• Molecular NameEnalapril
  • SynonymEnalapril Maleate; Enalaprila [INN-Spanish]; Enalaprilat; Enalaprilum [INN-Latin]
  • Weight348.399
  • Drugbank_IDDB00584
  • ACS_NO75847-73-3
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  • LogP (experiment)N/A
  • LogP (predicted, AB/LogP v2.0)-1.25
  • pka2.97 and 5.35
  • LogD (pH=7, predicted)-2.3
  • Solubility (experiment)25 mg/mL
  • LogS (predicted, ACD/Labs)(ph=7)0.46
  • LogSw (predicted, AB/LogsW2.0)25.37
  • Sw (mg/ml) (predicted, ACD/Labs)19.96
  • No.of HBond Donors3
  • No.of HBond Acceptors7
  • No.of Rotatable Bonds8
  • TPSA106.94
  • StatusFDA approved
  • AdministrationI.V. and P.O.
  • PharmacologyAn angiotensin converting enzyme (ACE) inhibitor used in the treatment of hypertension and some types of chronic heart failure.
  • Absorption_value63.0
  • Absorption (description)After oral administration, 60% of a dose is absorbed
  • Caco_2-5.64
  • Bioavailability41.0
  • Protein binding55.0
  • Volume of distribution (VD)1.7 L/kg
  • Blood/Plasma Partitioning ratio (D_blood)N/A
  • MetabollsmRapidly and extensively hydrolysed in the liver to enalaprilat. Peak plasma concentrations of enalaprilat are achieved 3 to 4 h after oral dose.
  • Half life11 h
  • ExcretionEnalapril is excreted in urine as the metabolite, enalaprilat, and the rest in faeces as the unchanged drug. After a single oral dose of 20 mg enalapril, enalapril and enalaprilat can be detected in breast milk with a concentration of 1 to 2.3 μg/L for the latter. Enalaprilat is removed by haemodialysis and peritoneal dialysis.
  • Urinary Excretion88
  • Clerance4.9 ml/min/kg
  • ToxicityTreatment with enalapril can result in renal failure, with the possibility of death. Severe hypotension is the main toxic effect and loss of hearing has also been reported by some.
  • LD50 (rat)N/A
  • LD50 (mouse)N/A