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MDAT

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
MDAT
Clinical data
Other names6,7-MDAT; 6,7-Methylenedioxy-2-aminotetralin
Drug classSerotonin releasing agent;Entactogen
ATC code
  • None
Legal status
Legal status
  • In general: uncontrolled
Identifiers
  • 5,6,7,8-tetrahydrobenzo[f][1,3]benzodioxol-6-amine
CAS Number
PubChemCID
ChemSpider
UNII
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC11H13NO2
Molar mass191.230 g·mol−1
3D model (JSmol)
  • C3Cc1cc2OCOc2cc1CC3N

MDAT, also known as6,7-methylenedioxy-2-aminotetralin, is adrug of the2-aminotetralin family developed in the 1990s by a team atPurdue University led byDavid E. Nichols.[1] It appears to act as aserotonin releasing agent based on rodentdrug discrimination assays comparing it toMDMA, in which it fully substitutes for, and additionally lacks any kind ofserotonergic neurotoxicity.[1] Hence, MDAT is considered likely to be a non-neurotoxic, putativeentactogen in humans.

See also

[edit]

References

[edit]
  1. ^abNichols DE, Brewster WK, Johnson MP, Oberlender R, Riggs RM (February 1990). "Nonneurotoxic tetralin and indan analogues of 3,4-(methylenedioxy)amphetamine (MDA)".Journal of Medicinal Chemistry.33 (2):703–10.doi:10.1021/jm00164a037.PMID 1967651.

External links

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