Cephalexin

CHEMBL1200544 Phase 4 Aprobado Small molecule
Half-Life
0.5-1.2 hours
Bioavailability
Protein Binding
Molecular Weight
347.4 g/mol
LogP
0.6
Phase
4

A first-generation oral cephalosporin antibiotic that inhibits bacterial cell wall synthesis, used for skin and soft tissue infections, respiratory tract infections, urinary tract infections, and streptococcal pharyngitis. It is particularly effective against gram-positive organisms such as Staphylococcus and Streptococcus species. It is generally well tolerated and widely used in community medicine.

Peso molecular

347,3890 g/mol

LogP

0,60

TPSA

138,00 Ų

Regla de cinco de Lipinski

Cumple

Áreas terapéuticas

Clases de fármacos

Mecanismo de acción

First-generation cephalosporin inhibiting cell wall synthesis.

Pharmacokinetics (PK)

Half-Life 0.5-1.2 hours

Pharmacodynamics (PD)

Mecanismo

First-generation cephalosporin inhibiting cell wall synthesis.

Estructura 2D

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SMILES

CC1=C(C(=O)O)N2C(=O)[C@@H](NC(=O)[C@H](N)c3ccccc3)[C@H]2SC1.O

InChI

InChI=1S/C16H17N3O4S.H2O/c1-8-7-24-15-11(14(21)19(15)12(8)16(22)23)18-13(20)10(17)9-5-3-2-4-6-9;/h2-6,10-11,15H,7,17H2,1H3,(H,18,20)(H,22,23);1H2/t10-,11-,15-;/m1./s1

Molecular Formula

C16H17N3O4S

HBD / HBA

3 / 6

Enlaces Rotables

4

Átomos Pesados

24

Primary Target

No side effects recorded

Side effect data is not yet available for this drug.

Preguntas frecuentes

A first-generation oral cephalosporin antibiotic that inhibits bacterial cell wall synthesis, used for skin and soft tissue infections, respiratory tract infections, urinary tract infections, and streptococcal pharyngitis. It is particularly effective against gram-positive organisms such as Staphylococcus and Streptococcus species. It is generally well tolerated and widely used in community medicine.

First-generation cephalosporin inhibiting cell wall synthesis.

Key pharmacokinetic parameters for Cephalexin: Half-life: 0.5-1.2 hours.

Yes, Cephalexin is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.

Related Drugs

{# 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). CHEMBL1200544. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 27447. 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.