FILAMIN A BINDING ANTI-INFLAMMATORY AND ANALGESIC
    2.
    发明申请
    FILAMIN A BINDING ANTI-INFLAMMATORY AND ANALGESIC 有权
    菲林蛋白结合抗炎和毒理学

    公开(公告)号:US20140113895A1

    公开(公告)日:2014-04-24

    申请号:US14137374

    申请日:2013-12-20

    摘要: A compound or its pharmaceutically acceptable salt, optionally including both individual enantiomeric forms, a racemate, diastereomers and mixtures thereof, composition and method are disclosed that can provide analgesia and reduce inflammation. A contemplated compound has a structure that corresponds to Formula A, wherein the R group substituents, d, e, f, k, n, m, D, E, F, K, G, P, Q, W, and Z are defined within.

    摘要翻译: 公开了可以提供止痛和减轻炎症的化合物或其药学上可接受的盐,任选地包括单独的对映体形式,外消旋物,非对映异构体及其混合物。 考虑的化合物具有对应于式A的结构,其中R基团取代基d,e,f,k,n,m,D,E,F,K,G,P,Q,W和Z被定义 中。

    NOVEL ANALGESIC THAT BINDS FILAMIN A
    6.
    发明申请
    NOVEL ANALGESIC THAT BINDS FILAMIN A 审中-公开
    菲律宾蛋白A的新型药物

    公开(公告)号:US20100280061A1

    公开(公告)日:2010-11-04

    申请号:US12435355

    申请日:2009-05-04

    IPC分类号: A61K31/4355 A61P29/00

    CPC分类号: A61K31/4355

    摘要: A compound, composition and method are disclosed that can bind to FLNA and provide analgesia. A contemplated compound has a structure that corresponds to Formula I, wherein R1 and R2 are substituents on W that is a ring structure, R3 and R4 are substituents on the depicted nitrogen atom, m, n and the dotted lines are all defined within.

    摘要翻译: 公开了可以结合FLNA并提供镇痛的化合物,组合物和方法。 考虑的化合物具有对应于式I的结构,其中R 1和R 2是作为环结构的W上的取代基,R 3和R 4是所示氮原子上的取代基,m,n,虚线全部定义。

    Filamin A binding anti-inflammatory and analgesic
    10.
    发明授权
    Filamin A binding anti-inflammatory and analgesic 有权
    Filamin A结合消炎止痛药

    公开(公告)号:US08614324B2

    公开(公告)日:2013-12-24

    申请号:US12719624

    申请日:2010-03-08

    IPC分类号: C07D491/10

    摘要: A compound or its pharmaceutically acceptable salt, optionally including both individual enantiomeric forms, a racemate, diastereomers and mixtures thereof, composition and method are disclosed that can provide analgesia and reduce inflammation. A contemplated compound has a structure that corresponds to Formula A, wherein the R group substituents, d, e, f, k, n, m, D, E, F, K, G, P, Q, W, and Z are defined within.

    摘要翻译: 公开了可以提供止痛和减轻炎症的化合物或其药学上可接受的盐,任选地包括单独的对映体形式,外消旋物,非对映异构体及其混合物。 考虑的化合物具有对应于式A的结构,其中R基团取代基d,e,f,k,n,m,D,E,F,K,G,P,Q,W和Z被定义 中。