Exploring Mescaline-NBOMe. To explore a different substance…

Names:
M-NBOMe
Mescaline-NBOMe
NBOMe-mescaline
3,4,5-Trimethoxy-N-(2-methoxybenzyl)phenethylamine
N-(2-Methoxybenzyl)-3,4,5-trimethoxyphenethylamine
IUPAC names:
N-[(2-Methoxyphenyl)methyl]-2-(3,4,5-trimethoxyphenyl)ethan-1-amine
N-(2-Methoxybenzyl)-2-(3,4,5-trimethoxyphenyl)ethan-1-amine
403 · C19H25NO4 · 331.406
InChI=1S/C19H25NO4/c1-21-16-8-6-5-7-15(16)13-20-10-9-14-11-17(22-2)19(24-4)18(12-14)23-3/h5-8,11-12,20H,9-10,13H2,1-4H3
USPSMWCGHVXKMN-UHFFFAOYSA-N This stereoisomer Any stereoisomer

Anon. JW, Personal communication of unpublished research. 1 Dec 2011.

Pertz, H; Rheineck, A; Elz, S. N-Benzylated derivatives of the hallucinogenic drugs mescaline and escaline as partial agonists at rat vascular 5-HT2A receptors. N-S. Arch. Pharmacol., 1999, 359 (Suppl. 3), R29. 104 kB.

Chapman, SJ; Avanes, AA. PeakAL: Protons I Have Known and Loved — Fifty Shades of Grey-Market Spectra. BLOTTER, 1 Aug 2015, 1 (1). 2.6 MB. https://doi.org/10.16889/isomerdesign-1 Open access DOI

Chapman, SJ; Avanes, AA. PeakAL: Protons I Have Known and Loved — Fifty Shades of Grey-Market Spectra. Supplementary Data. BLOTTER, 1 Aug 2015, 1 (1). 11.9 MB. https://doi.org/10.16889/isomerdesign-1-supp Open access DOI

Rickli, A; Luethi, D; Reinisch, J; Buchy, D; Hoener, MC; Liechti, ME. Receptor interaction profiles of novel N-2-methoxybenzyl (NBOMe) derivatives of 2,5-dimethoxy-substituted phenethylamines (2C drugs). Neuropharmacology, 1 Dec 2015, 99 546–553. 625 kB. https://doi.org/10.1016/j.neuropharm.2015.08.034 #Mescaline-NBOMe

234-NBOMe
245-NBOMe
246-NBOMe
3,4-DMPEA-NB25OMe
20 September 2018 · Creative Commons BY-NC-SA ·