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Antimicrobial Agents and Chemotherapy logoLink to Antimicrobial Agents and Chemotherapy
. 1991 Jan;35(1):141–146. doi: 10.1128/aac.35.1.141

In vitro antibacterial activities of PD 131628, a new 1,8-naphthyridine anti-infective agent.

M A Cohen 1, M D Huband 1, G B Mailloux 1, S L Yoder 1, G E Roland 1, J M Domagala 1, C L Heifetz 1
PMCID: PMC244955  PMID: 2014970

Abstract

PD 131628 is a new aminopyrrolidine-substituted fluorocyclopropyl naphthyridine quinolone which possesses high in vitro activity against a wide spectrum of bacterial species. The MICs for greater than or equal to 90% of strains were 0.125 to 0.25 microgram/ml for staphylococci, Streptococcus pyogenes, and S. pneumoniae; 0.5 micrograms/ml for S. agalactiae and Enterococcus faecalis; 0.125 micrograms/ml for members of the family Enterobacteriaceae and Acinetobacter spp.; 0.5 micrograms/ml for Pseudomonas aeruginosa; and less than or equal to 0.03 micrograms/ml for Haemophilus influenzae, Moraxella (Branhamella) catarrhalis, and Neisseria gonorrhoeae. In these in vitro comparisons with ciprofloxacin, PD 131628 is more active against gram-positive organisms, approximately equivalent against gram-negative organisms, and, like most other quinolones, relatively inactive against gram-negative anaerobes. In most instances, the in vitro potency of PD 131628 exceeded those of widely used compounds: ciprofloxacin, imipenem, ampicillin, penicillin G, oxacillin, cefazolin, ceftazidime, cefoxitin, cefsulodin, aztreonam, piperacillin, amikacin, spectinomycin, doxycycline, erythromycin, metronidazole, and vancomycin.

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Selected References

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  1. Chu D. T., Fernandes P. B. Structure-activity relationships of the fluoroquinolones. Antimicrob Agents Chemother. 1989 Feb;33(2):131–135. doi: 10.1128/aac.33.2.131. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Heifetz C. L., Bien P. A., Cohen M. A., Dombrowski M. E., Griffin T. J., Malta T. E., Sesnie J. C., Shapiro M. A., Wold S. A. Enoxacin: in-vitro and animal evaluation as a parenteral and oral agent against hospital bacterial isolates. J Antimicrob Chemother. 1988 Feb;21 (Suppl B):29–42. doi: 10.1093/jac/21.suppl_b.29. [DOI] [PubMed] [Google Scholar]
  3. Hoban D. J. Comparative in vitro activity of quinolones. Clin Invest Med. 1989 Feb;12(1):10–13. [PubMed] [Google Scholar]
  4. Neuman M., Esanu A. Gaps and perspectives of new fluoroquinolones. Drugs Exp Clin Res. 1988;14(6):385–391. [PubMed] [Google Scholar]
  5. Rosen T., Chu D. T., Lico I. M., Fernandes P. B., Marsh K., Shen L., Cepa V. G., Pernet A. G. Design, synthesis, and properties of (4S)-7-(4-amino-2-substituted-pyrrolidin-1-yl)quinolone-3-carboxylic acids. J Med Chem. 1988 Aug;31(8):1598–1611. doi: 10.1021/jm00403a020. [DOI] [PubMed] [Google Scholar]
  6. Sanchez J. P., Domagala J. M., Hagen S. E., Heifetz C. L., Hutt M. P., Nichols J. B., Trehan A. K. Quinolone antibacterial agents. Synthesis and structure-activity relationships of 8-substituted quinoline-3-carboxylic acids and 1,8-naphthyridine-3-carboxylic acids. J Med Chem. 1988 May;31(5):983–991. doi: 10.1021/jm00400a016. [DOI] [PubMed] [Google Scholar]
  7. Shapiro M. A., Heifetz C. L., Sesnie J. C. Comparison of microdilution and agar dilution procedures for testing antibiotic susceptibility of Neisseria gonorrhoeae. J Clin Microbiol. 1984 Oct;20(4):828–830. doi: 10.1128/jcm.20.4.828-830.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Wolfson J. S., Hooper D. C. The fluoroquinolones: structures, mechanisms of action and resistance, and spectra of activity in vitro. Antimicrob Agents Chemother. 1985 Oct;28(4):581–586. doi: 10.1128/aac.28.4.581. [DOI] [PMC free article] [PubMed] [Google Scholar]

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