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Journal of Antimicrobial Chemotherapy (1988) 21, 711-720
© 1988 The British Society for Antimicrobial Chemotherapy


research-article

In-vitro microbiological activities of DuP 105 and DuP 721, novel synthetic oxazolidinones

W. Brumfitt and J. M. T. Hamilton-Miller

Department of Medical Microbiology, The Royal Free Hospital Medical School Pond Street, Hampstead, London NW3 2QG, UK

Received 23 December 1987; accepted 15 February 1988


DuP 105 and 721, synthetic antibiotics belonging to a totally novel chemical class (oxazolidinones), have been found to be active in vitro against a wide range of Gram-positive bacteria, including methicillin-resistant Staphylococcus aureus. DuP 721 had geometric mean MICs ranging from 1·1 to 16 mg/l against 167 strains of Staph. aureus, Staph. epidermidis, Staph. saprophyticus, streptococci of Groups A, B and D and diphtheroids. DuP 105 was between 1·5 and eight-fold less active. Bacteroides fragilis strains were also susceptible to the DuP compounds (mean MICs being 8·3 and 14·9 mg/l for DuP 721 and 105, respectively), but other Gram-negative species and yeasts were not inhibited' by concentrations in excess of 100 mg/l. Both compounds had a predominantly bacteriostatic action. No primary resistance was found, and the incidence of resistant variants in 105 strains tested was less than 1 per 103 bacteria.


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