MDAT

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6,7-Methylenedioxy-2-aminotetralin (MDAT) is a drug 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.

References

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v t e Entactogens
Phenylalkylamines	Phenethylamines: Lophophine MDMPEA MDPEA Metaescaline Amphetamines: 2-Methyl-MDA 4-FA 4-FMA 4-MTA 5-APDI 5-MAPDI 5-Methyl-MDA 6-APT 6-Methyl-MDA DiFMDA DMMDA DMMDA-2 EDA EDMA MDA MDDM MDEA MDIP MDMA MDMOH MDOH MDPR MMA MMDA MMDA-2 MMDMA PMA PMEA PMMA Benzofurans: 5-APB 5-MAPB 5-APDB 5-MAPDB 5-EAPB 6-APB 6-MAPB 6-APDB 6-MAPDB 6-EAPB Cathinones: Brephedrone Butylone Ethylone Eutylone Flephedrone Mephedrone Methedrone Methylone Pentylone Others: 4-CAB Ariadne BDB EBDB EBDP MDMP MDPH MBDB MBDP
Cyclized phenyl- alkylamines	Aminoindanes: 5-IAI AMMI ETAI MDAI MDMAI MMAI NM-2-AI TAI Aminotetralins: 6-CAT MDAT MDMAT
Tryptamines	4-Methyl-αET αET αMT
Others	Naphthylisopropylamine Methamnetamine