Jump to content

Phenindione

From Wikipedia, the free encyclopedia

This is an old revision of this page, as edited by Jytdog (talk | contribs) at 19:57, 31 October 2016 (Undid revision 747146358 by 92.10.156.244 (talk) unsourced). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

Phenindione
Clinical data
AHFS/Drugs.comInternational Drug Names
Pregnancy
category
Routes of
administration
Oral
ATC code
Pharmacokinetic data
Protein binding88%
Elimination half-life5 to 10 hours
Identifiers
  • 2-phenyl-1H-indene-1,3(2H)-dione
CAS Number
PubChem CID
IUPHAR/BPS
DrugBank
ChemSpider
UNII
KEGG
ChEBI
ChEMBL
CompTox Dashboard (EPA)
ECHA InfoCard100.001.323 Edit this at Wikidata
Chemical and physical data
FormulaC15H10O2
Molar mass222.239 g/mol g·mol−1
3D model (JSmol)
  • O=C2c1ccccc1C(=O)C2c3ccccc3
  • InChI=1S/C15H10O2/c16-14-11-8-4-5-9-12(11)15(17)13(14)10-6-2-1-3-7-10/h1-9,13H checkY
  • Key:NFBAXHOPROOJAW-UHFFFAOYSA-N checkY
  (verify)

Phenindione is an anticoagulant which functions as a Vitamin K antagonist.

Hypersensitivity has been observed.[1]

References

  1. ^ Naisbitt DJ; Farrell J; Chamberlain PJ; et al. (June 2005). "Characterization of the T-cell response in a patient with phenindione hypersensitivity". J. Pharmacol. Exp. Ther. 313 (3): 1058–65. doi:10.1124/jpet.105.083758. PMID 15743920. {{cite journal}}: Unknown parameter |name-list-format= ignored (|name-list-style= suggested) (help)