• Molecular NameFurazolidone
  • SynonymNitrofurazolidone; Nitrofurazolidonum; USAF EA-1
  • Weight225.16
  • Drugbank_IDDB00614
  • ACS_NO67-45-8
  • Show 3D model
  • LogP (experiment)-0.05
  • LogP (predicted, AB/LogP v2.0)1.17
  • pkaN/A
  • LogD (pH=7, predicted)1.17
  • Solubility (experiment)0.04 mg/ml
  • LogS (predicted, ACD/Labs)(ph=7)-3.27
  • LogSw (predicted, AB/LogsW2.0)0.1
  • Sw (mg/ml) (predicted, ACD/Labs)0.12
  • No.of HBond Donors0
  • No.of HBond Acceptors8
  • No.of Rotatable Bonds3
  • TPSA103.87
  • StatusFDA approved
  • AdministrationN/A
  • PharmacologyAn antibacterial.
  • Absorption_valueN/A
  • Absorption (description)Radiolabeled drug studies indicate that furazolidone is well absorbed following oral administration
  • Caco_2N/A
  • BioavailabilityN/A
  • Protein bindingN/A
  • Volume of distribution (VD)N/A
  • Blood/Plasma Partitioning ratio (D_blood)N/A
  • MetabollsmFurazolidone is rapidly and extensively metabolized; the primary metabolic pathway identified begins with nitro-reduction to the aminofuran derivative. Two major metabolites are produced: 3-amino-2-oxazolidone (AOZ) or beta-hydroxyethylhydrazine (HEH). AOZ is responsible for monoamine oxidase inhibition. Detoxification and elimination of the drug is done primarily by conjugation with glutathione.
  • Half life10 min
  • ExcretionN/A
  • Urinary ExcretionN/A
  • CleranceN/A
  • ToxicityReactions to Furoxone have been reported including a fall in blood pressure, urticaria, fever, arthralgia, and a vesicular morbilliform rash. Other adverse effects can include a brown discoloration of the urine; hemolysis can occur in G6PDH-deficient patients. The drug has a monoamine oxidase (MAO) inhibitory effect and should never be given concurrently to individuals already taking MAO inhibitors.
  • LD50 (rat)N/A
  • LD50 (mouse)LD50=1807 (peroral)