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Third generation cephalosporins

Wyeth is now a wholly owned subsidiary of Pfizer · FDA-approved active Small molecule

Third-generation cephalosporins inhibit bacterial cell wall synthesis by binding to penicillin-binding proteins and blocking cross-linking of peptidoglycan.

Third-generation cephalosporins inhibit bacterial cell wall synthesis by binding to penicillin-binding proteins and blocking cross-linking of peptidoglycan. Used for Bacterial infections caused by susceptible gram-positive and gram-negative organisms, Respiratory tract infections, Urinary tract infections.

At a glance

Generic nameThird generation cephalosporins
SponsorWyeth is now a wholly owned subsidiary of Pfizer
Drug classBeta-lactam antibiotic (cephalosporin)
TargetPenicillin-binding proteins (PBPs)
ModalitySmall molecule
Therapeutic areaInfectious Disease
PhaseFDA-approved

Mechanism of action

These beta-lactam antibiotics penetrate the bacterial cell wall and covalently bind to penicillin-binding proteins, preventing the cross-linking of peptidoglycan strands essential for cell wall integrity. This leads to cell wall weakening, osmotic instability, and bacterial cell lysis. Third-generation cephalosporins have enhanced activity against gram-negative organisms and improved beta-lactamase stability compared to earlier generations.

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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