Exploring α,N-DMT. To explore a different substance…

Names:
α,N-DMT
Alpha-N
Tryptamine, α,N-dimethyl
3-[2-(Methylamino)propyl]indole
Indole, 3-[2-(methylamino)propyl]
α,N-Dimethyltryptamine
IUPAC name:
1-(1H-Indol-3-yl)-N-methylpropan-2-amine
5008 · C12H16N2 · 188.269
InChI=1S/C12H16N2/c1-9(13-2)7-10-8-14-12-6-4-3-5-11(10)12/h3-6,8-9,13-14H,7H2,1-2H3
HUWIYJREHSBOEO-UHFFFAOYSA-N This stereoisomer Any stereoisomer

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Repke, DB; Ferguson, WJ; Bates, DK. Synthesis of secondary methylalkylamines. Tetrahedron Lett., 1979, 20 (43), 4183–4184. 149 kB. https://doi.org/10.1016/S0040-4039(01)86538-2

Zhang, S; Fan, Y; Shi, Z; Cheng, S. DFT-based QSAR and action mechanism of phenylalkylamine and tryptamine hallucinogens. Chin. J. Chem., 1 Apr 2011, 29 (4), 623–630. 166 kB. https://doi.org/10.1002/cjoc.201190132 #58

Shulgin, AT. Basic Pharmacology and Effects. In Hallucinogens. A Forensic Drug Handbook; Laing, R; Siegel, JA, Eds., Academic Press, London, 2003; pp 67–137. 6.3 MB.

DMT
2,α-DMT
α-ET
NET
1,α-DMT
α,α-DMT
4-Me-α-MT
7-Me-AMT
N-Methylhomotryptamine
5-Ethyltryptamine
2787
Fenproporex
5786
CMMA
5-Me-AMT
21 July 2018 · Creative Commons BY-NC-SA ·