7-BETA-ALKYL ANALOGS OF ORVINOLS
    1.
    发明申请

    公开(公告)号:US20170204113A1

    公开(公告)日:2017-07-20

    申请号:US15107025

    申请日:2014-12-23

    发明人: Laykea TAFESSE

    IPC分类号: C07D491/08

    CPC分类号: C07D491/08 C07D489/12

    摘要: The application is directed to compounds of Formula (I) and pharmaceutically acceptable salts and solvates thereof, wherein R1, R1a, R1b, R1c, X, Y, Z, G, O, W1 and W2 are defined as set forth in the specification. The invention is also directed to use of compounds of Formula (I), and the pharmaceutically acceptable salts and solvates thereof, to treat disorders responsive to the modulation of one or more opioid receptors, or as synthetic intermediates. Certain compounds of the present invention are especially useful for treating pain.

    OXAZOLINE PSEUDODIMERS, PHARMACEUTICAL COMPOSITIONS AND THE USE THEREOF

    公开(公告)号:US20190144400A1

    公开(公告)日:2019-05-16

    申请号:US16098494

    申请日:2017-05-04

    IPC分类号: C07D263/28 A61P25/04

    摘要: The present disclosure is directed to oxazoline mono- and hetero-pseudodimer compounds, such as compounds of Formula (I) or pharmaceutically acceptable salts or solvates thereof: These compounds are useful for treating pain. The present disclosure also relates to pharmaceutical compositions comprising a pharmaceutically acceptable carrier and a therapeutically effective amount of a compound of Formula (I) or (II) or a pharmaceutically acceptable salt or solvate thereof.

    Spirocyclic Morphinans and Their Use
    7.
    发明申请
    Spirocyclic Morphinans and Their Use 有权
    螺环状吗啡及其用途

    公开(公告)号:US20140179724A1

    公开(公告)日:2014-06-26

    申请号:US14105710

    申请日:2013-12-13

    IPC分类号: C07D471/20

    CPC分类号: C07D471/10 C07D471/20

    摘要: The application is directed to compounds of Formula I′-A especially to compounds of Formula I-A and pharmaceutically acceptable salts and solvates thereof, wherein R1a-R5a, Y, Z are defined as set forth in the specification. The invention is also directed to use of compounds of Formula I′-A, and especially compounds of Formula I-A, to treat disorders responsive to the modulation of one or more opioid receptors, or as synthetic intermediates. Certain compounds of the present invention are especially useful for treating pain.

    摘要翻译: 本发明涉及式I'-A化合物,特别是式I-A化合物及其药学上可接受的盐和溶剂合物,其中R1a-R5a,Y,Z如说明书所述定义。 本发明还涉及使用式I'-A化合物,特别是式I-A的化合物来治疗对一种或多种阿片样物质受体或作为合成中间体的调节作用的病症。 本发明的某些化合物特别适用于治疗疼痛。

    Pyridonemorphinan Analogs and Biological Activity on Opioid Receptors
    9.
    发明申请
    Pyridonemorphinan Analogs and Biological Activity on Opioid Receptors 有权
    吡啶并吗啡类似物和对阿片受体的生物活性

    公开(公告)号:US20140187549A1

    公开(公告)日:2014-07-03

    申请号:US14105733

    申请日:2013-12-13

    发明人: Laykea TAFESSE

    IPC分类号: C07D471/22

    摘要: The application is directed to compounds of Formula I-A and pharmaceutically acceptable salts and solvates thereof, wherein , R1a, R3a, R4, Y and Za are defined as set forth in the specification. The invention is also directed to use of compounds of Formula I-A to treat disorders responsive to the modulation of one or more opioid receptors, or as synthetic intermediates. Certain compounds of the present invention are especially useful for treating pain.

    摘要翻译: 本申请涉及式I-A化合物及其药学上可接受的盐和溶剂化物,其中R1a,R3a,R4,Y和Za如本说明书所述定义。 本发明还涉及使用式I-A的化合物来治疗对一种或多种阿片样物质受体的调节或作为合成中间体的病症。 本发明的某些化合物特别适用于治疗疼痛。