Pyrimethamine
FDA-approved product (tablet, oral), marketed as Daraprim, Pyrimethamine.
- Registered studies
- 50+
- Lab records
- 9
- Pathogens at ≥40%
- 3 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- Malaria
- Toxoplasmosis
Indications ChEMBL records as approved, from FDA and DailyMed labels. Label ↗
- WHO therapeutic group
- Diaminopyrimidines
- FDA pharmacologic class
- Dihydrofolate Reductase Inhibitor Antimalarial FDA label ↗
- Anti-infective classification
- Classified as another kind of anti-infective (for example an antifungal, antiviral or antiparasitic medicine).WHO ATC P01BD01; WHO ATC P01BD51; FDA class Dihydrofolate Reductase Inhibitor Antimalarial
Repurposing investigation
This medicine is being investigated here for AI-predicted antimicrobial activity against MRSA, E. coli and M. tuberculosis. It was surfaced computationally for further investigation; it is not an established treatment for these infections.
AI-predicted activity
AI prediction · nothing measured- MRSA49.0% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates.
- E. coli64.6% AI-predicted activityAt or above the ≥40% mark this site uses to surface candidates. This medicine was in the model's training data, so this is recall, not a new prediction.
- K. pneumoniae11.3% AI-predicted activityBelow the ≥40% mark this site uses to surface candidates.
- M. tuberculosis54.6% 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
- E. coli: measured active in 9 of 9 lab records
Show the 9 laboratory records, with sources
Loading records…
“Active” means the measured value reached this project’s laboratory cutoff (10 µM or stronger). A laboratory result does not show an effect in patients.
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 Pyrimethamine 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.
Folic Acid Supplementation in Gambian Primigravidae
NCT00120822 · start 2002-07
Registered record
- Registry ID
- NCT00120822
- Conditions
- Malaria
- Interventions
- Folic acid
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2002-07
- Completion
- 2004-01
- Enrolment
- 1,000
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMalariaInterventionFolic acidPhasePhase 3Registry statusCompletedEffect of Antimalarial Treatment on Gametocyte Carriage in Asymptomatic P. Falciparum
NCT00289250 · start 2001-05
Registered record
- Registry ID
- NCT00289250
- Conditions
- Asymptomatic P.Falciparum Malaria
- Interventions
- Sulfadoxine-pyrimethamine; Sulfadoxine-pyrimethamine plus artesunate
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Completed
- Start
- 2001-05
- Completion
- 2001-12
- Enrolment
- 360
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAsymptomatic P.Falciparum MalariaInterventionSulfadoxine-pyrimethamine; Sulfadoxine-pyrimethamine plus artesunatePhasePhase 3Registry statusCompletedPyrimethamine and Sulfadoxine for Treatment of Autoimmune Lymphoproliferative Syndrome
NCT00013689 · start 2001-03
Registered record
- Registry ID
- NCT00013689
- Conditions
- Autoimmune Disease; Lymphoproliferative Disorder
- Interventions
- Fansidar (pyrimethamine and sulfadoxine)
- Study type
- INTERVENTIONAL
- Phase
- Phase 1
- Registry status
- Completed
- Start
- 2001-03
- Completion
- 2003-03
- Enrolment
- 8
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAutoimmune Disease; Lymphoproliferative DisorderInterventionFansidar (pyrimethamine and sulfadoxine)PhasePhase 1Registry statusCompletedTherapeutic Efficacy Study of Pyrimethamine/Sulfdoxine (Fansidar®) for the Treatment of Uncomplicated Falciparum Malaria in the Peruvian Amazon
NCT00951106 · start 1998-01
Registered record
- Registry ID
- NCT00951106
- Conditions
- Malaria, Vivax; Malaria, Falciparum
- Interventions
- Pyrimethamine/sulfdoxine (Fansidar)
- Study type
- INTERVENTIONAL
- Phase
- Not applicable
- Registry status
- Completed
- Start
- 1998-01
- Completion
- 2009-08
- Enrolment
- Not recorded
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionMalaria, Vivax; Malaria, FalciparumInterventionPyrimethamine/sulfdoxine (Fansidar)PhaseNot applicableRegistry statusCompletedSP Resistance and Falciparum Malaria Transmission
NCT00299247
Registered record
- Registry ID
- NCT00299247
- Conditions
- Plasmodium Falciparum Malaria
- Interventions
- sulfadoxine/pyrimethamine
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Registry status
- Withdrawn
- Start
- Not recorded
- Completion
- 2006-12
- Enrolment
- 0
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionPlasmodium Falciparum MalariaInterventionsulfadoxine/pyrimethaminePhasePhase 3Registry statusWithdrawn