
What are examples of beta-lactam antibiotics?
Answer
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Hint : Antibiotics with a beta-lactam ring in their molecular structure are known as beta-lactam antibiotics. The most commonly used antibiotic class is Beta-lactam antibiotics, which function by inhibiting bacterial cell wall biosynthesis.
Complete Step By Step Answer:
A lactam is a cyclic amide in which the N atom is bound to the chain's beta carbon to form a four-membered ring.
This is a function that all beta-lactam antibiotics share.
The central ring structures of beta-lactams are used to classify them.
1. Beta-lactam rings fused to a saturated five-membered ring
Penams: A thiazolidine ring fused to the Beta-lactam ring
Example: Penicillin G
2. Beta-lactam rings fused to unsaturated five-membered rings
Penems: A dihydrothiazole ring fused to the Beta-lactam ring
Example: Faropenem
Carbapenems: A dihydropyrrole ring fused to the Beta-lactam ring
Example: Meropenem
3. Beta-lactam rings fused to unsaturated six-membered rings
Cephems: A dihydrothiazine ring fused to the Beta-lactam ring
Example: Cefalexin
Carbacephems: A tetrahydropyridine ring fused to the Beta-lactam ring
Example: Loracarbef
Oxacephems: A dihydro oxazine ring fused to the Beta-lactam ring
Example: Flomoxef
Additional Information:
Bacteria often gain resistance to beta-lactam antibiotics by producing a beta-lactamase enzyme, which attacks the beta-lactam ring. Beta-lactam antibiotics can be combined with beta-lactamase inhibitors like clavulanic acid to overcome this resistance.
Note :
Beta-lactam antibiotics were originally only effective against Gram-positive bacteria, but the production of broad-spectrum beta-lactam antibiotics that are effective against a variety of Gram-negative bacteria has expanded their utility. Antibiotics belonging to the beta-lactam family are currently the most commonly used universal antibiotics.
Complete Step By Step Answer:
A lactam is a cyclic amide in which the N atom is bound to the chain's beta carbon to form a four-membered ring.
This is a function that all beta-lactam antibiotics share.
The central ring structures of beta-lactams are used to classify them.
1. Beta-lactam rings fused to a saturated five-membered ring
Penams: A thiazolidine ring fused to the Beta-lactam ring
Example: Penicillin G
2. Beta-lactam rings fused to unsaturated five-membered rings
Penems: A dihydrothiazole ring fused to the Beta-lactam ring
Example: Faropenem
Carbapenems: A dihydropyrrole ring fused to the Beta-lactam ring
Example: Meropenem
3. Beta-lactam rings fused to unsaturated six-membered rings
Cephems: A dihydrothiazine ring fused to the Beta-lactam ring
Example: Cefalexin
Carbacephems: A tetrahydropyridine ring fused to the Beta-lactam ring
Example: Loracarbef
Oxacephems: A dihydro oxazine ring fused to the Beta-lactam ring
Example: Flomoxef
Additional Information:
Bacteria often gain resistance to beta-lactam antibiotics by producing a beta-lactamase enzyme, which attacks the beta-lactam ring. Beta-lactam antibiotics can be combined with beta-lactamase inhibitors like clavulanic acid to overcome this resistance.
Note :
Beta-lactam antibiotics were originally only effective against Gram-positive bacteria, but the production of broad-spectrum beta-lactam antibiotics that are effective against a variety of Gram-negative bacteria has expanded their utility. Antibiotics belonging to the beta-lactam family are currently the most commonly used universal antibiotics.
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