5-Methyl-MDA

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5-Methyl-MDA
File:5-Methyl-MDA.svg
Systematic (IUPAC) name
1-(7-methyl-1,3-benzodioxol-5-yl)propan-2-amine
Clinical data
Routes of
administration
Oral
Legal status
Legal status
Identifiers
CAS Number 749191-14-8
204916-89-2 (HCl)
ATC code none
PubChem CID 10012829
ChemSpider 8188403
Chemical data
Formula C11H15NO2
Molar mass 193.242 g/mol[[Script error: No such module "String".]]
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3-Methyl-4,5-methylenedioxyamphetamine (5-Methyl-MDA) is an entactogen and psychedelic drug of the amphetamine class. It is a ring-methylated derivative of MDA and a structural isomer of MDMA.[1] Drug discrimination studies showed that 5-methyl-MDA substitutes for MDA, MMAI, DOI, and LSD, but not amphetamine, suggesting that it produces a mix of entactogen and hallucinogenic effects without any stimulant effects.[2]

5-Methyl-MDA acts as a selective serotonin releasing agent (SSRA) with IC50 values of 107 nM, 11,600 nM, and 1,494 nM for serotonin, dopamine, and norepinephrine efflux.[1] It is over 5x more potent than MDA, with a suitable active dose possibly being around 15-25 mg.[1][2] 2-Methyl-MDA is also much more potent than MDA, but is not quite as potent as 5-methyl-MDA.[1] Both 6-methyl-MDA and 6-methyl-MDMA (also known as Madam-6) are inactive, likely due to steric hindrance.[1][3]

Recent research has used data on 2-methyl-MDA and 5-methyl-MDA to help guide computer modeling of the serotonin transporter complex.[4]

The synthesis of 5-methyl-MDA can be found online.[2]

See also

References

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  3. PIHKAL #98
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