• Molecular NameDosulepin
  • Synonymdothiepin
  • Weight295.45
  • Drugbank_IDN/A
  • ACS_NO113-53-1
  • Show 3D model
  • LogP (experiment)4.52
  • LogP (predicted, AB/LogP v2.0)4.8
  • pka9.25
  • LogD (pH=7, predicted)3.02
  • Solubility (experiment)N/A
  • LogS (predicted, ACD/Labs)(ph=7)-1.99
  • LogSw (predicted, AB/LogsW2.0)0.01
  • Sw (mg/ml) (predicted, ACD/Labs)0.03
  • No.of HBond Donors0
  • No.of HBond Acceptors1
  • No.of Rotatable Bonds3
  • TPSA28.54
  • StatusN/A
  • AdministrationN/A
  • PharmacologyAn antidepressant of the tricyclic family.
  • Absorption_value95.0
  • Absorption (description)Well absorbed after oral administration.
  • Caco_2N/A
  • Bioavailability30.0
  • Protein binding84.0
  • Volume of distribution (VD)N/A
  • Blood/Plasma Partitioning ratio (D_blood)Plasma:whole blood ratio, about 1.4.
  • MetabollsmThe main metabolic reactions are demethylation to desmethyldosulepin (northiaden) and oxidation to dosulepin sulfoxide.
  • Half life22 h, monodesmethyldosulepin 33 h, dosulepin sulfoxide 20 h
  • ExcretionAbout 50 to 60% of a dose is excreted in the urine in 24 h, mainly as metabolites, and 15 to 40% of a dose is eliminated in the faeces in the same period. Enterohepatic circulation has been reported. Small amounts may be excreted in breast milk
  • Urinary ExcretionN/A
  • CleranceN/A
  • ToxicityFatalities have been associated with blood concentrations of 1 to 5 to 19 mg/L.
  • LD50 (rat)N/A
  • LD50 (mouse)N/A