In vitro evaluation of DuP 105 and DuP 721, two new oxazolidinone antimicrobial agents

Antimicrob Agents Chemother. 1988 Jan;32(1):150-2. doi: 10.1128/AAC.32.1.150.

Abstract

DuP 105 and DuP 721 are two members of the oxazolidinones, a new class of synthetic antimicrobial agents with activity against gram-positive bacteria. In vitro tests compared the two new drugs with five other antimicrobial agents against 216 gram-positive isolates representing 4 genera and 10 species. DuP 721 MICs for 50% of the strains tested (MIC50s) ranged from 2.0 to 8.0 micrograms/ml, DuP 105 MIC50S ranged from 4.0 to 16 micrograms/ml, and vancomycin MIC50S ranged from 0.25 to 1.0 microgram/ml. Methicillin-resistant and -susceptible staphylococci were susceptible to ciprofloxacin, vancomycin, and DuP 721.

Publication types

  • Comparative Study

MeSH terms

  • Ampicillin / pharmacology
  • Anti-Bacterial Agents / pharmacology*
  • Cefaclor / pharmacology
  • Chemical Phenomena
  • Chemistry
  • Ciprofloxacin / pharmacology
  • Erythromycin / pharmacology
  • Gram-Positive Bacteria / drug effects*
  • Oxazoles / pharmacology*
  • Oxazolidinones
  • Vancomycin / pharmacology

Substances

  • Anti-Bacterial Agents
  • Oxazoles
  • Oxazolidinones
  • 4-acetylphenyloxooxazolidinylmethylacetamide
  • Ciprofloxacin
  • Erythromycin
  • Cefaclor
  • Vancomycin
  • Ampicillin
  • 4-methylsulfinylphenyloxooxazolidinylmethylacetamide