• Molecular NameAcetohydroxamic Acid
  • SynonymAcethydroxamsaure; Acetic acid; oxime; Acetohydroxamate; Acetohydroximic acid; Acetyl hydroxyamino; Acetylhydroxamic acid; AHA; Cetohyroxamic acid; Methylhydroxamic acid; N-Hydroxyacetamide
  • Weight75.067
  • Drugbank_IDDB00551
  • ACS_NO546-88-3
  • Show 2D model
  • LogP (experiment)-0.567
  • LogP (predicted, AB/LogP v2.0)-1.23
  • pka8.7
  • LogD (pH=7, predicted)-1.23
  • Solubility (experiment)N/A
  • LogS (predicted, ACD/Labs)(ph=7)1.12
  • LogSw (predicted, AB/LogsW2.0)258.88
  • Sw (mg/ml) (predicted, ACD/Labs)1000.0
  • No.of HBond Donors2
  • No.of HBond Acceptors3
  • No.of Rotatable Bonds0
  • TPSA49.33
  • StatusFDA approved
  • AdministrationN/A
  • PharmacologyA drug that is a potent and irreversible inhibitor of bacterial and plant urease usually used for urinary tract infections.
  • Absorption_valueN/A
  • Absorption (description)Well absorbed from the GI tract following oral administration.
  • Caco_2N/A
  • Bioavailability55.0
  • Protein bindingN/A
  • Volume of distribution (VD)N/A
  • Blood/Plasma Partitioning ratio (D_blood)N/A
  • Metabollsm35-65% of oral dose excreted unchanged in urine (which provides the drug's therapeutic effect).
  • Half life3.5~10 h
  • ExcretionApproximately 35–65% of an orally administered dose is excreted unchanged in urine within 24–48 hours in patients with normal renal function; less than 10% is excreted in urine as acetamide.
  • Urinary ExcretionN/A
  • CleranceN/A
  • ToxicityOral, rat: LD50 = 4.8gm/kg. Symptoms of overdose include anorexia, malaise, lethargy, diminished sense of wellbeing, tremor, anxiety, nausea, and vomiting.
  • LD50 (rat)N/A
  • LD50 (mouse)N/A