Cefonicid

CHEMBL1601 Phase 4 Zugelassen Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
542.6 g/mol
LogP
-1.9
Phase
4

A second-generation cephalosporin antibiotic with a prolonged half-life that allows for once-daily intramuscular dosing, used for mild to moderate infections and surgical prophylaxis. It is effective against many gram-positive and gram-negative bacteria. Its extended dosing interval offers practical convenience in outpatient parenteral antibiotic therapy.

Molekularmasse

542,6000 g/mol

LogP

-1,90

TPSA

264,00 Ų

Lipinski-Regel der Fünf

Nicht bestanden

Wirkmechanismus

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)

Mechanismus

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.

2D-Struktur

SVG PNG

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SMILES

O=C(O)C1=C(CSc2nnnn2CS(=O)(=O)O)CS[C@@H]2[C@H](NC(=O)[C@H](O)c3ccccc3)C(=O)N12

InChI

InChI=1S/C18H18N6O8S3/c25-13(9-4-2-1-3-5-9)14(26)19-11-15(27)24-12(17(28)29)10(6-33-16(11)24)7-34-18-20-21-22-23(18)8-35(30,31)32/h1-5,11,13,16,25H,6-8H2,(H,19,26)(H,28,29)(H,30,31,32)/t11-,13-,16-/m1/s1

Molecular Formula

C18H18N6O8S3

HBD / HBA

4 / 13

Rotierbare Bindungen

9

Schwere Atome

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.

Häufig gestellte Fragen

A second-generation cephalosporin antibiotic with a prolonged half-life that allows for once-daily intramuscular dosing, used for mild to moderate infections and surgical prophylaxis. It is effective against many gram-positive and gram-negative bacteria. Its extended dosing interval offers practical convenience in outpatient parenteral antibiotic therapy.

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, Cefonicid 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). CHEMBL1601. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 43594. Chemical information database.

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

Medizinischer Haftungsausschluss

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.