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Chemical compound
ETFELA
Other names LA-CH2 CF3
(6aR ,9R )-N -Ethyl-7-methyl-N -(2,2,2-trifluoroethyl)-4,6,6a,7,8,9-hexahydroindolo[4,3-fg ]quinoline-9-carboxamide
Formula C 20 H 22 F 3 N 3 O
Molar mass 377.411 g·mol−1 3D model (
JSmol )
CCN(C(=O)[C@H]1CN(C)[C@H]2C(=C1)c1cccc3c1c(C2)c[nH]3)CC(F)(F)F
InChI=1S/C20H22F3N3O/c1-3-26(11-20(21,22)23)19(27)13-7-15-14-5-4-6-16-18(14)12(9-24-16)8-17(15)25(2)10-13/h4-7,9,13,17,24H,3,8,10-11H2,1-2H3/t13-,17-/m1/s1
Key:VAHPXTJQSWECIC-CXAGYDPISA-N
ETFELA (N -ethyl-N -(2,2,2-trifluoroethyl)lysergamide ) is an
analog of
lysergic acid diethylamide (LSD) first synthesised by Jason C. Parrish as part of the research team led by
David E. Nichols . In studies
in vitro , it was found to be slightly more potent than LSD itself.
[1]
[2]
See also
References
Psychedelics (
5-HT2A agonists)
Benzofurans
Lyserg‐ amides
Phenethyl‐ amines
2C-x
25x -NBx
25x -
NB 25x -
NB3OMe 25x -
NB4OMe 25x -
NBF 25x -
NBMD 25x -
NBOH 25x -
NBOMe Atypical structures
25x -NMx
N-(2C)-fentanyl
3C-x 4C-x
DOx HOT-x
MDxx Mescaline (subst.)
TMAs
TMA
TMA-2
TMA-3
TMA-4
TMA-5
TMA-6
Others
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alpha -alkyltryptamines x -
DALT x -
DET x -
DiPT x -
DMT
4,5-DHP-DMT
2,N,N-TMT
4-AcO-DMT
4-HO-5-MeO-DMT
4,N,N-TMT
4-Propionyloxy-DMT
5,6-diBr-DMT
5-AcO-DMT
5-Bromo-DMT
5-MeO-2,N ,N -TMT
5-MeO-4,N ,N -TMT
5-MeO-α,N,N-TMT
5-MeO-DMT
5-N ,N -TMT
7,N,N-TMT
α,N,N-TMT
(Bufotenin) 5-HO-DMT
DMT
Norbaeocystin
(Psilocin) 4-HO-DMT
(Psilocybin) 4-PO-DMT
x -
DPT Ibogaine-related x -
MET x -
MiPT Others
Others
Dissociatives (
NMDAR
antagonists )
Deliriants (
mAChR
antagonists ) Others