Exploring TA. To explore a different substance…

Names:
TA · 2,3,4,5-Tetramethoxyamphetamine
IUPAC name:
1-(2,3,4,5-Tetramethoxyphenyl)propan-2-amine
ID: 145 · Formula: C13H21NO4 · Molecular weight: 255.31
InChI: InChI=1S/C13H21NO4/c1-8(14)6-9-7-10(15-2)12(17-4)13(18-5)11(9)16-3/h7-8H,6,14H2,1-5H3

Shulgin, AT. Psychotomimetic drugs: structure-activity relationships. In Handbook of Psychopharmacology: Stimulants; Iversen, LL; Iversen, SD; Snyder, SH, Eds., Plenum Press, New York, 1978; Vol. 11, pp 243–333. 2.6 MB. http://dx.doi.org/10.1007/978-1-4757-0510-2_6 Rhodium.

Antun, F; Smythies, JR; Benington, F; Morin, RD; Barfknecht, CF; Nichols, DE. Native fluorescence and hallucinogenic potency of some amphetamines. Experientia, 15 Jan 1971, 27 (1), 62–63. 248 kB. http://dx.doi.org/10.1007/BF02137743

Thakur, M; Thakur, A; Khadikar, PV. QSAR studies on psychotomimetic phenylalkylamines. Bioorg. Med. Chem., 15 Feb 2004, 12 (4), 825–831. 323 kB. http://dx.doi.org/10.1016/j.bmc.2003.10.027

Altun, A; Golcuk, K; Kumru, M; Jalbout, AF. Electron-conformation study for the structure-hallucinogenic activity relationships of phenylalkylamines. Bioorg. Med. Chem., 1 Dec 2003, 11 (24), 3861–3868. 577 kB. http://dx.doi.org/10.1016/S0968-0896(03)00437-1

Shulgin, AT; Sargent, T; Naranjo, C. Structure-activity relationships of one-ring psychotomimetics. Nature, 1 Jan 1969, 221, 537–541. 537 kB. http://dx.doi.org/10.1038/221537a0

Shulgin, AT. Chemistry and structure-activity relationships of the psychotomimetics. In Psychotomimetic Drugs; Efron, DH, Ed., Raven Press, New York, 1970; pp 21–41. 8.6 MB.

TeMA
TeMPEA
TMA
2-I-TMA
TMA-2
TMA-4
TMA-3
5-I-TMA-3
PeMA
DMMDA-3
DMMDA
G-3
G-4
G-5
G-N
G-2
G-1
G-6
DMMDA-2
1081
1082
1083
266
341
TeMA-2
TeMA-3
1352
TeMA
TeMPEA
TMA
2-I-TMA
TMA-2
TMA-4
TMA-3
5-I-TMA-3
PeMA
DMMDA-3
DMMDA
G-3
G-4
G-5
G-N
G-2
G-1
G-6
DMMDA-2
1081
1082
1083
266
341
TeMA-2
TeMA-3
1352
21 September 2017 · Creative Commons BY-NC-SA ·