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EiPLA

From Wikipedia, the free encyclopedia
Chemical compound

Pharmaceutical compound
EiPLA
Clinical data
Other namesEiPLA; Ethylisopropyllysergamide;N-Ethyl-N-isopropyllysergamide; Lysergic acid ethylisopropylamide
Routes of
administration
Oral
Drug classSerotonin receptor modulator;Serotonin 5-HT2A receptor agonist;Serotonergic psychedelic;Hallucinogen
Legal status
Legal status
Identifiers
  • (6aR,9R)-N-ethyl-7-methyl-N-propan-2-yl-6,6a,8,9-tetrahydro-4H-indolo[4,3-fg]quinoline-9-carboxamide
CAS Number
PubChemCID
Chemical and physical data
FormulaC21H27N3O
Molar mass337.467 g·mol−1
3D model (JSmol)
  • CCN(C(C)C)C(=O)[C@H]1CN([C@@H]2CC3=CNC4=CC=CC(=C34)C2=C1)C
  • InChI=1S/C21H27N3O/c1-5-24(13(2)3)21(25)15-9-17-16-7-6-8-18-20(16)14(11-22-18)10-19(17)23(4)12-15/h6-9,11,13,15,19,22H,5,10,12H2,1-4H3/t15-,19-/m1/s1
  • Key:JLPRDEGOBAGMHN-DNVCBOLYSA-N

EiPLA, also known asN-ethyl-N-isopropyllysergamide or aslysergic acid ethylisopropylamide, is apsychedelic drug of thelysergamide family related tolysergic acid diethylamide (LSD).[1][2][3] It is anisomer ofETH-LAD.[3]

Interactions

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See also:Psychedelic drug § Interactions, andTrip killer § Serotonergic psychedelic antidotes

Pharmacology

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Pharmacodynamics

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Indrug discrimination tests in rodents, EiPLA was found to have approximately half thepotency ofLSD.[1][2][3]

Chemistry

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Analogues

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Analogues of EiPLA includeMiPLA,LAMPA (MPLA),EPLA,EcPLA, andETFELA, among others.

History

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EiPLA was first described in thescientific literature byDavid E. Nichols and colleagues by at least 1994.[1] It appears to have emerged as a noveldesigner drug by 2019.[3]

See also

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References

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  1. ^abcHuang X, Marona-Lewicka D, Pfaff RC, Nichols DE (March 1994). "Drug discrimination and receptor binding studies of N-isopropyl lysergamide derivatives".Pharmacology, Biochemistry, and Behavior.47 (3):667–673.doi:10.1016/0091-3057(94)90172-4.PMID 8208787.
  2. ^abNichols DE (October 2018). "Dark Classics in Chemical Neuroscience: Lysergic Acid Diethylamide (LSD)".ACS Chemical Neuroscience.9 (10):2331–2343.doi:10.1021/acschemneuro.8b00043.PMID 29461039.
  3. ^abcdBrandt SD, Kavanagh PV, Westphal F, Pulver B, Schwelm HM, Stratford A, et al. (February 2024). "Analytical and behavioral characterization of N-ethyl-N-isopropyllysergamide (EIPLA), an isomer of N6 -ethylnorlysergic acid N,N-diethylamide (ETH-LAD)".Drug Testing and Analysis.16 (2):187–198.doi:10.1002/dta.3530.PMID 37321559.

External links

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