DIAGNOSTIC METHOD FOR DETECTING A GABA(A) RELATED AUTOIMMUNE DISEASE AND RELATED SUBJECT-MATTER
    5.
    发明申请
    DIAGNOSTIC METHOD FOR DETECTING A GABA(A) RELATED AUTOIMMUNE DISEASE AND RELATED SUBJECT-MATTER 审中-公开
    用于检测GABA(A)相关自身免疫疾病和相关主题的诊断方法

    公开(公告)号:US20160326227A1

    公开(公告)日:2016-11-10

    申请号:US15023131

    申请日:2014-10-16

    发明人: Josep Dalmau

    摘要: The present invention provides a use of a GABA(A)R, GABA(A)R fragment, or homolog thereof or a cell expressing the GABA(A)R, GABA(A)R fragment, or homolog thereof for the prognosis, diagnosis or treatment of an autoimmune disease in a subject, methods of prognosticating, diagnosing or treating an autoimmune disease, an autoantibody binding to a GABA(A)R, GABA(A)R fragment, or homolog thereof, a method for isolating an antibody binding to a GABA(A)R, GABA(A)R fragment, or homolog thereof, and a test kit, pharmaceutical composition and medical or diagnostic device comprising a GABA(A)R, GABA(A)R fragment, or homolog thereof.

    摘要翻译: 本发明提供了GABA(A)R,GABA(A)R片段或其同源物或表达GABA(A)R,GABA(A)R片段或其同源物的细胞用于预后,诊断的用途 或治疗受试者中的自身免疫疾病,预后,诊断或治疗自身免疫疾病的方法,与GABA(A)R,GABA(A)R片段或其同系物结合的自身抗体,分离抗体结合的方法 (A)R,GABA(A)R片段或其同源物,以及包含GABA(A)R,GABA(A)R片段或其同系物的测试试剂盒,药物组合物和医学或诊断装置。

    MU OPIOID RECEPTOR AGONIST ANALOGS OF THE ENDOMORPHINS
    7.
    发明申请
    MU OPIOID RECEPTOR AGONIST ANALOGS OF THE ENDOMORPHINS 审中-公开
    内啡肽的阿片受体激动剂类似物

    公开(公告)号:US20160176930A1

    公开(公告)日:2016-06-23

    申请号:US14974249

    申请日:2015-12-18

    IPC分类号: C07K7/64

    摘要: The invention relates to cyclic peptide agonists that bind to the mu (morphine) opioid receptor and their use in the treatment of acute and/or chronic pain. Embodiments of the invention are directed to cyclic pentapeptide and hexapeptide analogs of endomorphin that have (i) a carboxy-terminal extension with an amidated amino acid and (ii) a D-amino acid substitution in position 2. These peptide analogs exhibit decreased tolerance relative to morphine, increased solubility compared to similar tetrapeptide analogs, while maintaining favorable or improved therapeutic ratios of analgesia to side effects.

    摘要翻译: 本发明涉及结合mu(吗啡)阿片受体的环肽激动剂及其在治疗急性和/或慢性疼痛中的用途。 本发明的实施方案涉及内啡肽的环状五肽和六肽类似物,其具有(i)具有酰胺化氨基酸的羧基末端延伸和(ii)位置2的D-氨基酸取代。这些肽类似物显示出降低的耐受性相对 吗啡,与类似的四肽类似物相比增加溶解度,同时保持镇痛与副作用的有利或改善的治疗比。