Exploring DOIP. To explore a different substance…

Names:
DOIP
2,5-Dimethoxy-4-isopropylamphetamine
IUPAC name:
1-[2,5-Dimethoxy-4-(propan-2-yl)phenyl]propan-2-amine
246 · C14H23NO2 · 237.338
InChI=1S/C14H23NO2/c1-9(2)12-8-13(16-4)11(6-10(3)15)7-14(12)17-5/h7-10H,6,15H2,1-5H3
SPKSLAUXKHSASF-UHFFFAOYSA-N This stereoisomer Any stereoisomer

Aldous, FAB; Barrass, BC; Brewster, K; Buxton, DA; Green, DM; Pinder, RM; Rich, P; Skeels, PM; Tutt, KJ. Structure-activity relationships in psychotomimetic phenylalkylamines. J. Med. Chem., 1 Oct 1974, 17 (10), 1100–1111. 1.2 MB. https://doi.org/10.1021/jm00256a016

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

Glennon, RA; Seggel, MR. Interaction of phenylisopropylamines with central 5-HT2 receptors. Analysis by quantitative structure-activity relationships. In Probing Bioactive Mechanisms; ACS Symposium Series; Magee, PS; Henry, DR; Block, JH, Eds., American Chemical Society, Washington, DC, 14 Nov 1989; Vol. 413, pp 264–280. 4.4 MB. https://doi.org/10.1021/bk-1989-0413.ch018

EMCDDA. New drugs in Europe, 2015, European Monitoring Centre for Drugs and Drug Addiction, 1 May 2016. 1.0 MB. #38

Brimblecombe, RW; Pinder, RM. Hallucinogenic agents, Wright-Scientechnica, Bristol, UK, 1 Jan 1975. 46.2 MB.

Shulgin, AT. Basic Pharmacology and Effects. In Hallucinogens. A Forensic Drug Handbook; Laing, R; Siegel, JA, Eds., Academic Press, London, 2003; pp 67–137. 6.3 MB.

DOPR
186
187
188
2101
2156
2157
4C-E
MO3MB
DMPA
N,N-Me-DEPEA
β,β-Me-DOM
N,N-Me-DOM
N-Et-DOM
α,β-Me-DOM
2C-IB
DOM-2,5-DIEtO
G-21
G-12
2C-G-22
525
530
531
532
1209
1210
4,3,5-DOPR
DOTMA
2C-TBU
METHYL-DOET
2C-BU
N-Pr-2,5-DMA
2,4-Dimethoxy-5-propylamphetamine
19 September 2018 · Creative Commons BY-NC-SA ·