METHODS AND COMPOSITIONS OF P27KIP1 TRANSCRIPTIONAL MODULATORS
    4.
    发明申请
    METHODS AND COMPOSITIONS OF P27KIP1 TRANSCRIPTIONAL MODULATORS 有权
    P27KIP1转录调节因子的方法和组成

    公开(公告)号:US20160030445A1

    公开(公告)日:2016-02-04

    申请号:US14774597

    申请日:2014-03-15

    Abstract: In one aspect, the invention relates to pharmaceutical compositions comprising agents that activate the expression of Atoh1, or pharmaceutically acceptable salts, solvates, or polymorphs thereof; and agents that inhibit the expression of p27Kip1, or pharmaceutically acceptable salts, solvates, or polymorphs thereof, which are useful for inducing the formation of cochlear hair cells; and methods of treating hearing impairments or disorders using the compositions. In one aspect, the invention relates to pharmaceutical compositions comprising β-catenin; and agents that activate the expression of Atoh1, or pharmaceutically acceptable salts, solvates, or polymorphs thereof. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.

    Abstract translation: 一方面,本发明涉及包含活化Atoh1表达的试剂或其药学上可接受的盐,溶剂合物或多晶型物的药物组合物; 以及抑制p27Kip1或其药学上可接受的盐,溶剂合物或多晶型物的表达的试剂,其可用于诱导耳蜗毛细胞的形成; 以及使用该组合物治疗听力障碍或障碍的方法。 一方面,本发明涉及包含β-联蛋白的药物组合物; 以及激活Atoh1表达的药剂,或其药学上可接受的盐,溶剂化物或多晶型物。 该摘要旨在作为用于在特定技术中进行搜索的扫描工具,而不意在限制本发明。

    Methods and compositions of p27KIP1 transcriptional modulators
    7.
    发明授权
    Methods and compositions of p27KIP1 transcriptional modulators 有权
    p27KIP1转录调节剂的方法和组成

    公开(公告)号:US09572815B2

    公开(公告)日:2017-02-21

    申请号:US14774597

    申请日:2014-03-15

    Abstract: In one aspect, the invention relates to pharmaceutical compositions comprising agents that activate the expression of Atoh1, or pharmaceutically acceptable salts, solvates, or polymorphs thereof; and agents that inhibit the expression of p27Kip1, or pharmaceutically acceptable salts, solvates, or polymorphs thereof, which are useful for inducing the formation of cochlear hair cells; and methods of treating hearing impairments or disorders using the compositions. In one aspect, the invention relates to pharmaceutical compositions comprising β-catenin; and agents that activate the expression of Atoh1, or pharmaceutically acceptable salts, solvates, or polymorphs thereof. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.

    Abstract translation: 一方面,本发明涉及包含活化Atoh1表达的试剂或其药学上可接受的盐,溶剂化物或多晶型物的药物组合物; 以及抑制p27Kip1或其药学上可接受的盐,溶剂合物或多晶型物的表达的试剂,其可用于诱导耳蜗毛细胞的形成; 以及使用该组合物治疗听力障碍或障碍的方法。 一方面,本发明涉及包含β-连环蛋白的药物组合物; 以及激活Atoh1表达的药剂,或其药学上可接受的盐,溶剂化物或多晶型物。 该摘要旨在作为用于在特定技术中进行搜索的扫描工具,而不意在限制本发明。

    1,4,5-substituted 1,2,3-triazole analogues as antagonists of the pregnane X receptor

    公开(公告)号:US10947203B2

    公开(公告)日:2021-03-16

    申请号:US16679007

    申请日:2019-11-08

    Abstract: In an aspect, the invention relates to 1,4,5-substituted 1,2,3-triazole and 1,2,4,5-substituted imidazoles having a structure represented by a formula: which are modulators the pregnane X receptor (“PXR”); synthesis methods for making the compounds; pharmaceutical compositions comprising the compounds; and methods of modulating an adverse drug reaction in a mammal using the compounds and pharmaceutical compositions; methods of treatment of a disorder of uncontrolled cellular proliferation, such as a cancer, using the compounds and pharmaceutical compositions; methods of modulating pregnane X receptor activity in a mammal using the compounds and pharmaceutical compositions. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.

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