPiHKAL (Phenethylamines I Have Known and Loved), the dose is listed as 25 to 50 mg, and theduration is listed as 8 to 12 hours.[1] Shulgin reports that MMDA-2 produces effects such as enhancedawareness,empathy, andvisual facilitation anddistortion, as well as someside effects likegastrointestinal upset andappetite loss.[1] He states that 30 mg is very similar to 80 mg of MDA, and also remarks that it would be impossible for anyone to have a bad experience on the drug at that dose.[1]

It has been found that MMDA-2, unlike MMDA but similarly to6-methyl-MDA, is very weak or negligible at inducing the release ofserotonin ordopamine,[2] and accordingly, does not produceamphetamine-like responses in animals indrug discrimination studies.[3] Instead, MMDA-2 is likely to act as a pureserotonin5-HT2 receptoragonist similarly to theDOx series of compounds, with activation of the serotonin5-HT2A receptor conferring its psychedelic effects.[4]

MMDA-2 has been sold as adesigner drug inJapan.[5]

See also

[edit]

References

[edit]
  1. ^abcdefShulgin A, Shulgin A (13 May 2016)."MMDA-2 (2-Methoxy-4,5-methylenedioxyamphetamine)".Pihkal: A Chemical Love Story. Transform Press.ISBN 978-0-9630096-0-9.
  2. ^McKenna DJ, Guan XM, Shulgin AT (March 1991)."3,4-Methylenedioxyamphetamine (MDA) analogues exhibit differential effects on synaptosomal release of 3H-dopamine and 3H-5-hydroxytryptamine".Pharmacology, Biochemistry, and Behavior.38 (3):505–512.doi:10.1016/0091-3057(91)90005-M.PMID 1829838.S2CID 2740262.
  3. ^Glennon RA, Yousif M, Naiman N, Kalix P (March 1987). "Methcathinone: a new and potent amphetamine-like agent".Pharmacology, Biochemistry, and Behavior.26 (3):547–551.doi:10.1016/0091-3057(87)90164-X.PMID 3575369.S2CID 5890314.
  4. ^Clare BW (2002). "QSAR of benzene derivatives: comparison of classical descriptors, quantum theoretic parameters and flip regression, exemplified by phenylalkylamine hallucinogens".Journal of Computer-Aided Molecular Design.16 (8–9):611–633.Bibcode:2002JCAMD..16..611C.doi:10.1023/A:1021966231380.PMID 12602954.S2CID 9948738.
  5. ^Min JZ, Shimizu Y, Toyo'oka T, Inagaki S, Kikura-Hanajiri R, Goda Y (October 2008). "Simultaneous determination of 11 designated hallucinogenic phenethylamines by ultra-fast liquid chromatography with fluorescence detection".Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences.873 (2):187–194.doi:10.1016/j.jchromb.2008.08.020.PMID 18789774.

External links

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