| Literature DB >> 17988109 |
Toni-Jo Poel1, Richard C Thomas, Wade J Adams, Paul A Aristoff, Michael R Barbachyn, Frederick E Boyer, Joan Brieland, Roger Brideau, Joanne Brodfuehrer, Alan P Brown, Allison L Choy, Michael Dermyer, Michael Dority, Charles W Ford, Robert C Gadwood, Debra Hanna, Cai Hongliang, Michael D Huband, Christopher Huber, Rose Kelly, Ji-Young Kim, Joseph P Martin, Paul J Pagano, Daniel Ross, Laura Skerlos, Mark C Sulavik, Tong Zhu, Gary E Zurenko, J V N Vara Prasad.
Abstract
Oxazolidinones possessing a C-5 carboxamide functionality (reverse amides) represent a new series of compounds that block bacterial protein synthesis. These reverse amides also exhibited less potency against monoamine oxidase (MAO) enzymes and thus possess less potential for the side effects associated with MAO inhibition. The title compound (14) showed reduced in vivo myelotoxicity compared to linezolid in a 14-day safety study in rats, potent in vivo efficacy in murine systemic infection models, and excellent pharmacokinetic properties.Entities:
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Year: 2007 PMID: 17988109 DOI: 10.1021/jm070708p
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446