Cefpodoxime

drug
On this page

Also known as CefpodoximaEpoximOreloxOrelox paed

Summary

Cefpodoxime (CHEMBL1672) is an approved small-molecule antibacterial drug (ATC J01DD13); indicated across 1 condition including bacterial infectious disease.

At a glance

  • Status: Approved (max clinical phase 4)
  • Modality: Small molecule
  • ATC class: J01DD13
  • Indications: 1 condition
  • Clinical trials: 5
  • Chemistry: 427.5 Da · C15H17N5O6S2

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL1672
NameCefpodoxime
TypeSmall molecule
Max phase4
FDA approvedyes
PubChem CID6335986
ChEBICHEBI:3504
ATCJ01DD13
Molecular formulaC15H17N5O6S2
Molecular weight427.5
InChIKeyWYUSVOMTXWRGEK-HBWVYFAYSA-N

SMILES: COCC1=C(N2[C@@H]([C@@H](C2=O)NC(=O)/C(=N\OC)/C3=CSC(=N3)N)SC1)C(=O)O

IUPAC name: (6R,7R)-7-[[(2Z)-2-(2-amino-1,3-thiazol-4-yl)-2-methoxyiminoacetyl]amino]-3-(methoxymethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid

ChEBI definition: A third-generation cephalosporin antibiotic with methoxymethyl and (2Z)-2-(2-amino-1,3-thiazol-4-yl)-2-(methoxyimino)acetamino substituents at positions 3 and 7, respectively, of the cephem skeleton. Given by mouth as its proxetil ester prodrug, it is used to treat acute otitis media, pharyngitis, and sinusitis.

Pharmacological roles (ChEBI): antibacterial drug.

Also known as: Cefpodoxima, Cefpodoxime, Epoxim, Orelox, Orelox paed, cefpodoxime, CEFPODOXIME

Patent coverage: 4,472 distinct patent families (17,039 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: 2 (assay-derived). Sample: 5-hydroxytryptamine receptor 2C, Nuclear receptor subfamily 1 group I member 2.

Bioactivity

ChEMBL activities: 1 potent at pChembl ≥ 5 of 2 total. Top 30 by potency (10 = 0.1 nM, 6 = 1 µM):

TargetpChemblTypeValueUnitActivity ID
HTR2C6.92AC50120nMCHEMBL_ACT_25131627

Target pathways

No target-pathway data for this drug (no mapped target genes).

Indications & clinical

Indications

1 indication (1 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

Clinical trials

Total trials: 5.

Phase distribution

PhaseTrials
Not specified2
PHASE41
PHASE21
PHASE11

Top trials by phase / activity

NCTPhaseStatusTitle
NCT05977868PHASE4TERMINATEDComparing Oral Versus Parenteral Antimicrobial Therapy
NCT06406114PHASE2RECRUITINGOptimizing the Diagnostic Approach to Cephalosporin Allergy Testing
NCT00143533PHASE1COMPLETEDPrevention of Diarrhea in Patients Taking IV Irinotecan for Relapsed or Difficult to Treat Pediatric Solid Tumors
NCT00194532Not specifiedCOMPLETEDCefpodoxime vs Ciprofloxacin for Acute Cystitis
NCT03098485Not specifiedCOMPLETEDHealthy Patients & Effect of Antibiotics

Clinical evidence (CIViC)

No CIViC predictive evidence (expected for non-precision-medicine drugs).

Pharmacology

Pharmacogenomics

No CPIC/DPWG dosing guideline or drug-level clinical/variant annotations in PharmGKB for this molecule.

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