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15 条记录 (耗时 0.02 秒)

    Sodium Channel Blockers, Preparation Method Thereof and Use Thereof
    11.
    发明申请
    Sodium Channel Blockers, Preparation Method Thereof and Use Thereof 有权
    钠通道阻滞剂及其制备方法及用途

    公开(公告)号：US20150336944A1

    公开(公告)日：2015-11-26

    申请号：US14435473

    申请日：2013-10-15

    申请人： DAEWOONG PHARMACEUTICAL CO., LTD.

    发明人： Ha Young Kim ,  In Woo Kim ,  Sun Ah Jun ,  Yun Soo Na ,  Hyung Geun Lee ,  Min Jae Cho ,  Jun Hee Lee ,  Hyo Shin Kim ,  Yun Soo Yoon ,  Kyung Ha Chung ,  Ji Duck Kim

    IPC分类号： C07D417/12 ,  C07D417/14

    CPC分类号： C07D417/12 ,  C07D417/14

    摘要： The present invention relates to a compound having a blocking effect against sodium ion channels, particularly Nav1.7, a preparation method thereof and the use thereof. A compound represented by formula 1 according to the invention, or a pharmaceutically acceptable salt, hydrate, solvate or isomer thereof may be effectively used for the prevention or treatment of pain, for example, acute pain, chronic pain, neuropathic pain, post-surgery pain, migraine, arthralgia, neuropathy, nerve injury, diabetic neuropathy, neuropathic disease, epilepsy, arrhythmia, myotonia, ataxia, multiple sclerosis, irritable bowel syndrome, urinary incontinence, visceral pain, depression, erythromelalgia, or paroxysmal extreme pain disorder (PEPD).

    摘要翻译： 本发明涉及对钠离子通道具有阻塞作用的化合物，特别涉及Nav1.7，其制备方法及其应用。 根据本发明的由式1表示的化合物或其药学上可接受的盐，水合物，溶剂合物或异构体可以有效地用于预防或治疗疼痛，例如急性疼痛，慢性疼痛，神经性疼痛，手术后 疼痛，偏头痛，关节痛，神经病变，神经损伤，糖尿病性神经病变，神经病变，癫痫，心律失常，肌强直，共济失调，多发性硬化症，肠易激综合征，尿失禁，内脏痛，抑郁症，红斑性疼痛或阵发性极度疼痛障碍（PEPD） 。

    Sodium channel blockers, preparation method thereof and use thereof
    13.
    发明授权
    Sodium channel blockers, preparation method thereof and use thereof 有权
    钠通道阻滞剂及其制备方法及用途

    公开(公告)号：US09376429B2

    公开(公告)日：2016-06-28

    申请号：US14435473

    申请日：2013-10-15

    申请人： Daewoong Pharmaceutical Co., Ltd.

    发明人： Ha Young Kim ,  In Woo Kim ,  Sun Ah Jun ,  Yun Soo Na ,  Hyung Geun Lee ,  Min Jae Cho ,  Jun Hee Lee ,  Hyo Shin Kim ,  Yun Soo Yoon ,  Kyung Ha Chung ,  Ji Duck Kim

    IPC分类号： C07D417/12 ,  C07D417/14

    CPC分类号： C07D417/12 ,  C07D417/14

    摘要： The present invention relates to a compound having a blocking effect against sodium ion channels, particularly Nav1.7, a preparation method thereof and the use thereof. A compound represented by formula 1 according to the invention, or a pharmaceutically acceptable salt, hydrate, solvate or isomer thereof may be effectively used for the prevention or treatment of pain, for example, acute pain, chronic pain, neuropathic pain, post-surgery pain, migraine, arthralgia, neuropathy, nerve injury, diabetic neuropathy, neuropathic disease, epilepsy, arrhythmia, myotonia, ataxia, multiple sclerosis, irritable bowel syndrome, urinary incontinence, visceral pain, depression, erythromelalgia, or paroxysmal extreme pain disorder (PEPD).

    摘要翻译： 本发明涉及对钠离子通道具有阻塞作用的化合物，特别涉及Nav1.7，其制备方法及其应用。 根据本发明的由式1表示的化合物或其药学上可接受的盐，水合物，溶剂合物或异构体可以有效地用于预防或治疗疼痛，例如急性疼痛，慢性疼痛，神经性疼痛，手术后 疼痛，偏头痛，关节痛，神经病变，神经损伤，糖尿病性神经病变，神经病变，癫痫，心律失常，肌强直，共济失调，多发性硬化症，肠易激综合征，尿失禁，内脏痛，抑郁症，红斑性疼痛或阵发性极度疼痛障碍（PEPD） 。