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Oxazolidinones

Known as: Oxazolidinones [Chemical/Ingredient], oxazolidinone 
Derivatives of oxazolidin-2-one. They represent an important class of synthetic antibiotic agents.
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2011
Review
2011
  • L. Silver
  • Clinical Microbiology Reviews
  • 2011
  • Corpus ID: 27876920
SUMMARY The discovery of novel small-molecule antibacterial drugs has been stalled for many years. The purpose of this review is… Expand
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Review
2008
Review
2008
  • M. Roberts
  • FEMS microbiology letters
  • 2008
  • Corpus ID: 34744466
This Minireview summarizes the changes in the field of bacterial resistance to macrolide, lincosamide, streptogramin, ketolide… Expand
Highly Cited
2006
Highly Cited
2006
ABSTRACT A novel multidrug resistance phenotype mediated by the Cfr rRNA methyltransferase is observed in Staphylococcus aureus… Expand
Review
2004
Review
2004
Oxazolidinones are a new group of antibiotics. These synthetic drugs are active against a large spectrum of Gram-positive… Expand
Review
2003
Review
2003
The development of bacterial resistance to currently available antibacterial agents is a growing global health problem. Of… Expand
Review
2003
Review
2003
Each antimicrobial agent developed for clinical use during the past 60 years has ultimately encountered problems with the… Expand
Review
2002
Review
2002
SUMMARY The history, taxonomy, geographic distribution, clinical disease, and therapy of the pathogenic nonpigmented or late… Expand
Highly Cited
2001
Highly Cited
2001
Selective intramolecular alkane oxidations: an RhII carboxylate catalyzed C-H amination reaction facilitates the preparation of 1… Expand
Highly Cited
1998
Highly Cited
1998
ABSTRACT The oxazolidinones represent a new class of antimicrobial agents which are active against multidrug-resistant… Expand
Highly Cited
1996
Highly Cited
1996
Bacterial resistance development has become a very serious clinical problem for many classes of antibiotics. The 3-aryl-2… Expand