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Exploring N-Methylhomotryptamine. To explore a different substance…

Name

N-Methylhomotryptamine

IUPAC name

3-(1H-Indol-3-yl)-N-methylpropan-1-amine

ID 5740 · Formula C₁₂H₁₆N₂ · Molecular weight 188.269

InChI InChI=1S/C12H16N2/c1-13-8-4-5-10-9-14-12-7-3-2-6-11(10)12/h2-3,6-7,9,13-14H,4-5,8H2,1H3

InChI Key NSHWYAHUTQARKB-UHFFFAOYSA-N This stereoisomer Any stereoisomer

SMILES CNCCCc1c[nH]c2c1cccc2

ChemSpider 14015624
PubChem 21472501

Sinhababu, AK; Ghosh, AK; Borchardt, RT. Molecular mechanism of action of 5,6-dihydroxytryptamine. Synthesis and biological evaluation of 4-methyl-, 7-methyl- and 4,7-dimethyl-5,6-dihydroxytryptamines. J. Med. Chem., 1 Sep 1985, 28 (9), 1273–1279. 1.0 MB. https://doi.org/10.1021/jm00147a027

Kalir, A; Szara, S. Synthesis and pharmacological activity of alkylated tryptamines. J. Med. Chem., 1 May 1966, 9 (3), 341–344. 482 kB. https://doi.org/10.1021/jm00321a017

DMT

2,α-DMT · 2-Me-AMT · 2-Me-α-MT · Alpha-2

Alpha-N · α,N-DMT

AET · Etryptamine · α-ET

NET

1,α-DMT

α,α-DMT

4,α-DMT · 4-Me-AMT · 4-Me-α-MT · MP-809

7-Me-AMT · α,7-DMT

5-Ethyltryptamine

2787

Fenproporex

5786

CMMA

5-Me-AMT

iso-DMT

6-Et-T

1-Ethyltryptamine

1-Pentyl-7-azaindole

1-Pentyl-6-azaindole

1-Pentyl-5-azaindole

1-Pentyl-4-azaindole

7 Dec 2019 · · Isomer Design