Author/Authors :
Claude A. Quesnelle، نويسنده , , Patrice Gill، نويسنده , , Stephan Roy، نويسنده , , Marco Dodier، نويسنده , , Anne Marinier، نويسنده , , Alain Martel، نويسنده , , Lawrence B. Snyder، نويسنده , , Stanley V. D’Andrea، نويسنده , , Joanne J. Bronson، نويسنده , , MaryBeth Frosco، نويسنده , , Danielle Beaulieu، نويسنده , , Glen A. Warr، نويسنده , , Ken L. DenBleyker، نويسنده , , Terry M. Stickle، نويسنده , , Hyekyung Yang، نويسنده , , Susan E. Chaniewski، نويسنده , , Cheryl A. Ferraro، نويسنده , , Dennis Taylor، نويسنده , , John W. Russell، نويسنده , , Kenneth S. Santone، نويسنده , , et al.، نويسنده ,
Abstract :
In an era of increasing resistance to classical antibacterial agents, the synthetic oxazolidinone series of antibiotics has attracted much interest. Zyvox™ was the first oxazolidinone to be approved for clinical use against infections caused by multi-drug resistant Gram-positive bacteria. In the course of studies directed toward the discovery of novel antibacterial agents, a new series of synthetic phenyl-isoxazolinone agents that displayed potent activity against Gram-positive bacterial strains was recently discovered at Bristol-Myers Squibb. Extensive investigation of various substitutions on the phenyl ring was then undertaken. We report here, the synthesis and antibacterial activity of a series of biaryl isoxazolinone compounds.