Exploring N-Heptan-2-yllysergamide. To explore a different substance…

Name:
N-Heptan-2-yllysergamide
IUPAC name:
(8β)-N-(Heptan-2-yl)-6-methyl-9,10-didehydroergoline-8-carboxamide
ID: 5323 · Formula: C23H31N3O · Molecular weight: 365.512
InChI: InChI=1S/C23H31N3O/c1-4-5-6-8-15(2)25-23(27)17-11-19-18-9-7-10-20-22(18)16(13-24-20)12-21(19)26(3)14-17/h7,9-11,13,15,17,21,24H,4-6,8,12,14H2,1-3H3,(H,25,27)/t15?,17-,21-/m1/s1
InChI Key: HTJZHVCGODLWLI-NZAAYYPMSA-NThis stereoisomerAny stereoisomer

Nichols, DE; Monte, A; Huang, X; Marona-Lewicka, D. Stereoselective pharmacological effects of lysergic acid amides possessing chirality in the amide substituent. Behav. Brain Sci., 15 Dec 1995, 73 (1–2), 117–119. 267 kB. https://doi.org/10.1016/0166-4328(96)00080-0

Monte, AP; Marona-Lewicka, D; Kanthasamy, A; Sanders-Bush, E; Nichols, DE. Stereoselective LSD-like activity in a series of d-lysergic acid amides of (R)- and (S)-2-aminoalkanes. J. Med. Chem., 1 Jan 1995, 38 (6), 958–966. 1.2 MB. https://doi.org/10.1021/jm00006a015

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.

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

N-Heptyllysergamide
BU-LAD
US 7772227 #12B
2AD-APINACA
APINACA
(2H-indazole) APINACA
24 May 2018 · Creative Commons BY-NC-SA ·