Synthesis and in vitro activity of novel isoxazolyl tetrahydropyridinyl oxazolidinone antibacterial agents |
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Authors: | Lee Jae Seok Cho Yong Seo Chang Moon Ho Koh Hun Yeong Chung Bong Young Pae Ae Nim |
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Affiliation: | Biochemicals Research Center, Korea Institute of Science and Technology, Cheongryang, Seoul 130-650, South Korea. |
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Abstract: | ![](https://cache.aipub.cn/cache?img_url=https://ars.els-cdn.com/content/image/1-s2.0-S0960894X03008448-fx7056.gif) A series of isoxazolyl tetrahydropyridinyl oxazolidinones with various substituents at the 3-position of the isoxazole ring have been synthesized and their in vitro antibacterial activities (MIC) were evaluated against several Gram-positive strains including the resistant strains of Staphyloccus and Enterococcus, such as MRSA and VRE. One of the most potent compounds synthesized, 4f, showed comparable or better activity against selected bacterial strains than those of linezolid and vancomycin. |
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