• Molecular NameLomustine
  • SynonymCCNU; Chloroethylcyclohexylnitrosourea; Lomustina [INN-Spanish]; Lomustinum [INN-Latin]
  • Weight233.699
  • Drugbank_IDDB01206
  • ACS_NO13010-47-4
  • Show 2D model
  • LogP (experiment)2.629
  • LogP (predicted, AB/LogP v2.0)2.51
  • pkaN/A
  • LogD (pH=7, predicted)2.51
  • Solubility (experiment)0.111 mg/ml
  • LogS (predicted, ACD/Labs)(ph=7)-2.63
  • LogSw (predicted, AB/LogsW2.0)3.17
  • Sw (mg/ml) (predicted, ACD/Labs)0.55
  • No.of HBond Donors1
  • No.of HBond Acceptors5
  • No.of Rotatable Bonds4
  • TPSA61.77
  • StatusFDA approved
  • AdministrationN/A
  • PharmacologyAn alkylating nitrosourea compound used in chemotherapy. It is in the same family as streptozotocin.
  • Absorption_value100.0
  • Absorption (description)Well and rapidly absorbed from the gastrointestinal tract.
  • Caco_2N/A
  • BioavailabilityN/A
  • Protein binding50.0
  • Volume of distribution (VD)N/A
  • Blood/Plasma Partitioning ratio (D_blood)N/A
  • MetabollsmHepatic. Rapid and complete, with active metabolites.
  • Half life94 min, however the metabolites have a serum half-life of 16 to 48 hours.
  • ExcretionN/A
  • Urinary ExcretionN/A
  • CleranceN/A
  • ToxicityPulmonary toxicity has been reported at cumulative doses usually greater than 1,100 mg/m2. There is one report of pulmonary toxicity at a cumulative dose of only 600 mg. The onset of toxicity has varied from 6 months after initiation of therapy, to as late as 15 years after.
  • LD50 (rat)LD50=70 mg/kg
  • LD50 (mouse)LD50=30