5,6-Methylenedioxy-N-methyl-2-aminoindane
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File:MDMAI.svg | |
Systematic (IUPAC) name | |
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N-methyl-6,7-dihydro-5H-cyclopenta[f][1,3]benzodioxol-6-amine | |
Clinical data | |
Routes of administration | Oral |
Legal status | |
Legal status |
|
Identifiers | |
CAS Number | 132741-82-3 |
ATC code | none |
PubChem | CID 125559 |
ChemSpider | 111695 |
Chemical data | |
Formula | C11H13NO2 |
Molar mass | 191.226 g/mol[[Script error: No such module "String".]] |
Script error: No such module "collapsible list". | |
5,6-Methylenedioxy-N-methyl-2-aminoindane (MDMAI), is a drug developed in the 1990s by a team led by David E. Nichols at Purdue University. It acts as a non-neurotoxic and highly selective serotonin releasing agent (SSRA) in animals and a putative entactogen in humans.[1]
Chemistry
MDMAI can be thought of as a cyclised analogue of MDMA where the alpha-methyl carbon of the alkylamino side chain has been joined back round to the 6-position of the aromatic ring to form an indane ring system. This changes the core structure of the molecule from phenethylamine to aminoindane, and causes the pharmacological properties of the two compounds to be substantially different.[1]
See also
References
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Aminoindanes | |
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Aminotetralins | |
Phenethylamines (and amphetamines, cathinones, etc) | 2-Methyl-MDA • 4-CAB • 4-FA • 4-FMA • 4-MTA • 5-APDB • 5-Methyl-MDA • 6-APDB • 6-Methyl-MDA • Ariadne • BDB • BOH • Brephedrone • Butylone • DMMDA • DMMDA-2 • EBDB • EBDP • EDMA • Ethylone • Eutylone • Fenfluramine (also dexfenfluramine) • Flephedrone • IAP • IMP • Lophophine • MBDB • MBDP • MDA • MDDM • MDEA • MDIP • MDMA • MDMOH • MDMP • MDMPEA • MDOH • MDPEA • MDPH • MDPR • Mephedrone • Methedrone • Methylone • MMA • MMDA • MMDMA • NAP • Norfenfluramine • Pentylone • PMA • PMEA • PMMA • TAP |
Tryptamines |
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