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β-lactam antibiotic

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Also known as β-lactam antibiotics, beta-lactam antibiotics, beta-lactam antibiotic, β-lactam, beta-lactam

class of broad-spectrum antibiotics, consisting of all antibiotic agents that contain a β-lactam ring in their molecular structures

Key facts

Use
Bacterial infection
Atc code
J01C
Biological target
Penicillin binding protein
Mesh
D047090

via Wikipedia infobox

Research

13,481 papers

via PubMed

~17 min read

Encyclopedic overview

β-Lactam antibiotics (beta-lactam antibiotics) are antibiotics that contain a β-lactam ring in their chemical structure. This includes penicillin derivatives (penams), cephalosporins and cephamycins (cephems), monobactams, carbapenems and carbacephems. Most β-lactam antibiotics work by inhibiting cell wall biosynthesis in the bacterial organism and are the most widely used group of antibiotics. Until 2003, when measured by sales, more than half of all commercially available antibiotics in use were β-lactam compounds. The first β-lactam antibiotic discovered, penicillin, was isolated from a strain of Penicillium rubens (named as Penicillium notatum at the time).

Bacteria often develop resistance to β-lactam antibiotics by synthesizing a β-lactamase, an enzyme that attacks the β-lactam ring. To overcome this resistance, β-lactam antibiotics can be given with β-lactamase inhibitors such as clavulanic acid.

Excerpted from Wikipedia’s “β-lactam antibiotic” article, available under the CC BY-SA 4.0 licence.