Cefroxadine (CGP-9000), an orally active cephalosporin
- 1 July 1980
- journal article
- research article
- Published by American Society for Microbiology in Antimicrobial Agents and Chemotherapy
- Vol. 18 (1) , 105-110
- https://doi.org/10.1128/aac.18.1.105
Abstract
Cefroxadine (GCP-9000; CXD), 7 beta[D-2-amino-2-(1,4-cyclohexadienyl)-acetamido]-3-methoxy-ceph-3-em-carboxylic acid, is a new orally active cephalosporin derivative. The spectrum of antibacterial activity of CXD is identical with that of cephalexin (CEX), but CXD was twofold more effective than CEX against Escherichia coli and Klebsiella pneumoniae, CXD was as stable to penicillinase as CEX, but it was hydrolyzed by cephalosporinase, with a relative rate of hydrolysis similar to that of CEX. The affinities of CXD and CEX to penicillin-binding proteins of E. coli were estimated; the affinity of CXD to penicillin-binding protein 1Bs was higher than that of CEX. Consistent with this, CXD had more intensive lytic activity than CEX. In vivo antibacterial activities of CXD and CEX were compared using systemic infections of mice with E. coli and K. pneumoniae; CXD was consistently more active than CEX.This publication has 10 references indexed in Scilit:
- Isolation of a mutant of Escherichia coli lacking penicillin-sensitive D-alanine carboxypeptidase IA.Proceedings of the National Academy of Sciences, 1978
- Determination of the ID50 values of antibacterial agents in agar.The Journal of Antibiotics, 1978
- Thermosensitive mutation in Escherichia coli simultaneously causing defects in penicillin-binding protein-1Bs and in enzyme activity for peptidoglycan synthesis in vitro.Proceedings of the National Academy of Sciences, 1977
- Simultaneous deletion of D-alanine carboxypeptidase IB-C and penicillin-binding component IV in a mutant of Escherichia coli K12.Proceedings of the National Academy of Sciences, 1977
- Mutants of Escherichia coli lacking in highly penicillin-sensitive D-alanine carboxypeptidase activity.Proceedings of the National Academy of Sciences, 1977
- Plasmid-Mediated Penicillin Beta-Lactamases in Pseudomonas aeruginosaAntimicrobial Agents and Chemotherapy, 1976
- Distinct penicillin binding proteins involved in the division, elongation, and shape of Escherichia coli K12.Proceedings of the National Academy of Sciences, 1975
- Biochemical Properties of a Cephalosporin β‐Lactamase from Pseudomonas aeruginosaJapanese Journal of Microbiology, 1973