• Molecular NameChlorambucil
  • SynonymChlocambucil; Chloraminophen; Chloraminophene; Chlorbutin; Chlorbutine; Chloroambucil; Chlorobutin; Chlorobutine; Phenylbutyric Acid Nitrogen Mustard
  • Weight304.217
  • Drugbank_IDDB00291
  • ACS_NO305-03-3
  • Show 3D model
  • LogP (experiment)3.25
  • LogP (predicted, AB/LogP v2.0)3.34
  • pka5.8
  • LogD (pH=7, predicted)1.29
  • Solubility (experiment)12.4 mg/ml
  • LogS (predicted, ACD/Labs)(ph=7)-1.65
  • LogSw (predicted, AB/LogsW2.0)0.81
  • Sw (mg/ml) (predicted, ACD/Labs)0.16
  • No.of HBond Donors1
  • No.of HBond Acceptors3
  • No.of Rotatable Bonds9
  • TPSA40.54
  • StatusFDA approved
  • AdministrationN/A
  • PharmacologyA chemotherapy drug that has been mainly used in the treatment of chronic lymphocytic leukemia.
  • Absorption_value100.0
  • Absorption (description)Rapidly absorbed after oral administration with peak plasma concentrations being attained in 0.5 to 2 h.
  • Caco_2N/A
  • Bioavailability87.0
  • Protein binding99.0
  • Volume of distribution (VD)N/A
  • Blood/Plasma Partitioning ratio (D_blood)N/A
  • MetabollsmHepatic
  • Half life1~2 h
  • ExcretionIt is extensively metabolised; less than 1% of a dose is excreted in the urine unchanged. Phenylacetic acid mustard is a major metabolite.
  • Urinary ExcretionN/A
  • CleranceN/A
  • ToxicityThe most common side effect is bone marrow suppression. Other side effects include: gastrointestinal - nausea, vomiting, diarrhea, oral ulceration; central nervous system - tremors, muscular twitching, confusion, agitation, ataxia, flaccid paresis, hallucinations; dermatologic - urticaria, angioneurotic edema; miscellaneous - pulmonary fibrosis, hepatotoxicity and jaundice, drug fever, peripheral neuropathy, interstitial pneumonia, sterile cystitis, infertility, leukemia, and secondary malignancies.
  • LD50 (rat)Letha dose against male Holtzman rats by intraperitoneal injection of the compound, dissolved in cottonseed oil; 3-6 animals/dose level, LD50=92
  • LD50 (mouse)Lethal dose of the compound in mice upon intraperitoneal administration, LD50=49.54