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Names

IPTA
4-Isopropylthioamphetamine

IUPAC names

1-{4-[(Propan-2-yl)sulfanyl]phenyl}propan-2-amine
1-[4-(Propan-2-ylsulfanyl)phenyl]propan-2-amine

ID 6333 · Formula C₁₂H₁₉NS · Molecular weight 209.351

InChI InChI=1S/C12H19NS/c1-9(2)14-12-6-4-11(5-7-12)8-10(3)13/h4-7,9-10H,8,13H2,1-3H3

InChI Key OJIOFXBQHYHQSL-UHFFFAOYSA-N This stereoisomer Any stereoisomer

SMILES CC(Cc1ccc(cc1)SC(C)C)N

ChemSpider 8234488
PubChem 10058934

Shulgin Index See #103 MTA · Table 3Page 324Row 33

Phenethylamine: Von der Strucktur zur Funktion IPTA: 6.3 (36) 404

Scorza, MC; Carrau, C; Silveira, R; Zapata-Torres, G; Cassels, BK; Reyes-Parada, M. Monoamine oxidase inhibitory properties of some methoxylated and alkylthio amphetamine derivatives Biochem. Pharmacol., 15 Dec 1997, 54 (12), 1361–1369. 697 kB. https://doi.org/10.1016/S0006-2952(97)00405-X #6 ITA

Reyes-Parada, M; Iturriaga-Vasquez, P; Cassels, BK. Amphetamine derivatives as monoamine oxidase inhibitors Front. Pharmacol., 23 Jan 2020, 10 1590. 1.9 MB. https://doi.org/10.3389/fphar.2019.01590 #ITA

Vallejos, G; Rezende, MC; Cassels, BK. Charge-transfer interactions in the inhibition of MAO-A by phenylisopropylamines – a QSAR study J. Comput. Aided Mol. Des., 1 Feb 2002, 16 (2), 95–103. 105 kB. https://doi.org/10.1023/A:1016344030772 #3

4-MTDMA · N,N-Dimethyl-4-methylthioamphetamine · MTDMA · PAL-1063

4-MTEA · N-Ethyl-4-methylthioamphetamine · MTEA

4-EtS-MA · 4-Ethylthiomethamphetamine

1394

4-MTMB · α-Ethyl-4-methylthiophenethylamine

4-Propylthioamphetamine

TCE

7 Dec 2019 · · Isomer Design