• Molecular NameDicoumarol
  • SynonymBHC; Bis-Hydroxycoumarin; Bishydroxycoumarin; Dicoumarin; Dicoumarol
  • Weight336.299
  • Drugbank_IDDB00266
  • ACS_NO66-76-2
  • Show 2D model
  • LogP (experiment)2.07
  • LogP (predicted, AB/LogP v2.0)1.4
  • pka4.4, 8.0
  • LogD (pH=7, predicted)-0.59
  • Solubility (experiment)0.128 mg/ml
  • LogS (predicted, ACD/Labs)(ph=7)-2.62
  • LogSw (predicted, AB/LogsW2.0)0.07
  • Sw (mg/ml) (predicted, ACD/Labs)0.01
  • No.of HBond Donors2
  • No.of HBond Acceptors6
  • No.of Rotatable Bonds2
  • TPSA93.06
  • StatusFDA approved
  • AdministrationN/A
  • PharmacologyAn anticoagulant that functions as a Vitamin K antagonist (similar to warfarin). It is also used in biochemical experiments as an inhibitor of reductases. Dicoumarol is a chemical substance of plant origin, a derivative of coumarin.
  • Absorption_valueN/A
  • Absorption (description)N/A
  • Caco_2N/A
  • BioavailabilityN/A
  • Protein binding99.0
  • Volume of distribution (VD)N/A
  • Blood/Plasma Partitioning ratio (D_blood)N/A
  • Metabollsmplasmatic proteins
  • Half lifedose-dependent and may range from 7~100 h
  • Excretionfaeces, urine
  • Urinary ExcretionN/A
  • CleranceN/A
  • ToxicityN/A
  • LD50 (rat)LD50=250 mg/kg
  • LD50 (mouse)LD50=233 mg/kg