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5-Methyl-MDA

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
5-Methyl-MDA
Clinical data
Routes of
administration
Oral
ATC code
  • None
Legal status
Legal status
Identifiers
  • 1-(7-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)
  • O2COc1c2cc(CC(N)C)cc1C
  • InChI=1S/C11H15NO2/c1-7-3-9(4-8(2)12)5-10-11(7)14-6-13-10/h3,5,8H,4,6,12H2,1-2H3 checkY
  • Key:OLENSVFSNAULML-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)

5-Methyl-MDA, also known as5-methyl-3,4-methylenedioxyamphetamine, is anentactogen andpsychedelicdesigner drug of theamphetamine class. It is aring-methylatedhomologue ofMDA and astructural isomer ofMDMA.[1]

Pharmacology

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5-Methyl-MDA acts as aselective serotonin releasing agent (SSRA) withIC50 values of 107nM, 11,600nM, and 1,494nM forserotonin,dopamine, andnorepinephrine release, respectively.[1]

2-methyl-MDA and 5-methyl-MDA have been used to help guide computer modelling of theserotonin transporter complex.[2]

Society and culture

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Legal status

[edit]

International

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5-Methyl-MDA is not scheduled by theUnited Nations'Convention on Psychotropic Substances.[3]

United States

[edit]

5-Methyl-MDA is not explicitlyscheduled at thefederal level in theUnited States,[4] however 5-Methyl-MDA is a structural isomer of MDMA, and so sales orpossession could potentially be prosecuted under theFederal Analogue Act.[5]

Canada

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As per theSafe Streets and Communities Act, 5-Methyl-MDA, along with all other amphetamines, is a Schedule I controlled substance under theControlled Drugs and Substances Act.

See also

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References

[edit]
  1. ^abParker 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.doi:10.1021/jm9705925.PMID 9526575.
  2. ^Walline CC, Nichols DE, Carroll FI, Barker EL (June 2008)."Comparative molecular field analysis using selectivity fields reveals residues in the third transmembrane helix of the serotonin transporter associated with substrate and antagonist recognition".The Journal of Pharmacology and Experimental Therapeutics.325 (3):791–800.doi:10.1124/jpet.108.136200.PMC 2637348.PMID 18354055.
  3. ^"Convention on Psychotropic Substances, 1971". Archived fromthe original on 2022-01-19. Retrieved2016-06-09.
  4. ^"§1308.11 Schedule I." Archived fromthe original on 2009-08-27. Retrieved2016-06-09.
  5. ^Erowid Analog Law Vault : Federal Controlled Substance Analogue Act Summary

External links

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