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Antimicrobial Agents and Chemotherapy, April 2003, p. 1447-1448, Vol. 47, No. 4
0066-4804/03/$08.00+0 DOI: 10.1128/AAC.47.4.1447-1448.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.
Division of Infectious Diseases, Department of Pediatrics, State University of New York Downstate Medical Center, Brooklyn, New York 11203-2098
Received 15 July 2002/ Returned for modification 9 November 2002/ Accepted 30 December 2002
The in vitro activity of NVP-PDF386 (VRC4887), a novel new peptide deformylase inhibitor, and those of levofloxacin and clarithromycin were tested against 21 isolates of Chlamydia pneumoniae. The MIC at which 90% of the isolates were inhibited and the minimal bactericidal concentration at which 90% of the isolates were killed by NVP-PDF386 for all isolates of C. pneumoniae were 0.008 µg/ml (range, 0.008 to 0.015 µg/ml) compared to 0.25 and 0.06 µg/ml for levofloxacin and clarithromycin, respectively.
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