Exploring 2,5-DES-Me-DOM. To explore a different substance…

Name:
2,5-DES-Me-DOM
IUPAC name:
2-(2-Aminopropyl)-5-methylbenzene-1,4-diol
7109 · C10H15NO2 · 181.232
InChI=1S/C10H15NO2/c1-6-3-10(13)8(4-7(2)11)5-9(6)12/h3,5,7,12-13H,4,11H2,1-2H3
ISJCIACBPBDNKH-UHFFFAOYSA-N This stereoisomer Any stereoisomer

White, TJ; Goodman, D; Shulgin, AT; Castagnoli, N; Lee, R; Petrakis, NL. Mutagenic activity of some centrally active aromatic amines in Salmonella typhimurium. Mutat. Res., 1 Jan 1977, 56 (2), 199–202. 256 kB. https://doi.org/10.1016/0027-5107(77)90210-X

Jacob, P; Kline, TB; Castagnoli, N. Chemical and biological studies of 1-(2,5-dihydroxy-4-methylphenyl)-2-aminopropane, an analog of 6-hydroxydopamine. J. Med. Chem., 1 Jun 1979, 22 (6), 662–671. 1.4 MB. https://doi.org/10.1021/jm00192a011

Shulgin, AT. Hallucinogens. In Burger’s Medicinal Chemistry, 4th ed., Part III; Wolff, ME, Ed., Wiley & Co., 1981; pp 1109–1137. 4.7 MB. #17

Anderson, GM; Castagnoli, N; Kollman, PA. Quantitative structure-activity relationships in the 2,4,5-ring-substituted phenylisopropylamines. In QuaSAR: Quantitative Structure Activity Relationships of Analgesics, Narcotic Antagonists, and Hallucinogens. NIDA Research Monograph 22; Barnett, G; Trsic, M; Willette, RE, Eds., U.S. Department of Health and Human Services, National Institute of Health, U.S. Government Printing Office, Washington, DC, 1978; pp 199–217. 623 kB. #15

2C-H
3,4-DMPEA · DMPEA
N-Me-GEA
2,4-DMPEA
β-HO-PMA · 4-Methoxynorephedrine
2,3-DMPEA
2,6-DMPEA
3,5-DMPEA
MHA
BO3M
β-HO-Hordenine
β-MeO-HMePEA
β-HO-HMA · Oxilofrine
β,4-DMPEA
N-HO-PMA
N,N-Me-2,3-DHPEA
β,2-MHPEA-3
2,4-HMA
N,N-Me-DHPEA · N,N-Dimethyldopamine
N-Et-DHPEA
3,4-HHMA
DH-α-Et-PEA
β-Me-GEA
N-Me-HMPEA
HMA
β,2-HO-5,N-MePEA
β,2-HO-5-MeA
β-HO-2-M-5-MePEA
2,5-HMA
597
5HMA
HMA
m-Hydroxyephedrine
Etilefrine
748
12414
21 August 2018 · Creative Commons BY-NC-SA ·