Cefotaxime Sodium

CHEMBL1010 Phase 4 已批准 Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
477.5 g/mol
LogP
Phase
4

The sodium salt formulation of cefotaxime is the standard parenteral preparation used in hospitals for serious and life-threatening infections including bacterial meningitis and gram-negative sepsis. Its broad spectrum and CNS penetration make it a first-line option in many clinical guidelines. Dose adjustment is required in severe renal impairment.

分子量

477.5000 g/mol

TPSA

230.00 Ų

治疗领域

作用机制

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)

机制

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.

二维结构

SVG PNG

Cite this structure


                        

Embed this structure


                        

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.[Na+]

InChI

InChI=1S/C16H17N5O7S2.Na/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);/q;+1/p-1/b20-9-;/t10-,14-;/m1./s1

Molecular Formula

C16H16N5NaO7S2

HBD / HBA

2 / 12

可旋转键数

8

重原子数

31

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.

常见问题

The sodium salt formulation of cefotaxime is the standard parenteral preparation used in hospitals for serious and life-threatening infections including bacterial meningitis and gram-negative sepsis. Its broad spectrum and CNS penetration make it a first-line option in many clinical guidelines. Dose adjustment is required in severe renal impairment.

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 Sodium 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). CHEMBL1010. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 10695961. Chemical information database.

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

医疗免责声明

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.