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Exploring MPPP (opioid). To explore a different substance…

Names

MPPP (opioid)
Desmethylprodine
1-Methyl-4-phenyl-4-propionoxypiperidine
R-1143

IUPAC name

1-Methyl-4-phenylpiperidin-4-yl propanoate

ID 5451 · Formula C₁₅H₂₁NO₂ · Molecular weight 247.333

InChI InChI=1S/C15H21NO2/c1-3-14(17)18-15(9-11-16(2)12-10-15)13-7-5-4-6-8-13/h4-8H,3,9-12H2,1-2H3

InChI Key BCQMRZRAWHNSBF-UHFFFAOYSA-N This stereoisomer Any stereoisomer

SMILES CCC(=O)OC1(CCN(CC1)C)c1ccccc1

ChemSpider 55493
PubChem 61583
Wikidata Q408952
Wikipedia Desmethylprodine

TiHKAL #14 Harmine

Phenethylamine: Von der Strucktur zur Funktion MPPP (opioid): 3.12 (81) 246

Ziporyn, T. A growing industry and menace: Makeshift laboratory’s designer drugs. JAMA, 12 Dec 1986, 256 (22), 3061–3063. 486 kB. https://doi.org/10.1001/jama.1986.03380220011003

Janssen, PAJ; Eddy, NB. Compounds related to pethidine--IV. New general chemical methods of increasing the analgesic activity of pethidine. J. Med. Chem., 1 Feb 1960, 2 (1), 31–45. 520 kB. https://doi.org/10.1021/jm50008a003 #R-1143

Harper, NJ; Simmonds, AB. Flurocompounds related to the reversed esters of pethidine. J. Med. Chem., 1 Apr 1959, 1 (2), 181–185. 291 kB. https://doi.org/10.1021/jm50003a006 #22

Passie, T; Brandt, SD. Self-experiments with psychoactive substances: A historical perspective. In New Psychoactive Substances: Pharmacology, Clinical, Forensic and Analytical Toxicology; Maurer, HH; Brandt, SD, Eds., Springer, Berlin, Heidelberg, 1 Jan 2018; pp 69-110. 563 kB. https://doi.org/10.1007/164_2018_177 #MPPP

2C-G-5

Meperidine

4-MeO-α-PBP

2C-D-butterFLY

ED-pyr-A

H-MOTH · PLY

EPH · Ethylphenidate

O-2418

2770

4-Me-MPH · 4-Methylmethylphenidate

3-MeO-2′-Oxo-PCE · MXE · Methoxetamine

3-Methylmethylphenidate

Ketobemidone

3,4-MD-PCE

9646

US4291059

3-Methoxy-PPPO

N-Cyclopentyl-3-methoxycathinone

N,N-Dimethyl-2C-D-FLY

11324

13003

7 Dec 2019 · · Isomer Design