• Molecular NameFlurbiprofen
  • SynonymFLP; Flurbiprofen Sodium; Flurbiprofene [INN-French]; Flurbiprofeno [INN-Spanish]; Flurbiprofenum [INN-Latin]
  • Weight244.265
  • Drugbank_IDDB00712
  • ACS_NO5104-49-4
  • Show 2D model
  • LogP (experiment)4.16
  • LogP (predicted, AB/LogP v2.0)3.95
  • pka4.2
  • LogD (pH=7, predicted)1.25
  • Solubility (experiment)0.008 mg/ml
  • LogS (predicted, ACD/Labs)(ph=7)-1.12
  • LogSw (predicted, AB/LogsW2.0)0.02
  • Sw (mg/ml) (predicted, ACD/Labs)0.06
  • No.of HBond Donors1
  • No.of HBond Acceptors2
  • No.of Rotatable Bonds3
  • TPSA37.3
  • StatusFDA approved
  • AdministrationN/A
  • PharmacologyA member of the phenylalkanoic acid derivative family of non-steroidal anti-inflammatory drugs (NSAIDs) used to treat the inflammation and pain of arthritis.
  • Absorption_value95.0
  • Absorption (description)Readily absorbed after oral administration.
  • Caco_2N/A
  • Bioavailability92.0
  • Protein binding99.5
  • Volume of distribution (VD)0.1 L/kg
  • Blood/Plasma Partitioning ratio (D_blood)N/A
  • MetabollsmHepatic (CYP2C9)
  • Half life3.5 h
  • ExcretionAbout 95% of a dose is excreted in the urine in 24 h, mainly as the 4′-hydroxy, 3′,4′-dihydroxy, and 4′-methoxy metabolites, which are excreted partly as conjugates; about 25% of a dose is excreted as unchanged drug.
  • Urinary ExcretionN/A
  • Clerance0.3 ml/min/kg
  • ToxicityN/A
  • LD50 (rat)N/A
  • LD50 (mouse)N/A