Exploring PE. To explore a different substance…

Names:
PE
Phenescaline
3,5-Dimethoxy-4-phenethyloxyphenethylamine
IUPAC name:
2-[3,5-Dimethoxy-4-(2-phenylethoxy)phenyl]ethan-1-amine
141 · C18H23NO3 · 301.38
InChI=1S/C18H23NO3/c1-20-16-12-15(8-10-19)13-17(21-2)18(16)22-11-9-14-6-4-3-5-7-14/h3-7,12-13H,8-11,19H2,1-2H3
FKXBCTFKCKEDNI-UHFFFAOYSA-N This stereoisomer Any stereoisomer

Parker, MA; Kurrasch, DM; Nichols, DE. The role of lipophilicity in determining binding affinity and functional activity for 5-HT2A receptor ligands. Bioorg. Med. Chem., 1 Jan 2008, 16 (8), 4661–4669. 296 kB. https://doi.org/10.1016/j.bmc.2008.02.033

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.

Jacob, P; Shulgin, AT. Structure-activity relationships of the classic hallucinogens and their analogs. In Hallucinogens: An update. NIDA Research Monograph 146; Lin, GC; Glennon, RA, Eds., U.S. Department of Health and Human Services, National Institute of Health, U.S. Government Printing Office, Washington, DC, 1994; pp 74–91. 51 kB.

3C-BZ
DMPEA-NBOMe · 25H-NBOMe
24-NBOMe
MBZM
35-NBOMe
26-NBOMe
25D-NBOH
25H-NB3OMe
25H-NB4OMe
Isoxsuprine
3,4-DMA-NBOH
21 August 2018 · Creative Commons BY-NC-SA ·