Cefotaxime

CHEMBL1730 Phase 4 Disetujui Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
455.5 g/mol
LogP
-1.4
Phase
4

A third-generation cephalosporin antibiotic with broad-spectrum activity against gram-negative bacteria and many gram-positive organisms, widely used for meningitis, sepsis, and serious respiratory and urinary tract infections. It penetrates the blood-brain barrier effectively, making it valuable in central nervous system infections. It is metabolized to desacetylcefotaxime, which retains some antibacterial activity.

Berat Molekul

455,5000 g/mol

LogP

-1,40

TPSA

227,00 Ų

Lipinski RO5

Lulus

Area Terapeutik

Mekanisme Kerja

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)

Mekanisme

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.

Struktur 2D

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SMILES

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

InChI

InChI=1S/C16H17N5O7S2/c1-6(22)28-3-7-4-29-14-10(13(24)21(14)11(7)15(25)26)19-12(23)9(20-27-2)8-5-30-16(17)18-8/h5,10,14H,3-4H2,1-2H3,(H2,17,18)(H,19,23)(H,25,26)/b20-9-/t10-,14-/m1/s1

Molecular Formula

C16H17N5O7S2

HBD / HBA

3 / 12

Ikatan yang Dapat Dirotasi

8

Atom Berat

30

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.

Pertanyaan yang Sering Diajukan

A third-generation cephalosporin antibiotic with broad-spectrum activity against gram-negative bacteria and many gram-positive organisms, widely used for meningitis, sepsis, and serious respiratory and urinary tract infections. It penetrates the blood-brain barrier effectively, making it valuable in central nervous system infections. It is metabolized to desacetylcefotaxime, which retains some antibacterial activity.

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, Cefotaxime 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). CHEMBL1730. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 5742673. Chemical information database.

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

Penyangkalan Medis

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.