6-APT
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Chemical compoundTemplate:SHORTDESC:Chemical compound
Pharmaceutical compoundTemplate:SHORTDESC:Pharmaceutical compound
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| Routes of administration | Oral |
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| E number | {{#property:P628}} |
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| ECHA InfoCard | {{#property:P2566}}Lua error in Module:EditAtWikidata at line 29: attempt to index field 'wikibase' (a nil value). |
| Chemical and physical data | |
| Formula | C13H19N |
| Molar mass | 189.302 g·mol−1 |
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6-(2-Aminopropyl)tetralin (6-APT), also sometimes called tetralinylaminopropane (TAP), is a drug of the amphetamine class which acts as a selective serotonin releasing agent (SSRA).[1] It has IC50 values of 121 nM, 6,436 nM, and 3,371 nM for inhibiting the reuptake of serotonin, dopamine, and norepinephrine, respectively.[1] Though it possesses an appreciable in vitro profile, in animal drug discrimination studies it was not found to substitute for MMAI or amphetamine and to only partially substitute for MBDB.[1] This parallels Alexander Shulgin's finding that EDMA (the 1,4-benzodioxine analogue of 6-APT) is limitedly active,[2] and appears to indicate that the pharmacokinetics of both EDMA and 6-APT may not be favorable.[1]
See also
[edit | edit source]References
[edit | edit source]| DRAsTooltip Dopamine releasing agents |
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