Enalapril Maleate
FDA-approved product (tablet, oral), marketed as Enalapril Maleate, Epaned, Epaned Kit and 1 more.
- Registered studies
- 50+
- Lab records
- 0
- Pathogens at ≥40%
- 1 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- Cardiovascular disease
- Congestive heart failure
- Heart failure
- Hypertension
- Ventricular Dysfunction, Left
Indications ChEMBL records as approved, from FDA and DailyMed labels. Label ↗
- WHO therapeutic group
- Ace inhibitors, plain
- Anti-infective classification
- Not classified as an anti-infective.
Repurposing investigation
This medicine is being investigated here for AI-predicted antimicrobial activity against M. tuberculosis. It was surfaced computationally for further investigation; it is not an established treatment for this infection.
AI-predicted activity
AI prediction · nothing measured- MRSA33.7% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- E. coli22.0% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- K. pneumoniae14.0% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- M. tuberculosis69.1% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
A model’s estimate of laboratory activity against each pathogen species. It is not clinical effectiveness.
Evidence
Clinical and experimental
Documented evidenceClinical
50+registered studies name this medicine, for any condition. The registry search keeps the first 50, so there may be more. See them below.
Experimental
No evidence found
No laboratory measurement against the four pathogens in the ChEMBL records loaded here.
Docking
Computational · nothing measuredDihydrofolate reductase ↗ (E. coli)
Not yet docked: queued in the docking rundetails
KPC-2 carbapenemase ↗ (K. pneumoniae)
Not yet docked: queued in the docking rundetails
Enoyl-ACP reductase (InhA) ↗ (M. tuberculosis)
Not yet docked: queued in the docking rundetails
Dihydrofolate reductase ↗ (MRSA)
Not yet docked: queued in the docking rundetails
AutoDock Vina, one experimentally solved protein per pathogen. This project’s screening target is -7.0 kcal/mol, its own mark rather than a universal cutoff. A docking score is a structural hypothesis, not proof of binding, and requires experimental validation.
Other medicines to investigate
AI prediction · nothing measuredOther repurposing candidates: approved medicines besides Enalapril Maleate with AI-predicted activity ≥40% against the chosen pathogen, leaving out existing antimicrobials. They are computational candidates for further investigation, not alternatives and not recommendations.
Sorted by AI-predicted activity, high to low. The order is not a ranking of which medicine is better.
- PlecanatideExisting use: Constipation52.2% AI-predicted activityagainst K. pneumoniae15 registered studies
- SotorasibExisting use: Neoplasm, Non-small cell lung carcinoma51.3% AI-predicted activityagainst K. pneumoniae50+ registered studies
- Lanreotide AcetateExisting use: Acromegaly, Carcinoid syndrome50.5% AI-predicted activityagainst K. pneumoniae50+ registered studies
- Terlipressin AcetateExisting use: Hepatorenal syndrome, Kidney failure, Renal insufficiency49.5% AI-predicted activityagainst K. pneumoniae7 registered studies
- LetermovirExisting use: Cytomegalovirus infection, Infection, Viral disease49.0% AI-predicted activityagainst K. pneumoniae50+ registered studies
- Codeine SulfateExisting use: Cough, Drug dependence, Migraine disorder and 2 more48.8% AI-predicted activityagainst K. pneumoniae23 registered studies
- Bromocriptine MesylateExisting use: Acromegaly, Adenoma, Hyperprolactinemia and 4 more48.5% AI-predicted activityagainst K. pneumoniae50+ registered studies
- PimecrolimusExisting use: Atopic eczema, Eczematoid dermatitis48.3% AI-predicted activityagainst K. pneumoniae50+ registered studies
- LypressinExisting use: Vasopressin and analogues48.2% AI-predicted activityagainst K. pneumoniae50+ registered studies
- Degarelix AcetateExisting use: Prostate adenocarcinoma, Prostate cancer, Prostate carcinoma48.2% AI-predicted activityagainst K. pneumoniae50+ registered studies
- OlaparibExisting use: Breast cancer, Breast carcinoma, Breast neoplasm and 9 more48.1% AI-predicted activityagainst K. pneumoniae50+ registered studies
- Dolutegravir SodiumExisting use: HIV infection, HIV-1 infection47.9% AI-predicted activityagainst K. pneumoniae50+ registered studies
Registered studies
A registration describes a study; it does not establish a positive result.
This Study Will Evaluate the Efficacy and Safety of LCZ696 Compared to Enalapril on Morbidity and Mortality of Patients With Chronic Heart Failure
NCT01035255 · start 2009-12
Registered record
- Registry ID
- NCT01035255
- Conditions
- Heart Failure With Reduced Ejection Fraction
- Interventions
- LCZ696 200 mg BID; Enalapril 10 mg BID
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Terminated
- Start
- 2009-12
- Completion
- 2014-05
- Enrolment
- 8,442
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHeart Failure With Reduced Ejection FractionInterventionLCZ696 200 mg BID; Enalapril 10 mg BIDPhasePhase 3Registry statusTerminatedPrognostic Value of the Circadian Pattern of Ambulatory Blood Pressure for Multiple Risk Assessment
NCT00741585 · start 2008-09-01
Registered record
- Registry ID
- NCT00741585
- Conditions
- Essential Hypertension; Cardiovascular Disease; Stroke; Chronic Kidney Disease
- Interventions
- Any antihypertensive medication alone or in combination; Any antihypertensive medication alone or in combination; Ambulatory blood pressure monitoring
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2008-09-01
- Completion
- 2018-06-30
- Enrolment
- 21,983
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionEssential Hypertension; Cardiovascular Disease; Stroke; Chronic Kidney DiseaseInterventionAny antihypertensive medication alone or in combination; Any antihypertensive medication alone or in combination; Ambulatory blood pressure monitoringPhasePhase 4Registry statusCompletedChina Stroke Primary Prevention Trial
NCT00794885 · start 2008-05
Registered record
- Registry ID
- NCT00794885
- Conditions
- Primary Hypertension
- Interventions
- Enalapril/folic acid; Enalapril maleate
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2008-05
- Completion
- 2014-06
- Enrolment
- 20,702
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPrimary HypertensionInterventionEnalapril/folic acid; Enalapril maleatePhasePhase 4Registry statusCompletedCSPPT- Chronic Kidney Diseases Study
NCT01871740 · start 2008-05
Registered record
- Registry ID
- NCT01871740
- Conditions
- Hypertension; Hyperhomocysteinemia
- Interventions
- Enalapril maleate and folic acid tablets; Enalapril maleate
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Withdrawn
- Start
- 2008-05
- Completion
- 2014-08
- Enrolment
- 0
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHypertension; HyperhomocysteinemiaInterventionEnalapril maleate and folic acid tablets; Enalapril maleatePhasePhase 4Registry statusWithdrawnEffect of Sitagliptin and an ACE Inhibitor on Blood Pressure in Metabolic Syndrome
NCT00666848 · start 2008-03
Registered record
- Registry ID
- NCT00666848
- Conditions
- Metabolic Syndrome; Hypertension
- Interventions
- Placebo; Enalapril 5mg; Enalapril 10mg; Sitagliptin
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2008-03
- Completion
- 2010-01
- Enrolment
- 24
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMetabolic Syndrome; HypertensionInterventionPlacebo; Enalapril 5mg; Enalapril 10mg; SitagliptinPhasePhase 4Registry statusCompletedEffect of Turmeric on Diabetic Nephropathy
NCT01015937 · start 2008-03
Registered record
- Registry ID
- NCT01015937
- Conditions
- Diabetic Nephropathy; Proteinuria
- Interventions
- Turmeric extract; Angiotensin-converting enzyme (ACE) inhibitor + Angiotensin-II type 1 receptor (ATI) blocker
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2008-03
- Completion
- 2009-08
- Enrolment
- 50
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionDiabetic Nephropathy; ProteinuriaInterventionTurmeric extract; Angiotensin-converting enzyme (ACE) inhibitor + Angiotensin-II type 1 receptor (ATI) blockerPhaseNot applicableRegistry statusCompletedPrevention of Diabetes and Hypertension
NCT00456963 · start 2007-09
Registered record
- Registry ID
- NCT00456963
- Conditions
- Diabetes Mellitus; Hypertension
- Interventions
- Diet; Moderate exercise; enalapril tablets; placebo tablets; Losartan Tablets
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Terminated
- Start
- 2007-09
- Completion
- 2010-03
- Enrolment
- 3,000
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionDiabetes Mellitus; HypertensionInterventionDiet; Moderate exercise; enalapril tablets; placebo tablets +1 morePhasePhase 4Registry statusTerminatedThe Fabrazyme® and Arbs and ACE Inhibitor Treatment (FAACET) Study
NCT00446862 · start 2007-03
Registered record
- Registry ID
- NCT00446862
- Conditions
- Fabry Disease; Proteinuria
- Interventions
- enalapril and other angiotensin converting enzyme inhibitors; losartan and other angiotensin receptor blockers
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Completed
- Start
- 2007-03
- Completion
- 2012-12
- Enrolment
- 36
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionFabry Disease; ProteinuriaInterventionenalapril and other angiotensin converting enzyme inhibitors; losartan and other angiotensin receptor blockersPhaseNot recordedRegistry statusCompletedIntracerebral Hemorrhage Acutely Decreasing Arterial Pressure Trial
NCT00963976 · start 2007-01
Registered record
- Registry ID
- NCT00963976
- Conditions
- Intracerebral Hemorrhage
- Interventions
- labetalol/hydralazine/enalapril
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2007-01
- Completion
- 2012-02
- Enrolment
- 74
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionIntracerebral HemorrhageInterventionlabetalol/hydralazine/enalaprilPhasePhase 2Registry statusCompletedARCHIPELAGO: Irbesartan in Patients With Acute Coronary Syndrome Without ST Segment Elevation
NCT00296218 · start 2006-02
Registered record
- Registry ID
- NCT00296218
- Conditions
- Myocardial Ischemia; Hypertension
- Interventions
- Irbesartan
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2006-02
- Completion
- Not recorded
- Enrolment
- 440
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMyocardial Ischemia; HypertensionInterventionIrbesartanPhasePhase 3Registry statusCompletedSirolimus Therapy for Poor Prognosis Immunoglobulin A Nephropathy
NCT00396721 · start 2006-01
Registered record
- Registry ID
- NCT00396721
- Conditions
- Glomerulonephritis, IGA; Nephropathy, IGA; IGA Nephropathy
- Interventions
- ACE inhibitor + statin; Sirolimus (study drug)+ACE inhibitor + statin
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2006-01
- Completion
- 2010-02
- Enrolment
- 23
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionGlomerulonephritis, IGA; Nephropathy, IGA; IGA NephropathyInterventionACE inhibitor + statin; Sirolimus (study drug)+ACE inhibitor + statinPhasePhase 2Registry statusCompletedEffect of Enalapril and Losartan Association Therapy on Proteinuria and Inflammatory Biomarkers in Diabetic Nephropathy: a Clinical Trial on Type 2 Diabetes Mellitus
NCT00419835 · start 2005-05
Registered record
- Registry ID
- NCT00419835
- Conditions
- Macroalbuminuric Diabetic Nephropathy
- Interventions
- enalapril; losartan
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2005-05
- Completion
- 2007-09
- Enrolment
- 80
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMacroalbuminuric Diabetic NephropathyInterventionenalapril; losartanPhasePhase 4Registry statusCompletedComparison of the Antihypertensive Efficacy of Valsartan and Enalapril After Missing One Dose
NCT00302705 · start 2005-01
Registered record
- Registry ID
- NCT00302705
- Conditions
- Hypertension
- Interventions
- Valsartan, Enalapril; Ambulatory blood pressure monitoring; Missing one dose
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2005-01
- Completion
- 2007-03
- Enrolment
- 150
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHypertensionInterventionValsartan, Enalapril; Ambulatory blood pressure monitoring; Missing one dosePhasePhase 4Registry statusCompletedMortality Control Program for Economically Productive Age Group in Tribal Area of Melghat.
NCT07436104 · start 2004-01-01
Registered record
- Registry ID
- NCT07436104
- Conditions
- Hypertension (HTN); Diarrhea; Pneumonia; Malaria Fever; COPD; Asthma (Diagnosis); Diarrhea Chronic
- Interventions
- Trained village health workers (VHWs) , provided treatment of HTN, diarrhoea, malaria, pneumonia, asthma and COPD by Amlodipine, ORS, Norfloxacin, Chloroquine, Azithromycin, salbutamol rotacaps; Appropriate referral
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2004-01-01
- Completion
- 2023-08-31
- Enrolment
- 72,564
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHypertension (HTN); Diarrhea; Pneumonia; Malaria Fever +3 moreInterventionTrained village health workers (VHWs) , provided treatment of HTN, diarrhoea, malaria, pneumonia, asthma and COPD by Amlodipine, ORS, Norfloxacin, Chloroquine, Azithromycin, salbutamol rotacaps; Appropriate referralPhasePhase 4Registry statusCompletedAspirin and Enalapril in Microalbuminuric Type 2 Diabetes Mellitus Patients
NCT00427271 · start 2003-03
Registered record
- Registry ID
- NCT00427271
- Conditions
- Diabetes Mellitus; Microalbuminuria
- Interventions
- aspirin
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Unknown
- Start
- 2003-03
- Completion
- 2007-01
- Enrolment
- 20
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionDiabetes Mellitus; MicroalbuminuriaInterventionaspirinPhasePhase 4Registry statusUnknown