Cephalosporins are a class of beta-lactam antibiotics. The antibiotic has the core four-membered β-lactam ring bonded to a six-membered dihydrothiazine ring. Cephalosporins inhibit the synthesis of the peptidoglycan layer of the bacterial cell wall by mimicking the D-Ala-D-Ala site of the peptidoglycan precursors preventing the binding of the penicillin-binding protein required for the synthesis of the bacterial cell wall.
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