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In vitro activity of ramoplanin against vancomycin-resistant gram-positive organisms.

Abstract
In vitro activity of ramoplanin, a cyclic lipoglycopeptide, against 92 vancomycin-resistant gram-positive organisms was evaluated. Ramoplanin demonstrated potent activity against many highly vancomycin-resistant organisms including enterococci (MICs for 90% of strains tested of 0.5 micrograms/ml) and against Lactobacillus spp., Leuconostoc spp., and Pediococcus spp., all of which were inhibited at concentrations of < or = 0.25 micrograms/ml. This drug or a derivative compound merits further investigation as a potential therapeutic agent for infections due to vancomycin-resistant enterococci.
AuthorsL A Collins, G M Eliopoulos, C B Wennersten, M J Ferraro, R C Moellering Jr
JournalAntimicrobial agents and chemotherapy (Antimicrob Agents Chemother) Vol. 37 Issue 6 Pg. 1364-6 (Jun 1993) ISSN: 0066-4804 [Print] United States
PMID8328787 (Publication Type: Comparative Study, Journal Article)
Chemical References
  • Anti-Bacterial Agents
  • Depsipeptides
  • Peptides, Cyclic
  • ramoplanin
  • Vancomycin
Topics
  • Anti-Bacterial Agents (pharmacology)
  • Depsipeptides
  • Drug Resistance, Microbial
  • Enterococcus (drug effects)
  • Gram-Positive Bacteria (drug effects)
  • Humans
  • Kinetics
  • Microbial Sensitivity Tests
  • Peptides, Cyclic
  • Vancomycin (pharmacology)

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