Exploring pyr-T. To explore a different substance…

Names:
pyr-T
Pyrrolidyltryptamine
Tryptamine, N,N-tetramethylene
Indole, 3-[2-(1-pyrrolidyl)ethyl]
Pyrrolidine, 1-[2-(3-indolyl)ethyl]
N,N-Tetramethylenetryptamine
1-[2-(1H-Indol-3-yl)ethyl]pyrrolidine
1-[2-(1-Pyrrolidyl)ethyl]indole
IUPAC name:
3-[2-(Pyrrolidin-1-yl)ethyl]-1H-indole
5052 · C14H18N2 · 214.306
InChI=1S/C14H18N2/c1-2-6-14-13(5-1)12(11-15-14)7-10-16-8-3-4-9-16/h1-2,5-6,11,15H,3-4,7-10H2
CVTZCBLFHNGYDQ-UHFFFAOYSA-N This stereoisomer Any stereoisomer

McKenna, DJ; Repke, DB; Lo, L; Peroutka, SJ. Differential interactions of indolealkylamines with 5-hydroxytryptamine receptor subtypes. Neuropharmacology, 1 Mar 1990, 29 (3), 191–198. 679 kB. https://doi.org/10.1016/0028-3908(90)90001-8

Nichols, DE. Chemistry and structure–activity relationships of psychedelics. In Behavioral Neurobiology of Psychedelic Drugs; Halberstadt, AL; Vollenweider, FX; Nichols, DE, Eds., Springer, 1 Jan 2017; pp 1-43. 2.6 MB. https://doi.org/10.1007/7854_2017_475

Cami-Kobeci, G; Slatford, PA; Whittlesey, MK; Williams, JMJ. N-Alkylation of phenethylamine and tryptamine. Bioorg. Med. Chem. Lett., 1 Feb 2005, 15 (3), 535–537. 265 kB. https://doi.org/10.1016/j.bmcl.2004.11.050 #25

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.

MALT
2790
1-Ethyl-1-methyl-THβC
867
MCPT
SN-22
α-MT-NPI
WAY-163909
21 August 2018 · Creative Commons BY-NC-SA ·