Ceforanide

CHEMBL1201046 Phase 4 Approuvé Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
519.6 g/mol
LogP
-3.2
Phase
4

A second-generation cephalosporin antibiotic used for the treatment of lower respiratory, urinary, skin, and bone infections caused by susceptible organisms. It has a relatively long half-life for its class, allowing twice-daily dosing. It is no longer widely used in clinical practice and has been largely replaced by newer antibiotics.

Masse moléculaire

519,6000 g/mol

LogP

-3,20

TPSA

244,00 Ų

Règle des 5 de Lipinski

Non conforme

Mécanisme d'action

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)

Mécanisme

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.

Structure 2D

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SMILES

NCc1ccccc1CC(=O)N[C@@H]1C(=O)N2C(C(=O)O)=C(CSc3nnnn3CC(=O)O)CS[C@H]12

InChI

InChI=1S/C20H21N7O6S2/c21-6-11-4-2-1-3-10(11)5-13(28)22-15-17(31)27-16(19(32)33)12(8-34-18(15)27)9-35-20-23-24-25-26(20)7-14(29)30/h1-4,15,18H,5-9,21H2,(H,22,28)(H,29,30)(H,32,33)/t15-,18-/m1/s1

Molecular Formula

C20H21N7O6S2

HBD / HBA

4 / 12

Liaisons Rotatives

10

Atomes Lourds

35

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.

Foire aux questions

A second-generation cephalosporin antibiotic used for the treatment of lower respiratory, urinary, skin, and bone infections caused by susceptible organisms. It has a relatively long half-life for its class, allowing twice-daily dosing. It is no longer widely used in clinical practice and has been largely replaced by newer antibiotics.

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, Ceforanide 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). CHEMBL1201046. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 43507. Chemical information database.

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

Avertissement médical

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.