Cefadroxil

drug
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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

FieldValue
ChEMBL IDCHEMBL1644
NameCefadroxil
TypeSmall molecule
Max phase4
FDA approvedyes
PubChem CID47965
ChEBICHEBI:3479
ATCJ01DB05
Molecular formulaC16H17N3O5S
Molecular weight363.4
InChIKeyBOEGTKLJZSQCCD-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):

TargetpChemblTypeValueUnitActivity ID
SLC15A25.6Ki2500nMCHEMBL_ACT_11002757
SLC15A25.55Ki2800nMCHEMBL_ACT_11002765
Q634245.52Ki3000nMCHEMBL_ACT_11003103
Q634245.52Ki3000nMCHEMBL_ACT_11003104
SLC15A25.52Ki3000nMCHEMBL_ACT_6307771
SLC15A25.52Ki3020nMCHEMBL_ACT_6307845
SLC22A65.21Ki6140nMCHEMBL_ACT_11003210
SLC22A85.06Ki8620nMCHEMBL_ACT_11003289
SLC22A85.06Ki8620nMCHEMBL_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).

IndicationTrial phaseMONDOEFO
bacterial infectious disease4MONDO:0005113EFO:0000771
pharyngitis4MONDO:0002258MONDO:0002258
pulmonary tuberculosis2MONDO:0006052EFO: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

PhaseTrials
PHASE42
PHASE32
PHASE22
PHASE12
Not specified1

Top trials by phase / activity

NCTPhaseStatusTitle
NCT04297592PHASE4ENROLLING_BY_INVITATIONAntibiotic Prophylaxis in High-Risk Arthroplasty Patients
NCT05977868PHASE4TERMINATEDComparing Oral Versus Parenteral Antimicrobial Therapy
NCT02814916PHASE3COMPLETEDDalbavancin 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
NCT04723940PHASE3UNKNOWNOr v IV Antibiotics for Infection
NCT06406114PHASE2RECRUITINGOptimizing the Diagnostic Approach to Cephalosporin Allergy Testing
NCT02381470PHASE2COMPLETEDTrial 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
NCT02479867PHASE1COMPLETEDA Bioequivalence Study of Cefadroxil From Duricef 1 gm F.C.T (GSK) and Biodroxil 1 gm F.C.T (Novartis Pharma)
NCT03802552PHASE1COMPLETEDCefadroxil and Cephalexin Drug Levels and Dosing in Pediatric Musculoskeletal Infections
NCT00405158Not specifiedCOMPLETEDStudy 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.

No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).