Activities of RPR 106972 (a new oral streptogramin), cefditoren (a new oral cephalosporin), two new oxazolidinones (U-100592 and U-100766), and other oral and parenteral agents against 203 penicillin-susceptible and -resistant pneumococci

Antimicrob Agents Chemother. 1996 Feb;40(2):481-4. doi: 10.1128/AAC.40.2.481.

Abstract

Agar dilution was used to determine the MICs of RPR 106972 (a new oral streptogramin), cefditoren (a new oral cephalosporin), two new oxazolidinones (U-100592 and U-100766), and other oral and parenteral agents for 203 penicillin-susceptible and -resistant pneumococci. All pneumococci were inhibited by RPR 106972 at < or = 0.5 microgram/ml. Cefditoren was very active against all pneumococcal groups, with MICs of < or = 2.0 micrograms/ml. Amoxicillin with or without clavulanate was the next most active oral beta-lactam, followed by cefdinir, cefuroxime, cefpodoxime, and cefprozil. U-100592 and U-100766 were very active against all classes of pneumococci, with all MICs < or = 1.0 microgram/ml.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetamides / pharmacology
  • Amino Acid Sequence
  • Anti-Bacterial Agents / pharmacology*
  • Cephalosporins / pharmacology*
  • Linezolid
  • Microbial Sensitivity Tests
  • Molecular Sequence Data
  • Oxazoles / pharmacology
  • Oxazolidinones*
  • Penicillin Resistance
  • Streptococcus pneumoniae / drug effects*
  • Virginiamycin / chemistry
  • Virginiamycin / pharmacology

Substances

  • Acetamides
  • Anti-Bacterial Agents
  • Cephalosporins
  • Oxazoles
  • Oxazolidinones
  • RPR 106972
  • Virginiamycin
  • cefditoren
  • eperezolid
  • Linezolid