Cepentil

Last updated

Cepentil
LAcPe structure.png
Identifiers
  • N-cyclopentyl-7-methyl-6,6a,8,9-tetrahydro-4H-indolo[4,3-fg]quinoline-9-carboxamide
PubChem CID
ChemSpider
Chemical and physical data
Formula C21H25N3O
Molar mass 335.451 g·mol−1
3D model (JSmol)
  • CN1CC(C=C2C1CC3=CNC4=CC=CC2=C34)C(=O)NC5CCCC5
  • InChI=1S/C21H25N3O/c1-24-12-14(21(25)23-15-5-2-3-6-15)9-17-16-7-4-8-18-20(16)13(11-22-18)10-19(17)24/h4,7-9,11,14-15,19,22H,2-3,5-6,10,12H2,1H3,(H,23,25)
  • Key:GIUWLXABHBAKDK-UHFFFAOYSA-N

Cepentil (Tsepentil, N-Cyclopentyllysergamide, LCyP), is an analogue of LSD developed in the former Soviet Union which acts as an antagonist at serotonin receptors. It is not a hallucinogen in animal studies, instead being described as an "energizer" by contemporary sources, suggesting an action similar to the antidementia drug hydergine, however the pharmacology of cepentil has not been studied with modern techniques. [1] [2] [3] [4]

See also

References

  1. ↑ Votava Z, Podvalova I, Semonsky M (May 1958). "Studies on the pharmacology of D-lysergic acid cycloalkylamides". Archives Internationales de Pharmacodynamie et de Therapie. 115 (1–2): 114–30. PMID   13545891.
  2. ↑ Zakusov VV (January 1964). "Pharmacology and chemistry". Vestnik Akademii Meditsinskikh Nauk SSSR (in Russian). 19: 43–51. PMID   14203697.
  3. ↑ Usdin E, Efron DH (1972). Psychotropic Drugs and Related Compounds. National Institute of Mental Health. pp. 94–95. ASIN   B002X3CDIY.
  4. ↑ Sankar DV (1975). LSD - A Total Study. PJD Publications. pp. 150–152. ISBN   0-9600290-3-6.
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