Cefmenoxime

CHEMBL1201224 Phase 4 Aprobado Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
511.6 g/mol
LogP
Phase
4

A third-generation parenteral cephalosporin antibiotic with broad-spectrum activity against gram-negative bacteria including Pseudomonas and Enterobacteriaceae. It is used for serious infections including respiratory, urinary, and intra-abdominal infections. Like some other cephalosporins, it contains an N-methylthiotetrazole side chain that may affect alcohol tolerance and vitamin K metabolism.

Peso molecular

511,6000 g/mol

LogP

0,00

TPSA

270,00 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

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SMILES

CO/N=C(\C(=O)N[C@@H]1C(=O)N2C(C(=O)O)=C(CSc3nnnn3C)CS[C@H]12)c1csc(N)n1

InChI

InChI=1S/C16H17N9O5S3/c1-24-16(20-22-23-24)33-4-6-3-31-13-9(12(27)25(13)10(6)14(28)29)19-11(26)8(21-30-2)7-5-32-15(17)18-7/h5,9,13H,3-4H2,1-2H3,(H2,17,18)(H,19,26)(H,28,29)/b21-8-/t9-,13-/m1/s1

Molecular Formula

C16H17N9O5S3

HBD / HBA

3 / 14

Enlaces Rotables

8

Átomos Pesados

33

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

A third-generation parenteral cephalosporin antibiotic with broad-spectrum activity against gram-negative bacteria including Pseudomonas and Enterobacteriaceae. It is used for serious infections including respiratory, urinary, and intra-abdominal infections. Like some other cephalosporins, it contains an N-methylthiotetrazole side chain that may affect alcohol tolerance and vitamin K metabolism.

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, Cefmenoxime 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). CHEMBL1201224. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 9570757. 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.