Cephalexin

CHEMBL1200544 Phase 4 अनुमोदित 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.

आणविक भार

347.3890 g/mol

LogP

0.60

TPSA

138.00 Ų

लिपिंस्की RO5

उत्तीर्ण

चिकित्सीय क्षेत्र

दवा वर्ग

क्रिया का तंत्र

First-generation cephalosporin inhibiting cell wall synthesis.

Pharmacokinetics (PK)

Half-Life 0.5-1.2 hours

Pharmacodynamics (PD)

तंत्र

First-generation cephalosporin inhibiting cell wall synthesis.

2D संरचना

SVG PNG

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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

घूर्णनीय बंधन

4

भारी परमाणु

24

No side effects recorded

Side effect data is not yet available for this drug.

अक्सर पूछे जाने वाले प्रश्न

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.

चिकित्सा अस्वीकरण

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.