Exploring LPD-824. To explore a different substance…

Names:
LA-Pyr
LPD-824
Lysergic acid pyrrolidide
N-Pyrrolidyllysergamide
IUPAC name:
[(8β)-6-Methyl-9,10-didehydroergolin-8-yl)](pyrrolidin-1-yl)methanone
ID: 5335 · Formula: C20H23N3O · Molecular weight: 321.416
InChI: InChI=1S/C20H23N3O/c1-22-12-14(20(24)23-7-2-3-8-23)9-16-15-5-4-6-17-19(15)13(11-21-17)10-18(16)22/h4-6,9,11,14,18,21H,2-3,7-8,10,12H2,1H3/t14-,18-/m1/s1
InChI Key: SETDYMMXQQXCRP-RDTXWAMCSA-NThis stereoisomerAny stereoisomer

Abramson, HA. Lysergic acid diethylamide (LSD-25) XXXI. Comparison by questionnaire of psychotomimetic activity of congeners on normal subjects and drug addicts. Br. J. Psychiatry, 1 Jul 1960, 106 (444), 1120–1123. 425 kB. https://doi.org/10.1192/bjp.106.444.1120

Oberlender, R; Pfaff, RC; Johnson, MP; Huang, X; Nichols, DE. Stereoselective LSD-like activity in d-lysergic acid amides of R- and S-2-aminobutane. J. Med. Chem., 1 Jan 1992, 35 (2), 203–211. 1.1 MB. https://doi.org/10.1021/jm00080a001

Parrish, JC. Toward a molecular understanding of hallucinogen action. Ph. D. Thesis, Purdue University, West Lafayette, IN, 1 Jan 2006. 5.5 MB.

Nichols, DE. Structure-activity relationships of serotonin 5-HT2A agonists. WIREs Membr. Transp. Signal, 1 Sep 2012, 1 (5), 559-579. 573 kB. https://doi.org/10.1002/wmts.42

Nichols, DE. LSD and its lysergamide cousins. In Heffter Review; Nichols, DE, Ed., Heffter Research Institute, Santa Fe, NM, 2001; Vol. 2, pp 80–87. 270 kB.

LA-Aziridine
LA-RR-Aziridine
LA-RS-Aziridine
LA-SS-Aziridine
N-Cyclobutyllysergamide
BENZYL-PINACA
SGT-185
26 May 2018 · Creative Commons BY-NC-SA ·