Cefadroxil
drugOn this page
Also known as Anhydrous cefadroxilBaxanBL-S578Cefadroxil (as monohydrate)Cefadroxil anhydrousCefadroxil hydrateCefadroxil monohydrateCefadroxil/cefadroxil hemihydrateCefadroxiloCefadropsCefatabsDuracefDuricefNSC-756664UltracefCephadroxilSID93576712SID144204202[3H]-Cefadroxil
Summary
Cefadroxil (CHEMBL1644) is an approved small-molecule antibacterial drug (ATC J01DB05); indicated across 4 conditions including bacterial infectious disease and pharyngitis.
At a glance
- Status: Approved (max clinical phase 4)
- Modality: Small molecule
- ATC class: J01DB05
- Indications: 4 conditions
- Clinical trials: 9
- Chemistry: 363.4 Da · C16H17N3O5S
Identifiers
Drug identity and classification
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL1644 |
| Name | Cefadroxil |
| Type | Small molecule |
| Max phase | 4 |
| FDA approved | yes |
| PubChem CID | 47965 |
| ChEBI | CHEBI:3479 |
| ATC | J01DB05 |
| Molecular formula | C16H17N3O5S |
| Molecular weight | 363.4 |
| InChIKey | BOEGTKLJZSQCCD-UEKVPHQBSA-N |
SMILES: CC1=C(N2[C@@H]([C@@H](C2=O)NC(=O)[C@@H](C3=CC=C(C=C3)O)N)SC1)C(=O)O
IUPAC name: (6R,7R)-7-[[(2R)-2-amino-2-(4-hydroxyphenyl)acetyl]amino]-3-methyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
ChEBI definition: A cephalosporin bearing methyl and (2R)-2-amino-2-(4-hydroxyphenyl)acetamido groups at positions 3 and 7, respectively, of the cephem skeleton.
Pharmacological roles (ChEBI): antibacterial drug.
Also known as: Anhydrous cefadroxil, Baxan, BL-S578, Cefadroxil, Cefadroxil (as monohydrate), Cefadroxil anhydrous, Cefadroxil hydrate, Cefadroxil monohydrate, Cefadroxil/cefadroxil hemihydrate, Cefadroxilo, Cefadrops, Cefatabs
Patent coverage: 1,817 distinct patent families (6,102 SureChEMBL compound mentions), from 1 matched compound structure(s). Mentions count patents naming the compound (not distinct inventions), so promiscuous / reference molecules inflate the mention figure — families are the dedup metric.
Targets
Targets
Broader ChEMBL bioactivity targets: 6 (assay-derived). Sample: Solute carrier family 22 member 6, Organic anion transporter 3, Solute carrier family 15 member 2, Estrogen receptor, Glutamate receptor ionotropic, NMDA 1, Solute carrier family 15 member 2.
Bioactivity
ChEMBL activities: 9 potent at pChembl ≥ 5 of 12 total. Top 30 by potency (10 = 0.1 nM, 6 = 1 µM):
| Target | pChembl | Type | Value | Unit | Activity ID |
|---|---|---|---|---|---|
| SLC15A2 | 5.6 | Ki | 2500 | nM | CHEMBL_ACT_11002757 |
| SLC15A2 | 5.55 | Ki | 2800 | nM | CHEMBL_ACT_11002765 |
| Q63424 | 5.52 | Ki | 3000 | nM | CHEMBL_ACT_11003103 |
| Q63424 | 5.52 | Ki | 3000 | nM | CHEMBL_ACT_11003104 |
| SLC15A2 | 5.52 | Ki | 3000 | nM | CHEMBL_ACT_6307771 |
| SLC15A2 | 5.52 | Ki | 3020 | nM | CHEMBL_ACT_6307845 |
| SLC22A6 | 5.21 | Ki | 6140 | nM | CHEMBL_ACT_11003210 |
| SLC22A8 | 5.06 | Ki | 8620 | nM | CHEMBL_ACT_11003289 |
| SLC22A8 | 5.06 | Ki | 8620 | nM | CHEMBL_ACT_15445017 |
Target pathways
No target-pathway data for this drug (no mapped target genes).
Indications & clinical
Indications
4 indications (3 at ChEMBL trial phase 4). Phase below is the highest clinical-trial phase recorded for this drug against each disease — not the molecule’s overall approval status (that is in the Summary).
| Indication | Trial phase | MONDO | EFO |
|---|---|---|---|
| bacterial infectious disease | 4 | MONDO:0005113 | EFO:0000771 |
| pharyngitis | 4 | MONDO:0002258 | MONDO:0002258 |
| pulmonary tuberculosis | 2 | MONDO:0006052 | EFO:1000049 |
1 further indication record had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.
Clinical trials
Total trials: 9.
Phase distribution
| Phase | Trials |
|---|---|
| PHASE4 | 2 |
| PHASE3 | 2 |
| PHASE2 | 2 |
| PHASE1 | 2 |
| Not specified | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT04297592 | PHASE4 | ENROLLING_BY_INVITATION | Antibiotic Prophylaxis in High-Risk Arthroplasty Patients |
| NCT05977868 | PHASE4 | TERMINATED | Comparing Oral Versus Parenteral Antimicrobial Therapy |
| NCT02814916 | PHASE3 | COMPLETED | Dalbavancin for the Treatment of Acute Bacterial Skin and Skin Structure Infections in Children, Known or Suspected to be Caused by Susceptible Gram-positive Organisms, Including MRSA |
| NCT04723940 | PHASE3 | UNKNOWN | Or v IV Antibiotics for Infection |
| NCT06406114 | PHASE2 | RECRUITING | Optimizing the Diagnostic Approach to Cephalosporin Allergy Testing |
| NCT02381470 | PHASE2 | COMPLETED | Trial of Faropenem and Cefadroxil (in Combination With Amoxicillin/Clavulanic Acid and Standard TB Drugs) in Patients With Pulmonary Tuberculosis: Measurement of Early Bactericidal Activity and Effects on Novel Biomarkers |
| NCT02479867 | PHASE1 | COMPLETED | A Bioequivalence Study of Cefadroxil From Duricef 1 gm F.C.T (GSK) and Biodroxil 1 gm F.C.T (Novartis Pharma) |
| NCT03802552 | PHASE1 | COMPLETED | Cefadroxil and Cephalexin Drug Levels and Dosing in Pediatric Musculoskeletal Infections |
| NCT00405158 | Not specified | COMPLETED | Study of Acupuncture and Care Interventions for the Treatment of Breast Inflammation During Breastfeeding |
Clinical evidence (CIViC)
No CIViC predictive evidence (expected for non-precision-medicine drugs).
Pharmacology
Pharmacogenomics
No PharmGKB pharmacogenomic data curated for this drug.
Related molecules
Related molecules
No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).
Related Atlas pages
- Diseases: bacterial infectious disease, pharyngitis