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Cepentil

From Wikipedia, the free encyclopedia
(Redirected fromLysergic acid cyclopentylamide)

Pharmaceutical compound
Cepentil
Clinical data
Other namesTsepentil;N-Cyclopentyllysergamide; NCPe-LA;N-Cyclopentyl-lysergamide; LCyP; C5AL
Identifiers
  • N-cyclopentyl-7-methyl-6,6a,8,9-tetrahydro-4H-indolo[4,3-fg]quinoline-9-carboxamide
PubChemCID
ChemSpider
Chemical and physical data
FormulaC21H25N3O
Molar mass335.451 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, orTsepentil, also known asN-cyclopentyllysergamide (NCPe-LA) or aslysergic acid cyclopentylamide (LCyP), is ananalogue ofLSD developed in the formerSoviet Union which acts as anantagonist atserotonin receptors. It does not producehallucinogen-like effects inanimal studies, instead being described as an "energizer" by contemporary sources, suggesting an action similar to theantidementia drughydergine, however thepharmacology of cepentil has not been studied with modern techniques.[1][2][3][4]

See also

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References

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  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.

External links

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5-HT2C
5-HT37
5-HT3
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Ergolines
(incl.lysergines)
Clavines
(6,8-dimethylergolines)
Lysergamides
(lysergic acid amides)
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