Exploring MPM. To explore a different substance…

Names:
MPM
2,5-Dimethoxy-4-propoxyamphetamine
2,5-Dimethoxy-4-n-propoxyamphetamine
IUPAC name:
1-(2,5-Dimethoxy-4-propoxyphenyl)propan-2-amine
138 · C14H23NO3 · 253.337
InChI=1S/C14H23NO3/c1-5-6-18-14-9-12(16-3)11(7-10(2)15)8-13(14)17-4/h8-10H,5-7,15H2,1-4H3
YORRDSMCIGRARV-UHFFFAOYSA-N This stereoisomer Any stereoisomer

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

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.

Braun, U; Braun, G; Jacob, P; Nichols, DE; Shulgin, AT. Mescaline Analogs: Substitutions at the 4-Position. 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 27–37. 497 kB. Rhodium.

B
EEM
EME
MEE
TRIS
APM
Hydroxy-DOPR
MIPM
3C-P
3C-IP
2C-O-19
IB
4C-EtO
β-HO-2,5-DMIPA
β-HO-N-Me-2,5-DEA
I-TRIS
4C-HE
N,N-Me-TMA-2
N-Pr-M
2,4,6-TRIS
SBU · sec-Buscaline
TBU · tert-Buscaline
5983
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