Cefdinir
FDA-approved product (capsule, oral), marketed as Cefdinir, Omnicef.
- Registered studies
- 32
- Lab records
- 8
- Pathogens at ≥40%
- 4 of 4
Chemical structure
Existing / approved use
Documented · FDA, WHO, ChEMBLApproved for
- Bacterial disease
- Chronic bronchitis
- Infection
- Infectious otitis media
- Otitis media
- Pharyngitis
- Pneumonia
- Recurrent tonsillitis
Indications ChEMBL records as approved, from FDA and DailyMed labels. Label ↗
- WHO therapeutic group
- Third-generation cephalosporins
- FDA pharmacologic class
- Cephalosporin Antibacterial FDA label ↗
- Anti-infective classification
- Classified as an existing antimicrobial.WHO ATC J01DD15; FDA class Cephalosporin Antibacterial
Repurposing investigation
Cefdinir is already an antimicrobial, so it is not counted among the repurposing candidates. Its AI-predicted activity is shown below for reference.
AI-predicted activity
AI prediction · nothing measured- MRSA99.0% 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.
- E. coli99.4% 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. pneumoniae98.6% 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.
- M. tuberculosis47.6% 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
32registered studies name this medicine, for any condition. See them below.
Experimental
- MRSA: measured active in 2 of 2 lab records
- E. coli: measured active in 4 of 4 lab records
- K. pneumoniae: measured active in 2 of 2 lab records
Show the 8 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 Cefdinir 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.
- Lumateperone TosylateExisting use: Psychosis, Schizophrenia65.8% AI-predicted activityagainst M. tuberculosis6 registered studies
- Moexipril HydrochlorideExisting use: Cardiovascular disease, Hypertension65.8% AI-predicted activityagainst M. tuberculosis12 registered studies
- VismodegibExisting use: Basal cell carcinoma, Cancer, Neoplasm and 1 more65.8% AI-predicted activityagainst M. tuberculosis50+ registered studies
- DarunavirExisting use: HIV infection, HIV-1 infection, Immunodeficiency disease and 2 more65.6% AI-predicted activityagainst M. tuberculosis50+ registered studies
- Lenacapavir SodiumExisting use: HIV infection, HIV-1 infection, Viral disease65.6% AI-predicted activityagainst M. tuberculosisNo documented evidence found
- LisinoprilExisting use: Cardiovascular disease, Congestive heart failure, Diabetes mellitus and 4 more65.6% AI-predicted activityagainst M. tuberculosis50+ registered studies
- Umbralisib TosylateExisting use: Follicular lymphoma, Marginal zone B-cell lymphoma, Neoplasm65.6% AI-predicted activityagainst M. tuberculosisNo documented evidence found
- BrigatinibExisting use: Neoplasm, Non-small cell lung carcinoma65.4% AI-predicted activityagainst M. tuberculosis48 registered studies
- GlyburideExisting use: Diabetes mellitus, Type 2 diabetes mellitus65.4% AI-predicted activityagainst M. tuberculosis50+ registered studies
- ThiothixeneExisting use: Psychosis, Schizophrenia65.4% AI-predicted activityagainst M. tuberculosis5 registered studies
- GefitinibExisting use: Cancer, Neoplasm, Non-small cell lung carcinoma65.4% AI-predicted activityagainst M. tuberculosis50+ registered studies
- PimozideExisting use: Psychosis, Tics, Tourette syndrome65.2% AI-predicted activityagainst M. tuberculosis15 registered studies
Registered studies
A registration describes a study; it does not establish a positive result.
A Comparative, Single-Center, Pediatric Taste Test Study of Omnicef Versus Amoxicillin Antibiotic Suspension Medications
NCT00645125 · start 2003-01
Registered record
- Registry ID
- NCT00645125
- Conditions
- Healthy
- Interventions
- cefdinir (Omnicef); amoxicillin
- Study type
- INTERVENTIONAL
- Phase
- Phase 4
- Registry status
- Completed
- Start
- 2003-01
- Completion
- Not recorded
- Enrolment
- 154
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionHealthyInterventioncefdinir (Omnicef); amoxicillinPhasePhase 4Registry statusCompletedSafety and Efficacy Study of Cefdinir Oral Suspension, in Pediatric Subjects to Treat Acute Otitis Media
NCT00645203 · start 2002-07
Registered record
- Registry ID
- NCT00645203
- Conditions
- Acute Otitis Media
- Interventions
- cefdinir
- Study type
- INTERVENTIONAL
- Phase
- Phase 2 / Phase 3
- Registry status
- Completed
- Start
- 2002-07
- Completion
- Not recorded
- Enrolment
- 447
As stored from ClinicalTrials.gov. Registration describes a study; it does not mean the study worked.
ConditionAcute Otitis MediaInterventioncefdinirPhasePhase 2 / Phase 3Registry statusCompleted