Lisinopril
FDA-approved product (tablet, oral), marketed as Lisinopril, Prinivil, Qbrelis 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
- Diabetes mellitus
- Heart failure
- Hypertension
- Myocardial infarction
- Stroke
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- MRSA39.6% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- E. coli29.8% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- K. pneumoniae23.4% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- M. tuberculosis65.6% 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 Lisinopril 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.
- UrsodiolExisting use: Biliary liver cirrhosis, Primary biliary cirrhosis69.2% AI-predicted activityagainst MRSA50+ registered studies
- OlaparibExisting use: Breast cancer, Breast carcinoma, Breast neoplasm and 9 more69.2% AI-predicted activityagainst MRSA50+ registered studies
- Ganirelix AcetateExisting use: Female infertility, Positive regulation of ovulation, Reproductive Techniques, Assisted69.1% AI-predicted activityagainst MRSA50+ registered studies
- DanicopanExisting use: Acquired paroxysmal nocturnal hemoglobinuria, Hemoglobinuria, Paroxysmal, Hemolysis68.7% AI-predicted activityagainst MRSA30 registered studies
- Simeprevir SodiumExisting use: Chronic hepatitis C virus infection68.6% AI-predicted activityagainst MRSANo documented evidence found
- Lanreotide AcetateExisting use: Acromegaly, Carcinoid syndrome68.3% AI-predicted activityagainst MRSA50+ registered studies
- Cholic AcidExisting use: Abnormality of the gastrointestinal tract, Inborn errors of metabolism, Liver disease and 1 more68.0% AI-predicted activityagainst MRSA50+ registered studies
- EptifibatideExisting use: Acute coronary syndrome, Acute myocardial infarction, Intermediate coronary syndrome and 2 more67.8% AI-predicted activityagainst MRSA35 registered studies
- AbarelixExisting use: Neoplasm67.7% AI-predicted activityagainst MRSA5 registered studies
- EverolimusExisting use: Adenoma sebaceum, Anaplastic astrocytoma, Angiomyolipoma and 18 more67.5% AI-predicted activityagainst MRSA50+ registered studies
- Paliperidone PalmitateExisting use: Mental or behavioural disorder, Psychosis, Schizoaffective disorder and 1 more67.3% AI-predicted activityagainst MRSA50+ registered studies
- PaliperidoneExisting use: Mental or behavioural disorder, Psychosis, Schizoaffective disorder and 1 more67.2% AI-predicted activityagainst MRSA50+ registered studies
Registered studies
A registration describes a study; it does not establish a positive result.
Pharmacologic Therapies to Mitigate Radiation- Associated Heart Disease
NCT07685938 · start 2026-08-12
Registered record
- Registry ID
- NCT07685938
- Conditions
- Chest Wall Tumor; Breast Cancer; Lung Cancer; Esophageal Cancer; Mediastinal Cancers; Spine Metastases; Spinal Tumor; Thoracic Cancer; Thoracic Neoplasms
- Interventions
- Atorvastatin and Lisinopril; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Recruiting
- Start
- 2026-08-12
- Completion
- 2029-02
- Enrolment
- 60
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionChest Wall Tumor; Breast Cancer; Lung Cancer; Esophageal Cancer +5 moreInterventionAtorvastatin and Lisinopril; PlaceboPhasePhase 2Registry statusRecruitingThe Effect Of Lisinopril On Polycythemia
NCT07594535 · start 2026-07-01
Registered record
- Registry ID
- NCT07594535
- Conditions
- Polycythemia
- Interventions
- Lisinopril Tablets
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Recruiting
- Start
- 2026-07-01
- Completion
- 2029-07-01
- Enrolment
- 30
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPolycythemiaInterventionLisinopril TabletsPhasePhase 4Registry statusRecruitingThe Assessment of Partial Guideline-Directed Medical Therapy Down Titration in Heart Failure in Remission.
NCT07513883 · start 2026-03-16
Registered record
- Registry ID
- NCT07513883
- Conditions
- Heart Failure
- Interventions
- Down-titration; Continuation of guideline-directed heart failure therapy
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Recruiting
- Start
- 2026-03-16
- Completion
- 2028-12
- Enrolment
- 100
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHeart FailureInterventionDown-titration; Continuation of guideline-directed heart failure therapyPhasePhase 4Registry statusRecruitingImpact of Medically Supervised Performance-Enhancing Substances (PES) on Elite Athletes
NCT07568574 · start 2026-03-12
Registered record
- Registry ID
- NCT07568574
- Conditions
- Safety and Impact of Medically Supervised Performance Enhancing Substance Usage in Healthy Elite Athletes
- Interventions
- Testosterone Enanthate; Testosterone Cypionate; Testosterone Propionate; Sustanon (testosterone); Testosterone Gel; Methenolone Enanthate (Primobolan); Nandrolone Decanoate (Deca-Durabolin); Estradiol Patch; Estradiol Capsule; Progesterone Cream; Progesterone Capsule; Human Growth Hormone (hGH); EPO Darbepoetin (Aranesp); Meldonium; Modafinil; Mixed amphetamine salts (Adderall); Clomiphene; Anastrozole; Levothyroxine; Liothyronine; hCG; hMG; Atorvastatin; Rosuvastatin; Bisoprolol; Nebivolol; Metoprolol; Propranolol; Lisinopril; Enalapril; Furosemide; Chlorothiazide; Cabergoline; Metformin; Basal Insulin Glargine (long-acting); Telmisartan; Losartan
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Enrolling by invitation
- Start
- 2026-03-12
- Completion
- 2033-03-01
- Enrolment
- 60
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSafety and Impact of Medically Supervised Performance Enhancing Substance Usage in Healthy Elite AthletesInterventionTestosterone Enanthate; Testosterone Cypionate; Testosterone Propionate; Sustanon (testosterone) +33 morePhaseNot applicableRegistry statusEnrolling by invitationTreatment of Patients With Diabetic Kidney Disease
NCT06187493 · start 2024-01-01
Registered record
- Registry ID
- NCT06187493
- Conditions
- Diabetic Kidney Disease
- Interventions
- lisinopril, enalapril; dapagliflozin, empagliflozin
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Unknown
- Start
- 2024-01-01
- Completion
- 2025-12-31
- Enrolment
- 70
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionDiabetic Kidney DiseaseInterventionlisinopril, enalapril; dapagliflozin, empagliflozinPhaseNot applicableRegistry statusUnknownSafety and Efficacy of Two Year of RAAS Alone or in Combination With Spironolactone Therapy
NCT03502031 · start 2018-10-01
Registered record
- Registry ID
- NCT03502031
- Conditions
- Renal Insufficiency, Chronic; Diabetic Nephropathy Type 2
- Interventions
- Renin-Angiotensin (RAAS) alone; Renin-Angiotensin (RAAS) blockers in combination with Spironolactone
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Unknown
- Start
- 2018-10-01
- Completion
- 2024-10-01
- Enrolment
- 72
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionRenal Insufficiency, Chronic; Diabetic Nephropathy Type 2InterventionRenin-Angiotensin (RAAS) alone; Renin-Angiotensin (RAAS) blockers in combination with SpironolactonePhasePhase 4Registry statusUnknownWomen's IschemiA TRial to Reduce Events In Non-ObstRuctive CAD
NCT03417388 · start 2018-02-09
Registered record
- Registry ID
- NCT03417388
- Conditions
- Coronary Artery Disease
- Interventions
- High dose potent statin; ACE-I (lisinopril) or ARB (losartan); Aspirin 81 enteric coated tablet daily; Lifestyle Counseling; Quality of Life Questionnaires
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Active not recruiting
- Start
- 2018-02-09
- Completion
- 2026-09-14
- Enrolment
- 2,476
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCoronary Artery DiseaseInterventionHigh dose potent statin; ACE-I (lisinopril) or ARB (losartan); Aspirin 81 enteric coated tablet daily; Lifestyle Counseling +1 morePhasePhase 4Registry statusActive not recruitingComparison of Optimal Hypertension Regimens
NCT02847338 · start 2016-11
Registered record
- Registry ID
- NCT02847338
- Conditions
- Hypertension
- Interventions
- Amlodipine; Lisinopril; Amiloride; Chlortalidone
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2016-11
- Completion
- 2023-10
- Enrolment
- 940
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHypertensionInterventionAmlodipine; Lisinopril; Amiloride; ChlortalidonePhasePhase 4Registry statusCompletedThe Use of Ambulatory Blood Pressure Monitors to Assess Angiotensin Converting Enzyme Inhibitors
NCT02623036 · start 2015-11
Registered record
- Registry ID
- NCT02623036
- Conditions
- Hypertension, Resistant to Conventional Therapy
- Interventions
- Equivalent dose enalapril; Equivalent dose lisinopril
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Unknown
- Start
- 2015-11
- Completion
- 2018-04
- Enrolment
- 20
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHypertension, Resistant to Conventional TherapyInterventionEquivalent dose enalapril; Equivalent dose lisinoprilPhasePhase 1Registry statusUnknownCAndesartan vs LIsinopril Effects on the BRain
NCT01984164 · start 2014-08-20
Registered record
- Registry ID
- NCT01984164
- Conditions
- Hypertension; Mild Cognitive Impairment
- Interventions
- Candesartan; Lisinopril
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Completed
- Start
- 2014-08-20
- Completion
- 2018-12-03
- Enrolment
- 176
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHypertension; Mild Cognitive ImpairmentInterventionCandesartan; LisinoprilPhasePhase 2Registry statusCompletedTreatment of Resistant Hypertension by Prevention of T-Cell Co-Stimulation
NCT02232880 · start 2014-08
Registered record
- Registry ID
- NCT02232880
- Conditions
- Hypertension
- Interventions
- Abatacept; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 2
- Registry status
- Terminated
- Start
- 2014-08
- Completion
- 2015-06
- Enrolment
- 1
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHypertensionInterventionAbatacept; PlaceboPhasePhase 2Registry statusTerminatedSystematic Withdrawal of Neurohumoral Blocker Therapy in Optimally Responding CRT Patients
NCT02200822 · start 2014-07
Registered record
- Registry ID
- NCT02200822
- Conditions
- Heart Failure (HF)
- Interventions
- beta blockers; RAAS blockers
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2014-07
- Completion
- 2019-02
- Enrolment
- 80
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHeart Failure (HF)Interventionbeta blockers; RAAS blockersPhasePhase 4Registry statusCompletedModulation of Heme Oxygenase 1 by Nizatidine and Lisinopril in Healthy Subjects
NCT02232308 · start 2014-07
Registered record
- Registry ID
- NCT02232308
- Conditions
- Gastroparesis
- Interventions
- Nizatidine; Lisinopril; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2014-07
- Completion
- 2014-09
- Enrolment
- 24
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionGastroparesisInterventionNizatidine; Lisinopril; PlaceboPhasePhase 1Registry statusCompletedDose Titration of Lisinopril in Children Aged 1 to 18 Years With Primary or Secondary Hypertension
NCT02184858 · start 2014-06-25
Registered record
- Registry ID
- NCT02184858
- Conditions
- Primary Hypertension; Secondary Hypertension
- Interventions
- lisinopril, ACE-inhibitor
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2014-06-25
- Completion
- 2018-09-17
- Enrolment
- 13
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPrimary Hypertension; Secondary HypertensionInterventionlisinopril, ACE-inhibitorPhasePhase 4Registry statusCompletedA Trial Investigating the Influence of Oral Semaglutide on the Pharmacokinetics of Lisinopril and Warfarin in Healthy Subjects
NCT02070510 · start 2014-02-27
Registered record
- Registry ID
- NCT02070510
- Conditions
- Diabetes; Healthy
- Interventions
- semaglutide; lisinopril; warfarin; placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2014-02-27
- Completion
- 2014-08-20
- Enrolment
- 52
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionDiabetes; HealthyInterventionsemaglutide; lisinopril; warfarin; placeboPhasePhase 1Registry statusCompleted