Exploring 4,5-MDO-DMT. To explore a different substance…

Names:
4,5-MDO-DMT · N,N-Dimethyl-4,5-methylenedioxytryptamine · Tryptamine, N,N-dimethyl-4,5-methylenedioxy · Indole, 3-[2-(dimethylamino)ethyl]-4,5-methylenedioxy · 3-[2-(Dimethylamino)ethyl]-4,5-methylenedioxyindole · 5H-1,3-Dioxolo-[4,5-e]indole-7-ethanamine, N,N-dimethyl
IUPAC names:
2-(2H,6H-[1,3]Dioxolo[4,5-e]indol-8-yl)-N,N-dimethylethan-1-amine
2-(6H-[1,3]Dioxolo[4,5-e]indol-8-yl)-N,N-dimethylethan-1-amine
ID: 5030 · Formula: C13H16N2O2 · Molecular weight: 232.278
InChI: InChI=1S/C13H16N2O2/c1-15(2)6-5-9-7-14-10-3-4-11-13(12(9)10)17-8-16-11/h3-4,7,14H,5-6,8H2,1-2H3

Kline, TB; Benington, F; Morin, RD; Beaton, JM. Structure-activity relationships in potentially hallucinogenic N,N-dialkyltryptamines substituted in the benzene moiety. J. Med. Chem., 1 Jan 1982, 25 (8), 908–913. 845 kB. http://dx.doi.org/10.1021/jm00350a005

Kline, TB; Benington, F; Morin, RD; Beaton, JM; Glennon, RA; Domelsmith, LN; Houk, KN; Rozeboom, MD. Structure-activity relationships for hallucinogenic N,N-dialkyltryptamines: photoelectron spectra and serotonin receptor affinities of methylthio and methylenedioxy derivatives. J. Med. Chem., 1 Jan 1982, 25 (11), 1381–1383. 378 kB. http://dx.doi.org/10.1021/jm00353a021

4,5-MDO-DIPT
4,5-DHP-DMT
5,6-MDO-DMT
Melatonin
5-Formylpsilocin
7-Formylpsilocin
5750
5899
4,5-MDO-DIPT
4,5-DHP-DMT
5,6-MDO-DMT
Melatonin
5-Formylpsilocin
7-Formylpsilocin
5750
5899
24 November 2017 · Creative Commons BY-NC-SA ·