Exploring 5-AcO-DMT. To explore a different substance…

Names:
5-AcO-DMT · 5-Acetoxy-N,N-dimethyltryptamine
IUPAC name:
3-[2-(Dimethylamino)ethyl]-1H-indol-5-yl acetate
ID: 5132 · Formula: C14H18N2O2 · Molecular weight: 246.305
InChI: InChI=1S/C14H18N2O2/c1-10(17)18-12-4-5-14-13(8-12)11(9-15-14)6-7-16(2)3/h4-5,8-9,15H,6-7H2,1-3H3

Gessner, PK; Godse, DD; Krull, AH; McMullan, JM. Structure-activity relationships among 5-methoxy-N:N-dimethyltryptamine, 4-hydroxy-N:N-dimethyltryptamine (psilocin) and other substituted tryptamines. Life Sci., 1 Mar 1968, 7 (5), 267–277. 362 kB. http://dx.doi.org/10.1016/0024-3205(68)90200-2

Glennon, RA; Gessner, PK. Serotonin receptor binding affinities of tryptamine analogues. J. Med. Chem., 1 Jan 1979, 22 (4), pp 428–432. 731 kB. http://dx.doi.org/10.1021/jm00190a014

Glennon, RA; Hong, S; Bondarev, M; Law, H; Dukat, M; Rakhit, S; Power, P; Fan, E; Kinneau, D; Kamboj, R; Teitler, M; Herrick-Davis, K; Smith, C. Binding of O-alkyl derivatives of serotonin at human 5-HT1Dβ receptors. J. Med. Chem., 5 Jan 1996, 39 (1), 314–322. 193 kB. http://dx.doi.org/10.1021/jm950498t

DMT
5-HO-DMT
5-MeO-DMT
5-MeS-DMT
5-Br-DMT
Bufoviridine
5-EtO-DMT
5,N,N-TMT
Sumatriptan
5-F-DMT
5-Et-DMT
5-Chloro-DMT
5-TMS-DMT
5-Ac-DMT
5-Cam-DMT
4-HO-mor-T
4-AcO-DMT
5650
5751
5787
DMT
5-HO-DMT
5-MeO-DMT
5-MeS-DMT
5-Br-DMT
Bufoviridine
5-EtO-DMT
5,N,N-TMT
Sumatriptan
5-F-DMT
5-Et-DMT
5-Chloro-DMT
5-TMS-DMT
5-Ac-DMT
5-Cam-DMT
4-HO-mor-T
4-AcO-DMT
5650
5751
5787
10 December 2016 · Creative Commons BY-NC-SA ·