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MDAT
Chemical compound
Chemical compound
| Field | Value | |||
|---|---|---|---|---|
| image | 6,7-Methylenedioxy-2-aminotetralin.svg | |||
| image_class | skin-invert-image | |||
| width | 250px | |||
| class | Serotonin releasing agent; Entactogen | |||
| ATC_prefix | None | |||
| legal_status | Uncontrolled | |||
| index2_label | hydrochloride | |||
| CAS_number_Ref | ||||
| CAS_number | 101625-35-8 | |||
| CAS_number2_Ref | ||||
| CAS_number2 | 3446-21-8 | |||
| UNII_Ref | ||||
| UNII | 28IR5LC41Q | |||
| UNII2_Ref | ||||
| UNII2 | BOX4U52EET | |||
| PubChem | 36483 | |||
| ChemSpiderID | 33531 | |||
| synonyms | 6,7-MDAT; 6,7-Methylenedioxy-2-aminotetralin | |||
| IUPAC_name | 5,6,7,8-tetrahydrobenzo[f][1,3]benzodioxol-6-amine | |||
| C | 11 | H=13 | N=1 | O=2 |
| SMILES | C3Cc1cc2OCOc2cc1CC3N |
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. 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. Hence, MDAT is considered likely to be a non-neurotoxic, putative entactogen in humans.
References
References
- (February 1990). "Nonneurotoxic tetralin and indan analogues of 3,4-(methylenedioxy)amphetamine (MDA)". Journal of Medicinal Chemistry.
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