Affiliation:
1. Medical Research Laboratores, Pfizer Inc., Groton, Connecticut 06340
Abstract
In the new agent 3-(5-tetrazolyl)penam, hereafter referred to as CP-35,587, the carboxyl function at C3 in the penicillin nucleus has been replaced with the 5-tetrazolyl moiety. Marked changes in spectrum and resistance to gram-negative β-lactamases, particularly with regard to
Klebsiella pneumoniae
isolates, were conferred by this modification. The anti-
Klebsiella
activity clearly distinguishes the antibacterial spectrum of CP-35,587 from any known broad-spectrum penicillin. Compared to orally active cephalosporins, the spectrum advantage of CP-35,587 encompasses
Enterobacter, Serratia marcescens, Citrobacter, Providencia, Haemophilus influenzae
, and
Streptococcus faecalis
, both in vitro and in murine infections produced by many of the above-named microorganisms. Thus, CP-35,587 combines and extends the antibacterial activity of broad-spectrum penicillins and orally active cephalosporins.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Pharmacology (medical),Pharmacology
Reference10 articles.
1. Batmon H. E. 1957. An introduction to statistics in the medical sciences p. 64-67. Burgess Publishing Co. Minneapolis.
2. Carbenicillin indanyl sodium, an orally active derivative of carbenicillin;English A. R.;Antimicrob. Agents Chemother.,1972
3. Antibiotic sensitivity testing- report of international collaborative study. Acta;Ericsson H. M.;Pathol. Microbiol. Scand. Sect. B,1971
4. Total synthesis of Bisnorpenicillin V;Hoogmartens J.;J. Med. Chem.,1974
5. Huang H. T. T. A. Seto J. M. Weaver A. R. English T. J. McBride and G. M. Shull. 1964. Antibiotic properties of a-substituted penicillin amides against penicillin-resistant staphylococci p. 493-499. Antimicrob. Agents Chemother. 1963.
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