In vitro biological activities of 6-isosteric penicillins and 7-isosteric cephalosporins

J Antibiot (Tokyo). 1984 Nov;37(11):1441-8. doi: 10.7164/antibiotics.37.1441.

Abstract

Antibiotic and penicillinase inhibitor activities of various penicillin and cephalosporin analogs are reported. The compounds include C-6 penicillin and C-7 cephalosporin carbon, oxygen and sulfur analogs obtained by replacing the NH of the amide side chains with CH2, O and S, respectively. In almost all cases, analogs were considerably less active than the standard compounds (benzylpenicillin and cephalothin). However, some of the analogs act as penicillinase inhibitors.

MeSH terms

  • Bacteria / drug effects*
  • Cephalosporins / pharmacology*
  • Microbial Sensitivity Tests
  • Penicillins / pharmacology*
  • beta-Lactamase Inhibitors

Substances

  • Cephalosporins
  • Penicillins
  • beta-Lactamase Inhibitors