Beta-lactam antibiotics
From Proteopedia
(Difference between revisions)
(2 intermediate revisions not shown.) | |||
Line 1: | Line 1: | ||
<StructureSection load='1ceg' size='340' side='right' caption='D-alanyl-D-alanine carboxipeptidase transpeptidase complex with cephalothin (PDB code [[1ceg]])' scene=''> | <StructureSection load='1ceg' size='340' side='right' caption='D-alanyl-D-alanine carboxipeptidase transpeptidase complex with cephalothin (PDB code [[1ceg]])' scene=''> | ||
- | β-lactam antibiotics (beta-lactam antibiotics) are antibiotics that contain a beta-lactam ring in their chemical structure. This includes [[Penams|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. See also [https://en.wikipedia.org/wiki/Beta-lactam_antibiotics Beta-lactam antibiotics]. | + | β-lactam antibiotics (beta-lactam antibiotics) are antibiotics that contain a beta-lactam ring in their chemical structure. This includes [[Penams|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. See also [https://en.wikipedia.org/wiki/Beta-lactam_antibiotics Beta-lactam antibiotics]. |
*[[How B-lactam drugs work]] | *[[How B-lactam drugs work]] |
Current revision
|