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Names

5-Chloro-AMT
5-Chloro-α-methyltryptamine
PAL-542

IUPAC name

1-(5-Chloro-1H-indol-3-yl)propan-2-amine

ID 741 · Formula C₁₁H₁₃ClN₂ · Molecular weight 208.687

Tags Tryptamine

InChI InChI=1S/C11H13ClN2/c1-7(13)4-8-6-14-11-3-2-9(12)5-10(8)11/h2-3,5-7,14H,4,13H2,1H3

InChI Key QMKOQSCXSYPIPB-UHFFFAOYSA-N This stereoisomer Any stereoisomer

SMILES CC(Cc1c[nH]c2c1cc(Cl)cc2)N

ChemSpider 12303
PubChem 12833
Wikidata Q19877216
Wikipedia 5-Chloro-αMT
Wikipedia, see also List of substituted α-alkyltryptamines
Project Response 5Cl-α-MT (2232-21)
aipsin.com 5-Cl-AMT (Iss. 17, May 2021: III-91)
aipsin.com 5-Cl-AMT (Iss. 10, Oct 2020: I-132)

Dinger, J; Woods, C; Brandt, SD; Meyer, MR; Maurer, HH. Cytochrome P450 inhibition potential of new psychoactive substances of the tryptamine class Toxicol. Lett., 1 Jan 2016, 241, 82-94. 2.6 MB. https://doi.org/10.1016/j.toxlet.2015.11.013

Wagmann, L; Brandt, SD; Kavanagh, PV; Maurer, HH; Meyer, MR. In vitro monoamine oxidase inhibition potential of alpha-methyltryptamine analog new psychoactive substances for assessing possible toxic risks Toxicol. Lett., 17 Apr 2017, 272, 84–93. 1.9 MB. https://doi.org/10.1016/j.toxlet.2017.03.007

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 #5-Cl-AMT

4-Chloro-AMT · 4-Chloro-α-methyltryptamine

Epibatidine

7-Chloro-AMT · 7-Chloro-α-methyltryptamine

7 Dec 2019 · · Isomer Design