FUSED RING-CONTAINING OXAZOLIDINONES ANTIBIOTICS
    2.
    发明申请
    FUSED RING-CONTAINING OXAZOLIDINONES ANTIBIOTICS 有权
    含氟环氧化亚油酸酯抗生素

    公开(公告)号:US20140243288A1

    公开(公告)日:2014-08-28

    申请号:US14347595

    申请日:2012-09-29

    发明人: Hui Zhang Aichen Wang

    摘要: The present invention relates to a fused ring-containing oxazolidinone compound shown by general formula (I), a pharmaceutically acceptable salt thereof and a stereoisomer thereof, wherein R1, R2, R3, R4, R5, R6, A, B and C are as defined in the description. The present invention further relates to a method for preparing the compound, a pharmaceutical composition and a pharmaceutical formulation comprising the compound, and a use of the compound for the manufacture of a medicament for the treatment and/or prevention of infectious diseases and a use for the treatment and/or prevention of infectious diseases.

    摘要翻译: 本发明涉及通式(I)所示的稠环恶唑烷酮化合物,其药学上可接受的盐和立体异构体,其中R1,R2,R3,R4,R5,R6,A,B和C为 在说明书中定义。 本发明还涉及一种制备化合物的方法,药物组合物和包含该化合物的药物制剂,以及该化合物在制备用于治疗和/或预防感染性疾病的药物中的用途,以及用于 治疗和/或预防传染病。

    BIARYL HETEROCYCLE SUBSTITUTED OXAZOLIDINONE ANTIBACTERIAL AGENTS
    5.
    发明申请
    BIARYL HETEROCYCLE SUBSTITUTED OXAZOLIDINONE ANTIBACTERIAL AGENTS 有权
    二异氰酸酯替代奥昔洛芬抗体药剂

    公开(公告)号:US20140235584A1

    公开(公告)日:2014-08-21

    申请号:US14347583

    申请日:2012-09-28

    发明人: Frank Wu Aichen Wang

    摘要: The present invention relates to a biaryl heterocycle substituted oxazolidinone antibacterials shown by general formula (I), a pharmaceutically acceptable salt thereof, an isomer or a prodrug thereof, wherein R1, R2, R3, R4, R5, A and B are as defined in the description. The present invention further relates to a method for preparing the compound, a pharmaceutical composition and a pharmaceutical formulation comprising the compound, and a use of the compound in the manufacture of a medicament for the treatment and/or prevention of infectious diseases and a use for the treatment and/or prevention of infectious diseases.

    摘要翻译: 本发明涉及由通式(I)表示的联芳基杂环取代的恶唑烷酮抗菌剂,其药学上可接受的盐,异构体或前药,其中R 1,R 2,R 3,R 4,R 5,A和B如 说明。 本发明还涉及制备化合物的方法,药物组合物和包含该化合物的药物制剂,以及该化合物在制备用于治疗和/或预防感染性疾病的药物中的用途,以及用于 治疗和/或预防传染病。

    Biaryl heterocycle substituted oxazolidinone antibacterial agents
    7.
    发明授权
    Biaryl heterocycle substituted oxazolidinone antibacterial agents 有权
    双芳基杂环取代恶唑烷酮抗菌剂

    公开(公告)号:US09359344B2

    公开(公告)日:2016-06-07

    申请号:US14347583

    申请日:2012-09-28

    发明人: Frank Wu Aichen Wang

    摘要: The present invention relates to a biaryl heterocycle substituted oxazolidinone antibacterials shown by general formula (I), a pharmaceutically acceptable salt thereof, an isomer or a prodrug thereof, wherein R1, R2, R3, R4, R5, A and B are as defined in the description. The present invention further relates to a method for preparing the compound, a pharmaceutical composition and a pharmaceutical formulation comprising the compound, and a use of the compound in the manufacture of a medicament for the treatment and/or prevention of infectious diseases and a use for the treatment and/or prevention of infectious diseases.

    摘要翻译: 本发明涉及由通式(I)表示的联芳基杂环取代的恶唑烷酮抗菌剂,其药学上可接受的盐,异构体或前药,其中R 1,R 2,R 3,R 4,R 5,A和B如 说明。 本发明还涉及制备化合物的方法,药物组合物和包含该化合物的药物制剂,以及该化合物在制备用于治疗和/或预防感染性疾病的药物中的用途,以及用于 治疗和/或预防传染病。