
MDAI: Difference between revisions
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'''MDAI''' ('''5,6-Methylenedioxy-2-aminoindane''') 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 vitro and produces [[entactogen]] effects in humans similar to that of [[MDMA]]. | '''MDAI''' ('''5,6-Methylenedioxy-2-aminoindane''') 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 vitro and produces [[entactogen]] effects in humans similar to that of [[MDMA]]. | ||
Revision as of 21:38, 29 July 2014
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Chemical Nomenclature | |||||||||||||||||||||||||||||||
Common names | MDAI | ||||||||||||||||||||||||||||||
Substitutive name | 5,6-Methylenedioxy-2-aminoindane | ||||||||||||||||||||||||||||||
Systematic name | 6,7-Dihydro-5H-cyclopenta[f][1,3]benzodioxol-6-amine | ||||||||||||||||||||||||||||||
Class Membership | |||||||||||||||||||||||||||||||
Psychoactive class | Entactogen | ||||||||||||||||||||||||||||||
Chemical class | Aminoindane / MDxx | ||||||||||||||||||||||||||||||
Routes of Administration | |||||||||||||||||||||||||||||||
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Interactions | |||||||||||||||||||||||||||||||
MAOIs | |||||||||||||||||||||||||||||||
Serotonin releasers | |||||||||||||||||||||||||||||||
SSRIs | |||||||||||||||||||||||||||||||
5-HTP |
MDAI (5,6-Methylenedioxy-2-aminoindane) 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 vitro and produces entactogen effects in humans similar to that of MDMA.
Chemistry
The chemical structure of MDAI is indirectly derived from that of the illicit drug MDA, but the alpha-methyl group of the alkylamino amphetamine side chain has been bound back to the benzene nucleus to form an indane ring system, which changes its pharmacological properties substantially.[1]
Pharmacology
The chemical structure of MDAI is indirectly derived from that of the illicit drug MDA, but the alpha-methyl group of the alkyl]]amino amphetamine side chain has been bound back to the benzene nucleus to form an indane ring system, which changes its pharmacological properties substantially.[1]
Subjective effects
Toxicity and Harm Potential
Lethal dosage
Tolerance and addition potential
Legal Issues
See Also
References
- ↑ Monte AP, Marona-Lewicka D, Cozzi NV, Nichols DE. Synthesis and pharmacological examination of benzofuran, indan, and tetralin analogues of 3,4-(methylenedioxy)amphetamine. Journal of Medicinal Chemistry. 1993 Nov 12;36(23):3700-6. Template:DOI PMID 8246240