OLIGOMER-CONTAINING PYRROLIDINE COMPOUNDS
    82.
    发明申请
    OLIGOMER-CONTAINING PYRROLIDINE COMPOUNDS 有权
    含低分子吡咯烷酮化合物

    公开(公告)号:US20140288315A1

    公开(公告)日:2014-09-25

    申请号:US14297149

    申请日:2014-06-05

    IPC分类号: C07D207/27

    摘要: The invention relates to (among other things) oligomer-containing pyrrolidine compounds. A compound of the invention, when administered by any of a number of administration routes, exhibits one or more advantages over corresponding compounds lacking the oligomer.

    摘要翻译: 本发明涉及(尤其是)含低聚物的吡咯烷化合物。 当通过任何多种施用途径给药时,本发明的化合物显示出相对于缺乏寡聚物的相应化合物的一个或多个优点。

    Oligomer-Dantrolene Conjugates and Related Compounds
    83.
    发明申请
    Oligomer-Dantrolene Conjugates and Related Compounds 有权
    低聚异戊二烯共轭物和相关化合物

    公开(公告)号:US20130338204A1

    公开(公告)日:2013-12-19

    申请号:US13971391

    申请日:2013-08-20

    IPC分类号: A61K47/48

    CPC分类号: A61K47/48215 A61K47/60

    摘要: The invention relates to (among other things) oligomer-dantrolene conjugates and related compounds. A conjugate of the invention, when administered by any of a number of administration routes, exhibits advantages over previously administered compounds.

    摘要翻译: 本发明涉及(尤其是)低聚物 - 丹曲林共轭物和相关化合物。 本发明的缀合物当通过任何多种施用途径施用时,显示出优于先前施用的化合物的优点。

    OLIGOMER-PHENOTHIAZINE CONJUGATES
    86.
    发明申请

    公开(公告)号:US20200038517A1

    公开(公告)日:2020-02-06

    申请号:US16599605

    申请日:2019-10-11

    IPC分类号: A61K47/60

    摘要: The invention relates to (among other things) oligomer-phenothiazine conjugates and related compounds. A conjugate of the invention, when administered by any of a number of administration routes, exhibits advantages over un-conjugated phenothiazine compounds.

    OLIGOMER-BETA BLOCKER CONJUGATES
    89.
    发明申请

    公开(公告)号:US20170360948A1

    公开(公告)日:2017-12-21

    申请号:US15690106

    申请日:2017-08-29

    IPC分类号: A61K47/60

    CPC分类号: A61K47/60

    摘要: The invention provides small molecule drugs that are chemically modified by covalent attachment of a water-soluble oligomer. A conjugate of the invention, when administered by any of a number of administration routes, exhibits a different biological membrane crossing rate as compared to the biological membrane crossing rate of the small molecule drug not attached to the water-soluble oligomer.