Cefditoren Pivoxil

CHEMBL454446 Phase 4 Aprobado Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
620.7 g/mol
LogP
4.7
Phase
4

An oral third-generation cephalosporin antibiotic prodrug that is hydrolyzed in the intestinal wall to the active cefditoren. It is used to treat community-acquired pneumonia, acute exacerbations of chronic bronchitis, and skin infections. The pivoxil moiety releases pivalic acid during absorption, which may interfere with carnitine metabolism with prolonged use.

Peso molecular

620,7000 g/mol

LogP

4,70

TPSA

257,00 Ų

Regla de cinco de Lipinski

No cumple

Mecanismo de acción

Disrupts bacterial cell wall synthesis by binding to penicillin-binding proteins (PBPs), inhibiting the final transpeptidation step of peptidoglycan synthesis. The resulting cell wall defects cause osmotic instability and bacteriolysis.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Mecanismo

Disrupts bacterial cell wall synthesis by binding to penicillin-binding proteins (PBPs), inhibiting the final transpeptidation step of peptidoglycan synthesis. The resulting cell wall defects cause osmotic instability and bacteriolysis.

Estructura 2D

SVG PNG

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SMILES

CO/N=C(\C(=O)N[C@@H]1C(=O)N2C(C(=O)OCOC(=O)C(C)(C)C)=C(/C=C\c3scnc3C)CS[C@H]12)c1csc(N)n1

InChI

InChI=1S/C25H28N6O7S3/c1-12-15(41-10-27-12)7-6-13-8-39-21-17(29-19(32)16(30-36-5)14-9-40-24(26)28-14)20(33)31(21)18(13)22(34)37-11-38-23(35)25(2,3)4/h6-7,9-10,17,21H,8,11H2,1-5H3,(H2,26,28)(H,29,32)/b7-6-,30-16-/t17-,21-/m1/s1

Molecular Formula

C25H28N6O7S3

HBD / HBA

2 / 14

Enlaces Rotables

12

Átomos Pesados

41

No targets recorded

Target interaction data is not yet available for this drug.

No interactions recorded

Drug interaction data is not yet available for this compound.

No side effects recorded

Side effect data is not yet available for this drug.

Preguntas frecuentes

An oral third-generation cephalosporin antibiotic prodrug that is hydrolyzed in the intestinal wall to the active cefditoren. It is used to treat community-acquired pneumonia, acute exacerbations of chronic bronchitis, and skin infections. The pivoxil moiety releases pivalic acid during absorption, which may interfere with carnitine metabolism with prolonged use.

Disrupts bacterial cell wall synthesis by binding to penicillin-binding proteins (PBPs), inhibiting the final transpeptidation step of peptidoglycan synthesis. The resulting cell wall defects cause osmotic instability and bacteriolysis.

Yes, Cefditoren Pivoxil is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.

{# References & Data Sources section for drug detail pages. Renders standard pharmacological database links plus the drug's data_sources field. #}

References & Data Sources

  • ChEMBL — European Bioinformatics Institute (EBI). CHEMBL454446. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 6437877. Chemical information database.

Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.

Aviso médico

This content is for educational and informational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment. Always consult a qualified healthcare provider before making medication decisions.

Data sources: ChEMBL, PubChem, DailyMed.