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Antimicrobial Agents and Chemotherapy, August 2009, p. 3544-3548, Vol. 53, No. 8
0066-4804/09/$08.00+0 doi:10.1128/AAC.00400-09
Copyright © 2009, American Society for Microbiology. All Rights Reserved.

Department of Medical Microbiology and Infectious Diseases, Faculty of Medicine, University of Manitoba, Winnipeg, Manitoba, Canada,1 Affinium Pharmaceuticals, Inc., Toronto, Ontario, Canada2
Received 25 March 2009/ Returned for modification 9 May 2009/ Accepted 23 May 2009
AFN-1252, a potent inhibitor of enoyl-acyl carrier protein reductase (FabI), inhibited all clinical isolates of Staphylococcus aureus (n = 502) and Staphylococcus epidermidis (n = 51) tested, including methicillin (meticillin)-resistant isolates, at concentrations of
0.12 µg/ml. In contrast, AFN-1252 was inactive (MIC90, >4 µg/ml) against clinical isolates of Streptococcus pneumoniae, beta-hemolytic streptococci, Enterococcus spp., Enterobacteriaceae, nonfermentative gram-negative bacilli, and Moraxella catarrhalis. These data support the continued development of AFN-1252 for the treatment of patients with resistant staphylococcal infections.
Published ahead of print on 1 June 2009.
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