Menadione
FDA-approved product (tablet, oral), marketed as Menadione.
- Registered studies
- 50+
- Lab records
- 0
- Pathogens at ≥40%
- 1 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- Hemorrhage
Indications ChEMBL records as approved, from FDA and DailyMed labels.
- WHO therapeutic group
- Vitamin k
- 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- MRSA3.0% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- E. coli14.6% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- K. pneumoniae4.0% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- M. tuberculosis59.8% 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 measuredAutoDock 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 Menadione 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.
- DactinomycinExisting use: Kidney Wilms tumor, Neoplasm95.6% AI-predicted activityagainst MRSALab records exist50+ registered studies
- TaurursodiolExisting use: Bile acids and derivatives79.6% AI-predicted activityagainst MRSA43 registered studies
- LinaclotideExisting use: Constipation, Constipation disorder, Irritable bowel syndrome74.5% AI-predicted activityagainst MRSA50+ registered studies
- PlecanatideExisting use: Constipation74.4% AI-predicted activityagainst MRSA15 registered studies
- OxytocinExisting use: Hemorrhage, Uterine Inertia74.2% AI-predicted activityagainst MRSA50+ registered studies
- PosaconazoleExisting use: Aspergillosis, Candidiasis, Coccidioidomycosis and 2 more72.2% AI-predicted activityagainst MRSA50+ registered studies
- SotorasibExisting use: Neoplasm, Non-small cell lung carcinoma70.6% AI-predicted activityagainst MRSA50+ registered studies
- TemsirolimusExisting use: Cancer, Clear cell renal carcinoma, Mantle cell lymphoma and 2 more70.1% AI-predicted activityagainst MRSA50+ registered studies
- Quizartinib DihydrochlorideExisting use: Acute myeloid leukemia, Myeloid leukemia70.0% AI-predicted activityagainst MRSA4 registered studies
- Irinotecan HydrochlorideExisting use: Adenocarcinoma, Cancer, Carcinoma and 4 more70.0% AI-predicted activityagainst MRSA50+ registered studies
- Deoxycholic AcidExisting use: Other dermatologicals69.3% AI-predicted activityagainst MRSA50+ registered studies
- ChenodiolExisting use: Cerebrotendinous xanthomatosis, Inborn errors of metabolism69.2% AI-predicted activityagainst MRSA30 registered studies
Registered studies
A registration describes a study; it does not establish a positive result.
DULCIS (D-dimer and ULtrasonography in Combination Italian Study)
NCT00954395 · start 2008-09
Registered record
- Registry ID
- NCT00954395
- Conditions
- Venous Thromboembolism
- Interventions
- D-dimer
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Completed
- Start
- 2008-09
- Completion
- 2012-06
- Enrolment
- 1,100
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionVenous ThromboembolismInterventionD-dimerPhaseNot recordedRegistry statusCompletedThe Effect of Vitamin K Supplementation on Bone Health in Adult Crohn's Disease Patients
NCT01235325 · start 2008-07
Registered record
- Registry ID
- NCT01235325
- Conditions
- Supplementation; Bone Health; Crohn's Disease
- Interventions
- phylloquinone (vitamin K1); placebo
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2008-07
- Completion
- 2010-11
- Enrolment
- 70
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionSupplementation; Bone Health; Crohn's DiseaseInterventionphylloquinone (vitamin K1); placeboPhasePhase 4Registry statusCompletedPredictive Value of Coronary Heart Disease (CHD) Biomarkers for CHD Death
NCT01864122 · start 2007-01
Registered record
- Registry ID
- NCT01864122
- Conditions
- Cardiovascular Disease
- Interventions
- Not recorded
- Study type
- OBSERVATIONAL
- Phase
- Not recorded
- Registry status
- Completed
- Start
- 2007-01
- Completion
- 2010-10
- Enrolment
- 2,448
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionCardiovascular DiseaseInterventionNot recordedPhaseNot recordedRegistry statusCompletedChanges in Oral Vitamin K Intake for Optimization of Chronic Oral Anticoagulation: A Randomized Trial
NCT00355290 · start 2006-08
Registered record
- Registry ID
- NCT00355290
- Conditions
- Blood Coagulation Disorders
- Interventions
- Changes on Oral Vitamin K Intake
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 2006-08
- Completion
- 2007-12
- Enrolment
- 114
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionBlood Coagulation DisordersInterventionChanges on Oral Vitamin K IntakePhaseNot applicableRegistry statusCompletedEffect of Vitamin K on Age-Related Bone Loss and Vascular Calcification
NCT00183001 · start 2001-10
Registered record
- Registry ID
- NCT00183001
- Conditions
- Osteoporosis; Vascular Calcification; Inflammation
- Interventions
- Vitamin K
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2001-10
- Completion
- 2006-10
- Enrolment
- 452
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionOsteoporosis; Vascular Calcification; InflammationInterventionVitamin KPhasePhase 3Registry statusCompleted