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ETFELA

From Wikipedia, the free encyclopedia
(Redirected fromEthyltrifluoroethyllysergamide)
Chemical compound
Pharmaceutical compound
ETFELA
Clinical data
Other namesN-Ethyl-N-(2,2,2-trifluoroethyl)lysergamide; LA-CH2CF3
Drug classSerotonin receptor modulator
Identifiers
  • (6aR,9R)-N-Ethyl-7-methyl-N-(2,2,2-trifluoroethyl)-4,6,6a,7,8,9-hexahydroindolo[4,3-fg]quinoline-9-carboxamide
CAS Number
PubChemCID
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC20H22F3N3O
Molar mass377.411 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, also known asN-ethyl-N-(2,2,2-trifluoroethyl)lysergamide, is ananalogue oflysergic acid diethylamide (LSD) firstsynthesized by Jason C. Parrish as part of the research team led byDavid E. Nichols. In studiesin vitro, it was found to be slightly morepotent than LSD itself.[1][2]

Chemistry

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Analogues

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Analogues of ETFELA includeLSD,EcPLA,EiPLA,MiPLA,FLUORETH-LAD (FE-LAD), andFP-LAD, among others.

See also

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References

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  1. ^Nichols DE (2012)."Structure-activity relationships of serotonin 5-HT2A agonists".Wiley Interdisciplinary Reviews: Membrane Transport and Signaling.1 (5):559–579.doi:10.1002/wmts.42.
  2. ^Nichols DE (2017). "Chemistry and Structure-Activity Relationships of Psychedelics".Behavioral Neurobiology of Psychedelic Drugs. Current Topics in Behavioral Neurosciences. Vol. 36. pp. 1–43.doi:10.1007/7854_2017_475.ISBN 978-3-662-55878-2.PMID 28401524.S2CID 4396184.

External links

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