Edge Rewrite
everything Source code View original
// HTMLRewriter · presentation

This page was redesigned at the edge.

Cloudflare fetched the original article and streamed it through HTMLRewriter to apply an entirely new visual system without rebuilding the source page.

// request.cf · coarse context

A page that knows where it met you.

Only coarse request metadata is shown. This demo does not display or persist visitor IP addresses.

Country
US
Cloudflare location
CMH
Connection
HTTP/2
Language
Not provided

Ray ID: a23f8913ff8c98f1

Jump to content

Cepentil

Add links
From Wikipedia, the free encyclopedia

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
PubChem CID
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, or Tsepentil, also known as N-cyclopentyllysergamide (NCPe-LA) or as lysergic acid cyclopentylamide (LCyP), is an analogue of LSD developed in the former Soviet Union which acts as an antagonist at serotonin receptors. It does not produce hallucinogen-like effects 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

[edit]

References

[edit]
  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.
[edit]
Retrieved from "https://en.wikipedia.org/w/index.php?title=Cepentil&oldid=1337923968"