MDAT

Chemical compound From Wikipedia, the free encyclopedia

MDAT, also known as 6,7-methylenedioxy-2-aminotetralin, is a drug of the 2-aminotetralin family developed in the 1990s by a team at Purdue University led by David E. Nichols.[1] It appears to act as a serotonin releasing agent based on rodent drug discrimination assays comparing it to MDMA, in which it fully substitutes for, and additionally lacks any kind of serotonergic neurotoxicity.[1] Hence, MDAT is considered likely to be a non-neurotoxic, putative entactogen in humans.

Other names6,7-MDAT; 6,7-Methylenedioxy-2-aminotetralin
ATC code
  • None
Legal status
  • In general: uncontrolled
Quick facts Clinical data, Other names ...
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
PubChem CID
ChemSpider
UNII
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC11H13NO2
Molar mass191.230 g·mol−1
3D model (JSmol)
  • C3Cc1cc2OCOc2cc1CC3N
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References

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