• Molecular NameMeclofenamic acid
  • SynonymAcide meclofenamique [INN-French]; Acido meclofenamico [INN-Spanish]; Acidum meclofenamicum [INN-Latin]; Meclofenamate; Meclomen (free acid); Meclophenamic acid
  • Weight296.153
  • Drugbank_IDDB00939
  • ACS_NO644-62-2
  • Show 3D model
  • LogP (experiment)6.0
  • LogP (predicted, AB/LogP v2.0)5.64
  • pka3.7
  • LogD (pH=7, predicted)2.57
  • Solubility (experiment)0.03 mg/ml
  • LogS (predicted, ACD/Labs)(ph=7)-2.71
  • LogSw (predicted, AB/LogsW2.0)0.01
  • Sw (mg/ml) (predicted, ACD/Labs)0.01
  • No.of HBond Donors2
  • No.of HBond Acceptors3
  • No.of Rotatable Bonds3
  • TPSA49.33
  • StatusFDA approved
  • AdministrationN/A
  • PharmacologyA drug used for joint and muscular pain.
  • Absorption_value100.0
  • Absorption (description)N/A
  • Caco_2N/A
  • Bioavailability65.1
  • Protein binding99.0
  • Volume of distribution (VD)N/A
  • Blood/Plasma Partitioning ratio (D_blood)N/A
  • MetabollsmHepatic. Meclofenamate is extensively metabolized to an active metabolite (Metabolite I; 3-hydroxymethyl metabolite of meclofenamate) and at least six other less well characterized minor metabolites. Only this Metabolite I has been shown in vitro to inhibit cyclooxygenase activity with approximately one fifth the activity of meclofenamate.
  • Half lifeN/A
  • ExcretionN/A
  • Urinary ExcretionN/A
  • CleranceN/A
  • ToxicityThe most frequently reported adverse reactions associated with meclofenamate sodium involve the gastrointestinal system and include diarrhea (10% to 33%), nausea with or without vomiting (11%), other gastrointestinal disorders (10%), and abdominal pain. Other reactions less frequently reported were pyrosis, flatulence, anorexia, constipation, stomatitis, and peptic ulcer. Edema, rash, urticaria, pruritus, headache, dizziness, tinnitus have also been reported.
  • LD50 (rat)N/A
  • LD50 (mouse)N/A