• Molecular NameOlanzapine
  • Synonymolanzapine
  • Weight312.441
  • Drugbank_IDDB00334
  • ACS_NO132539-06-1
  • Show 2D model
  • LogP (experiment)3.0
  • LogP (predicted, AB/LogP v2.0)2.73
  • pka5.0,7.4
  • LogD (pH=7, predicted)1.87
  • Solubility (experiment)Insoluble
  • LogS (predicted, ACD/Labs)(ph=7)-2.67
  • LogSw (predicted, AB/LogsW2.0)0.74
  • Sw (mg/ml) (predicted, ACD/Labs)0.06
  • No.of HBond Donors1
  • No.of HBond Acceptors4
  • No.of Rotatable Bonds1
  • TPSA59.11
  • StatusFDA approved
  • Administrationoral, intramuscular
  • PharmacologyAn atypical antipsychotic, approved by the FDA for the treatment of schizophrenia and bipolar disorder.
  • Absorption_value100.0
  • Absorption (description)Well absorbed, with approximately 40% of the dose metabolized before reaching the systemic circulation.
  • Caco_2N/A
  • Bioavailability60.0
  • Protein binding93.0
  • Volume of distribution (VD)16.4 L/kg
  • Blood/Plasma Partitioning ratio (D_blood)N/A
  • MetabollsmHepatic (direct glucuronidation and CYP mediated oxidation)
  • Half life33.1 h
  • Excretionurine 57%, feces 30%
  • Urinary Excretion7.3
  • Clerance6.2 ml/min/kg
  • ToxicityThe most commonly observed adverse events associated with the use of oral olanzapine (incidence of 5% or greater) and not observed at an equivalent incidence among placebo-treated patients (olanzapine incidence at least twice that for placebo) were: for schizofrenia - postural hypotension, constipation, weight gain, personality disorder (the term for designating non-aggressive objectionable behavior), akathisia; for bipolar mania - asthenia, dry mouth, constipation, dyspepsia, increased appetite, somnolence, dizziness, tremor.
  • LD50 (rat)N/A
  • LD50 (mouse)N/A