• Molecular NameCaptopril
  • SynonymCaptoprilum [INN-Latin]; Captopryl; L-Captopril
  • Weight217.289
  • Drugbank_IDDB01197
  • ACS_NO62571-86-2
  • Show 3D model
  • LogP (experiment)0.546
  • LogP (predicted, AB/LogP v2.0)0.67
  • pka3.7, 9.8
  • LogD (pH=7, predicted)-2.92
  • Solubility (experiment)Soluble
  • LogS (predicted, ACD/Labs)(ph=7)0.66
  • LogSw (predicted, AB/LogsW2.0)35.73
  • Sw (mg/ml) (predicted, ACD/Labs)12.42
  • No.of HBond Donors1
  • No.of HBond Acceptors4
  • No.of Rotatable Bonds3
  • TPSA96.41
  • StatusFDA approved
  • AdministrationN/A
  • PharmacologyAn angiotensin-converting enzyme inhibitor (ACE inhibitor) used for the treatment of hypertension and some types of congestive heart failure.
  • Absorption_value84.0
  • Absorption (description)Readily absorbed after oral administration; about 60 to 75% of the dose is absorbed and peak plasma concentrations are achieved within about an hour.
  • Caco_2N/A
  • Bioavailability62.0
  • Protein binding30.0
  • Volume of distribution (VD)0.7 L/kg
  • Blood/Plasma Partitioning ratio (D_blood)N/A
  • Metabollsmhepatic
  • Half life1.9 h
  • Excretion40 to 50% of an oral dose is excreted in the urine as unchanged drug, about 3% as captopril disulfide and about 30% as polar metabolites. Excretion in the urine is rapid, about half the dose being excreted within the first 4 h. An S-methyl metabolite has been identified in plasma and urine. Captopril is removed by haemodialysis.
  • Urinary ExcretionN/A
  • CleranceBlood clearance, about 13 mL/min/kg.
  • ToxicitySymptoms of overdose include coma, lethargy, low blood pressure, sluggishness, and stomach and intestinal irritation and hyperactivity.
  • LD50 (rat)N/A
  • LD50 (mouse)N/A