Literature DB >> 15388472

Antipneumococcal activity of LBM415, a new peptide deformylase inhibitor, compared with those of other agents.

Lois M Ednie1, Glenn Pankuch, Peter C Appelbaum.   

Abstract

The MICs of LBM415, a new peptide diformylase inhibitor, were evaluated and ranged from 0.03 to 4.0 microg/ml for 300 pneumococci, irrespective of their beta-lactam, macrolide, and quinolone susceptibilities. By comparison, vancomycin, teicoplanin, linezolid, and quinupristin-dalfopristin were also active, with MICs </=2.0 microg/ml. Gatifloxacin and moxifloxacin were the most active quinolones tested, while the MICs of the beta-lactams rose with those of penicillin G. LBM415 at two times the MIC was bactericidal (99.9% killing) against six strains after 24 h.

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Year:  2004        PMID: 15388472      PMCID: PMC521909          DOI: 10.1128/AAC.48.10.4027-4032.2004

Source DB:  PubMed          Journal:  Antimicrob Agents Chemother        ISSN: 0066-4804            Impact factor:   5.191


  23 in total

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4.  In vitro activity of linezolid against multiply resistant Gram-positive clinical isolates.

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Journal:  Antimicrob Agents Chemother       Date:  1999-08       Impact factor: 5.191

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  10 in total

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4.  Comparative antimicrobial characterization of LBM415 (NVP PDF-713), a new peptide deformylase inhibitor of clinical importance.

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6.  In vivo characterization of the peptide deformylase inhibitor LBM415 in murine infection models.

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Review 7.  Multidrug-resistant Streptococcus pneumoniae infections: current and future therapeutic options.

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  10 in total

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