Quinapril Hydrochloride
FDA-approved product (tablet, oral), marketed as Accupril, Quinapril Hydrochloride.
- Registered studies
- 33
- Lab records
- 0
- Pathogens at ≥40%
- 1 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- Cardiovascular disease
- Diabetes mellitus
- Heart failure
- Hypertension
- Kidney failure
- 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- MRSA35.8% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- E. coli33.7% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- K. pneumoniae15.5% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- M. tuberculosis62.3% 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
33registered studies name this medicine, for any condition. 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 Quinapril Hydrochloride 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.
- FurazolidoneExisting use: Other antiinfectives and antiseptics91.4% AI-predicted activityagainst M. tuberculosisLab records exist49 registered studies
- TriflupromazineExisting use: Psychosis90.6% AI-predicted activityagainst M. tuberculosisNo documented evidence found
- ValdecoxibExisting use: Dysmenorrhea, Osteoarthritis, Rheumatic disease and 1 more88.6% AI-predicted activityagainst M. tuberculosisLab records exist31 registered studies
- CelecoxibExisting use: Ankylosing spondylitis, Cancer, Colorectal neoplasm and 15 more87.6% AI-predicted activityagainst M. tuberculosisLab records exist50+ registered studies
- Dorzolamide HydrochlorideExisting use: Glaucoma, Ocular hypertension, Open-angle glaucoma86.8% AI-predicted activityagainst M. tuberculosisLab records exist50+ registered studies
- MethazolamideExisting use: Glaucoma, Open-angle glaucoma85.6% AI-predicted activityagainst M. tuberculosisLab records exist11 registered studies
- AcetazolamideExisting use: Altitude sickness, Angle-closure glaucoma, Congestive heart failure and 5 more85.2% AI-predicted activityagainst M. tuberculosisLab records exist50+ registered studies
- Trifluoperazine HydrochlorideExisting use: Anxiety disorder, Mental or behavioural disorder, Psychosis and 1 more84.6% AI-predicted activityagainst M. tuberculosis1 registered study
- TriclosanExisting use: Phenol and derivatives, Medicated dressings with antiinfectives84.2% AI-predicted activityagainst M. tuberculosisLab records exist50+ registered studies
- NitrofurazoneExisting use: Eye infection, Leishmaniasis, Trypanosomiasis84.0% AI-predicted activityagainst M. tuberculosis8 registered studies
- BrinzolamideExisting use: Glaucoma, Ocular hypertension, Open-angle glaucoma83.8% AI-predicted activityagainst M. tuberculosisLab records exist50+ registered studies
- ZonisamideExisting use: Epilepsy, Focal-onset seizure, Partial epilepsy and 1 more82.8% AI-predicted activityagainst M. tuberculosisLab records exist50+ registered studies
Registered studies
A registration describes a study; it does not establish a positive result.
Effects of Quinapril 40 mg With Alpha Lipoic Acid or Placebo on Diabetes and Hypertension
NCT00795262 · start 2008-07
Registered record
- Registry ID
- NCT00795262
- Conditions
- Diabetes; Hypertension
- Interventions
- Quinapril (Accupril) plus Alpha Lipoic Acid; accupril, placebo; accupril, alpha lipoic acid
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2008-07
- Completion
- 2009-07
- Enrolment
- 23
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionDiabetes; HypertensionInterventionQuinapril (Accupril) plus Alpha Lipoic Acid; accupril, placebo; accupril, alpha lipoic acidPhaseNot applicableRegistry statusCompletedA Comparison of Indapamide SR 1.5 mg With HCTZ 25 mg, in Combination With an ACE-inhibitor, in Patients With Mild to Moderate AHT and Type 2 DM
NCT00980187 · start 2008-03
Registered record
- Registry ID
- NCT00980187
- Conditions
- Hypertension; Type 2 Diabetes Mellitus
- Interventions
- Hydrochlorothiazide; Indapamide
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2008-03
- Completion
- 2010-08
- Enrolment
- 56
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHypertension; Type 2 Diabetes MellitusInterventionHydrochlorothiazide; IndapamidePhasePhase 4Registry statusCompletedBioequivalence Study of Quinapril Hydrochloride 20 mg and Hydrochlorothiazide 25 mg Tablets Under Fasting Conditions
NCT00872781 · start 2007-10
Registered record
- Registry ID
- NCT00872781
- Conditions
- Healthy
- Interventions
- fixed dose combination of Quinapril HCl 20 mg and Hydrochlorothiazide 25 mg tablets
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2007-10
- Completion
- 2007-12
- Enrolment
- 64
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHealthyInterventionfixed dose combination of Quinapril HCl 20 mg and Hydrochlorothiazide 25 mg tabletsPhaseNot applicableRegistry statusCompletedHigh-Dose Quinapril Versus Low-Dose Quinapril Plus Amlodipine in the Treatment of High-Risk Hypertensive Patients
NCT00313547 · start 2006-04
Registered record
- Registry ID
- NCT00313547
- Conditions
- Hypertension
- Interventions
- Quinapril 40 mg; Quinapril 10 mg and amlodipine 5 mg
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Terminated
- Start
- 2006-04
- Completion
- 2008-03
- Enrolment
- 40
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHypertensionInterventionQuinapril 40 mg; Quinapril 10 mg and amlodipine 5 mgPhasePhase 4Registry statusTerminatedBioequivalence Study of Quinapril Hydrochloride 20 mg and Hydrochlorothiazide 25 mg Tablets Under Fed Conditions
NCT00872235 · start 2005-06
Registered record
- Registry ID
- NCT00872235
- Conditions
- Healthy
- Interventions
- fixed-dose combination of quinapril 20 mg and hydrochlorothiazide 25 mg tablets
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2005-06
- Completion
- 2005-11
- Enrolment
- 40
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHealthyInterventionfixed-dose combination of quinapril 20 mg and hydrochlorothiazide 25 mg tabletsPhaseNot applicableRegistry statusCompletedHigh Dose Candesartan Versus Quinapril for Restenosis Prophylaxis After Stent Angioplasty
NCT00154050 · start 2004-05
Registered record
- Registry ID
- NCT00154050
- Conditions
- Arterial Occlusive Diseases
- Interventions
- candesartan (drug) or quinapril (drug)
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2004-05
- Completion
- 2006-07
- Enrolment
- 22
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionArterial Occlusive DiseasesInterventioncandesartan (drug) or quinapril (drug)PhaseNot applicableRegistry statusCompletedNon-Comparative Study To Evaluate Changes In FMD After Quinapril Therapy In Hypertensive Women
NCT00147524 · start 2003-10
Registered record
- Registry ID
- NCT00147524
- Conditions
- Menopause; Hypertension
- Interventions
- quinapril; Laser Doppler imaging
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2003-10
- Completion
- 2005-05
- Enrolment
- 70
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMenopause; HypertensionInterventionquinapril; Laser Doppler imagingPhasePhase 4Registry statusCompletedRenin-Guided Therapeutics in the Management of Untreated, Uncontrolled, or Complicated Hypertension
NCT00684489 · start 2003-09
Registered record
- Registry ID
- NCT00684489
- Conditions
- Hypertension
- Interventions
- clinical hypertension specialist-no specific med. Any anti-hypertension meds.; renin guided therapeutics-no specific med. Any anti-hypertensive med.
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2003-09
- Completion
- 2005-09
- Enrolment
- 52
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHypertensionInterventionclinical hypertension specialist-no specific med. Any anti-hypertension meds.; renin guided therapeutics-no specific med. Any anti-hypertensive med.PhaseNot applicableRegistry statusCompletedFood Study of Quinapril HCl and Hydrochlorothiazide Tablets 20 mg/25 mg to Accuretic™ Tablets 20 mg/25 mg
NCT00648011 · start 2003-08
Registered record
- Registry ID
- NCT00648011
- Conditions
- Healthy
- Interventions
- Quinapril HCl and Hydrochlorothiazide Tablets 20 mg/25 mg; Accuretic™ Tablets 20 mg/25 mg
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2003-08
- Completion
- 2003-09
- Enrolment
- 44
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHealthyInterventionQuinapril HCl and Hydrochlorothiazide Tablets 20 mg/25 mg; Accuretic™ Tablets 20 mg/25 mgPhasePhase 1Registry statusCompletedFasting Study of Quinapril HCl and Hydrochlorothiazide Tablets 20 mg/25 mg to Accuretic™ Tablets 20 mg/25 mg
NCT00649441 · start 2003-08
Registered record
- Registry ID
- NCT00649441
- Conditions
- Healthy
- Interventions
- Quinapril HCl and Hydrochlorothiazide Tablets 20 mg/25 mg; Accuretic™ Tablets 20 mg/25 mg
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2003-08
- Completion
- 2003-09
- Enrolment
- 60
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHealthyInterventionQuinapril HCl and Hydrochlorothiazide Tablets 20 mg/25 mg; Accuretic™ Tablets 20 mg/25 mgPhasePhase 1Registry statusCompletedAmlodipine Diabetic Hypertension Efficacy Response Trial
NCT00159692 · start 2003-03
Registered record
- Registry ID
- NCT00159692
- Conditions
- Hypertension
- Interventions
- Amlodipine
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2003-03
- Completion
- 2005-08
- Enrolment
- 739
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHypertensionInterventionAmlodipinePhasePhase 4Registry statusCompletedFasting Study of Quinapril Hydrochloride Tablets 40 mg and Accupril® Tablets 40 mg
NCT00649103 · start 2002-12
Registered record
- Registry ID
- NCT00649103
- Conditions
- Healthy
- Interventions
- Quinapril Hydrochloride Tablets 40 mg; Accupril® Tablets 40 mg
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2002-12
- Completion
- 2003-01
- Enrolment
- 60
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHealthyInterventionQuinapril Hydrochloride Tablets 40 mg; Accupril® Tablets 40 mgPhasePhase 1Registry statusCompletedFood Study of Quinapril Hydrochloride Tablets 40 mg and Accupril® Tablets 40 mg
NCT00649649 · start 2002-12
Registered record
- Registry ID
- NCT00649649
- Conditions
- Healthy
- Interventions
- Quinapril Hydrochloride Tablets 40 mg; Accupril® Tablets 40 mg
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2002-12
- Completion
- 2003-01
- Enrolment
- 24
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHealthyInterventionQuinapril Hydrochloride Tablets 40 mg; Accupril® Tablets 40 mgPhasePhase 1Registry statusCompletedA Study to Evaluate the Efficacy and Safety of Quinapril or Quinapril Plus Hydrochlorothiazide in Patients With Mild to Moderate Hypertension
NCT00651287 · start 2002-12
Registered record
- Registry ID
- NCT00651287
- Conditions
- Hypertension
- Interventions
- quinapril 20 mg; quinapril 20 mg plus hydrochlorothiazide 12.5 mg; quinapril 40 mg
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2002-12
- Completion
- 2004-06
- Enrolment
- 200
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHypertensionInterventionquinapril 20 mg; quinapril 20 mg plus hydrochlorothiazide 12.5 mg; quinapril 40 mgPhasePhase 4Registry statusCompletedQWISE - Study of Quinapril in Women With Chest Pain, Coronary Flow Reserve Limitations and Evidence of Myocardial Ischemia
NCT00150826 · start 2000-05
Registered record
- Registry ID
- NCT00150826
- Conditions
- Ischemic Heart Disease
- Interventions
- Quinapril; Placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2000-05
- Completion
- 2004-12
- Enrolment
- 78
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionIschemic Heart DiseaseInterventionQuinapril; PlaceboPhasePhase 4Registry statusCompleted