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Chemical compound
ECPLA
Other names ECYPLA
Legal status
(6aR ,9R )-N -Cyclopropyl-N -ethyl-7-methyl-4,6,6a,7,8,9-hexahydroindolo[4,3-fg ]quinoline-9-carboxamide
Formula C 21 H 25 N 3 O
Molar mass 335.451 g·mol−1 3D model (
JSmol )
CCN(C1CC1)C(=O)[C@@H]3C=C2c4cccc5ncc(C[C@H]2N(C)C3)c45
InChI=1S/C21H25N3O/c1-3-24(15-7-8-15)21(25)14-9-17-16-5-4-6-18-20(16)13(11-22-18)10-19(17)23(2)12-14/h4-6,9,11,14-15,19,22H,3,7-8,10,12H2,1-2H3/t14-,19-/m1/s1
Key:UNUJKEQFYPYXBK-AUUYWEPGSA-N
ECPLA (N -ethyl-N -cyclopropyllysergamide ) is an
analog of
lysergic acid diethylamide (LSD) developed by Synex Synthetics. In studies in mice, it was found to have approximately 40% the potency of LSD.
[2]
[3]
See also
References
^
"Arrêté du 20 mai 2021 modifiant l'arrêté du 22 février 1990 fixant la liste des substances classées comme stupéfiants" . www.legifrance.gouv.fr (in French). 20 May 2021.
^ Halberstadt AL, Klein LM, Chatha M, Valenzuela LB, Stratford A, Wallach J, et al. (February 2019).
"Pharmacological characterization of the LSD analog N-ethyl-N-cyclopropyl lysergamide (ECPLA)" . Psychopharmacology . 236 (2): 799–808.
doi :
10.1007/s00213-018-5055-9 .
PMC
6848745 .
PMID
30298278 .
^ Wagmann L, Richter LH, Kehl T, Wack F, Bergstrand MP, Brandt SD, et al. (July 2019).
"In vitro metabolic fate of nine LSD-based new psychoactive substances and their analytical detectability in different urinary screening procedures" (PDF) . Analytical and Bioanalytical Chemistry . 411 (19): 4751–4763.
doi :
10.1007/s00216-018-1558-9 .
PMID
30617391 .
S2CID
58615418 .
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