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SUBSTITUTED PHENYLOXAZOLIDINONES FOR ANTIMICROBIAL THERAPY

机译:取代的苯氧氮唑烷酮用于抗微生物治疗

摘要

The present invention relates to novel oxazolidinones (Formula I): or a pharmaceutically acceptable salt having ring A characterized by N-containing monocyclic, bicyclic or spirocyclic substituents, to their preparation, and to their use as drugs for treating Mycobacterium tuberculosis and other microbial infections, either alone or in combination with other anti-infective treatments.
机译:本发明涉及新的恶唑烷酮(式I):或具有环A的药学上可接受的盐,其特征在于含N-单环,双环或丝环取代基,它们的制备和它们用作治疗结核病和其他微生物感染的药物和其它微生物感染的药物 ,单独或与其他抗感染治疗组合。

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