IMMUNOMODULATORS
    2.
    发明申请

    公开(公告)号:US20230063238A1

    公开(公告)日:2023-03-02

    申请号:US17791023

    申请日:2020-11-19

    Abstract: In accordance with the present disclosure, macrocyclic compounds of formula (I) have been discovered that bind to PD-L1 and are capable of inhibiting the interaction of PD-L1 with PD-1 and CD80. These macrocyclic compounds exhibit in vitro immunomodulatory efficacy thus making them therapeutic candidates for the treatment of various diseases including cancer and infectious diseases.

    IMMUNOMODULATORS
    3.
    发明申请

    公开(公告)号:US20230022400A1

    公开(公告)日:2023-01-26

    申请号:US17777917

    申请日:2020-11-19

    Abstract: In accordance with the present disclosure, macrocyclic compounds have been discovered that bind to PD-L1 and are capable of inhibiting the interaction of PD-L1 with PD-1 and CD80. These macrocyclic compounds exhibit in vitro immunomodulatory efficacy thus making them therapeutic candidates for the treatment of various diseases including cancer and infectious diseases.

    IMMUNOMODULATORS
    7.
    发明申请

    公开(公告)号:US20230065827A1

    公开(公告)日:2023-03-02

    申请号:US17791027

    申请日:2020-11-19

    Abstract: In accordance with the present disclosure, macrocyclic compounds have been discovered that bind to PD-L1 and are capable of inhibiting the interaction of PD-L1 with PD-1 and CD80. These macrocyclic compounds exhibit in vitro immunomodulatory efficacy thus making them therapeutic candidates for the treatment of various diseases including cancer and infectious diseases.

    MACROCYCLIC MOLECULES AS HCV ENTRY INHIBITORS
    10.
    发明申请
    MACROCYCLIC MOLECULES AS HCV ENTRY INHIBITORS 有权
    作为HCV入侵抑制剂的大分子分子

    公开(公告)号:US20150368251A1

    公开(公告)日:2015-12-24

    申请号:US14765906

    申请日:2014-02-04

    CPC classification number: C07D487/08 A61K31/53 C07D498/08

    Abstract: Compounds of Formula I, including pharmaceutically acceptable salts thereof, are set forth, in addition to compositions and methods of using these compounds. The compounds have activity against hepatitis C virus (HCV) and may be useful in treating those infected with HCV.

    Abstract translation: 除了使用这些化合物的组合物和方法之外,还列举了式I化合物,包括其药学上可接受的盐。 该化合物具有抗丙型肝炎病毒(HCV)的活性,可用于治疗HCV感染者。

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