Exploring DOCA. To explore a different substance…

Names:
DOCA
4-Carboxy-2,5-dimethoxyamphetamine
IUPAC name:
4-(2-Aminopropyl)-2,5-dimethoxybenzoic acid
2415 · C12H17NO4 · 239.268
InChI=1S/C12H17NO4/c1-7(13)4-8-5-11(17-3)9(12(14)15)6-10(8)16-2/h5-7H,4,13H2,1-3H3,(H,14,15)
FRWTXPXOPHGXDE-UHFFFAOYSA-N This stereoisomer Any stereoisomer

Seggel, MR; Yousif, MY; Lyon, RA; Titeler, M; Roth, BL; Suba, EA; Glennon, RA. A structure-affinity study of the binding of 4-substituted analogues of 1-(2,5-dimethoxyphenyl)-2-aminopropane at 5-HT2 serotonin receptors. J. Med. Chem., 1 Mar 1990, 33 (3), 1032–1036. 807 kB. https://doi.org/10.1021/jm00165a023

Ho, B; Estevez, V; Tansey, LW; Englert, LF; Creaven, PJ; McIsaac, WM. Analogs of amphetamine. 5. Excretory metabolites of 1-(2,5-dimethoxy-4-methylphenyl)-2-aminopropane (DOM) in rats. J. Med. Chem., 1 Feb 1971, 14 (2), 158–160. 371 kB. https://doi.org/10.1021/jm00284a019

Ho, B; Tansey, LW. Analogs of amphetamine. 4. Synthesis of metabolites of 1-(2,5-dimethoxy-4-methylphenyl)-2-aminopropane (DOM). J. Med. Chem., 1 Feb 1971, 14 (2), 156–157. 316 kB. https://doi.org/10.1021/jm00284a018

DMMDA
DMMDA-2
N-Acetyl-3-demethymescaline
N-Formylmescaline
N-Me,CHO-DME
N-Me-2C-DMMDA-3
DMMDA-3
N-Me-2C-DMMDA
N-Me-2C-DMMDA-2
DMMDA-5
DMMDA-4
DMMDA-6
α-Carboxy-2C-D
739
21 August 2018 · Creative Commons BY-NC-SA ·