Edge Rewrite
// 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.

Jump to content

Clofluperol

From Wikipedia, the free encyclopedia

Clofluperol
Clinical data
Other namesSeperidol, R9298
Identifiers
  • 4-[4-[4-chloro-3-(trifluoromethyl)phenyl]-4-hydroxypiperidin-1-yl]-1-(4-fluorophenyl)butan-1-one
CAS Number
PubChem CID
ChemSpider
UNII
ChEMBL
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC22H22ClF4NO2
Molar mass443.87 g·mol−1
3D model (JSmol)
  • C1CN(CCC1(C2=CC(=C(C=C2)Cl)C(F)(F)F)O)CCCC(=O)C3=CC=C(C=C3)F
  • InChI=1S/C22H22ClF4NO2/c23-19-8-5-16(14-18(19)22(25,26)27)21(30)9-12-28(13-10-21)11-1-2-20(29)15-3-6-17(24)7-4-15/h3-8,14,30H,1-2,9-13H2
  • Key:LZFSKNPPWIFMFL-UHFFFAOYSA-N

Clofluperol is a neuroleptic tranquilizer of the butyrophenone class.[1][2][3] It has the same aromatic piperidinol moiety that is present in penfluridol and fluperamide. The structure can be seen to be a sort of hybrid between that of trifluperidol and haloperidol.

References

[edit]
  1. ↑ Bobon J, Pinchard A, Goffioul F, Devroye A, Bobon DP, Korn M (February 1968). "[Long-acting neuroleptics. I. Pilot study of clofluperol (R9298)]". Acta Neurologica et Psychiatrica Belgica (in French). 68 (2): 128–136. PMID 4972601.
  2. ↑ Janssen PA, Allewijn FT (February 1969). "The distribution of the butyrophenones haloperidol, trifluperidol, moperone, and clofluperol in rats, and its relationship with their neuroleptic activity". Arzneimittel-Forschung. 19 (2): 199–208. PMID 5818759.
  3. ↑ Mishkinsky J, Khazen K, Givant Y, Dikstein S (May 1969). "Sulman FG: Mammotropic and neuroleptic effects of butyrophenones in the rat". Archives Internationales de Pharmacodynamie et de Therapie. 179 (1): 94–105. PMID 5388566.