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-benzodioxineanalogue 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
References
- 1 2 3 4 Monte AP, Marona-Lewicka D, Cozzi NV, Nichols DE (noviembre de 1993). "Síntesis y examen farmacológico de análogos de benzofurano, indano y tetralina de 3,4-(metilendioxi)anfetamina". Journal of Medicinal Chemistry . 36 (23): 3700– 3706. doi : 10.1021/jm00075a027 . PMID 8246240 .
- ↑ Shulgin A, Shulgin A (13 de mayo de 2016). "EDMA · 3,4-Etilendioxi-N-metilanfetamina" . Pihkal: Una historia de amor química . Transform Press. ISBN 978-0-9630096-0-9.
- Medicamentos sin código ATC asignado.
- Anfetaminas sustituidas
- Tetralinas
- Agentes liberadores de serotonina
- Entactógenos