首页> 外国专利> Use of cyclophilin D or creatine kinase for inhibiting apoptosis, useful for treating e.g. cardiac infarct and in drug screening, also use of their inhibitors for treating tumors

Use of cyclophilin D or creatine kinase for inhibiting apoptosis, useful for treating e.g. cardiac infarct and in drug screening, also use of their inhibitors for treating tumors

机译:亲环蛋白D或肌酸激酶用于抑制细胞凋亡的用途,可用于治疗例如心脏梗塞和药物筛查中,还使用其抑制剂治疗肿瘤

摘要

Use of cyclophilin D (I) and/or creatine kinase (II), or their biologically active fragments or derivatives; nucleic acids that encode them, and their activators (collectively (A)), for inhibiting apoptotic processes that are not associated with ANT-1 (adenine nucleotide translocase-1). Independent claims are also included for the following: (1) pharmaceutical composition containing (i) fusion protein of (I) or (II) with a heterologous protein, (ii) a derivative of (I) without chaperone function, (iii) a derivative of (II) without enzymatic activity and (iv) nucleic acid encoding (i)-(iii); (2) use of an inhibitor of (I) or (II) for inhibiting hyperproliferation and/or autoimmune processes; (3) transgenic non-human organism, or eukaryotic cell, that under- or over-expresses (I) and/or (II); and (4) use of an effector molecule directed against the amino acid regions 1-17, 67-107 and/or 151-170 regions of ANT-1 for modulating ANT-1 associated apoptosis. ACTIVITY : Cardiant; Cerebroprotective; Vasotropic; Nootropic; Neuroprotective; Antiparkinsonian; Ophthalmological; Hepatotropic; Antianemic; Anti-AIDS; Cytostatic; Immunosuppressive; Nephrotropic; Virucide. No details of tests for these activities are given. MECHANISM OF ACTION : (A) inhibit apoptotic processes associated with: activation of permeability transition pores; caspase 8, tBid and/or bax; inhibitors of tumor necrosis factor/cycloheximide; UV light and/or diarsenic trioxide; cytostatics or hypoxia. No biological data given.
机译:亲环蛋白D(I)和/或肌酸激酶(II)或其生物活性片段或衍生物的用途;编码它们的核酸及其激活剂(统称为(A)),用于抑制与ANT-1不相关的凋亡过程(腺嘌呤核苷酸translocase-1)。还包括以下方面的独立权利要求:(1)药物组合物,其包含(i)(I)或(II)与异源蛋白的融合蛋白,(ii)(I)没有伴侣功能的衍生物,(iii)a (II)没有酶活性的衍生物,和(iv)编码(i)-(iii)的核酸; (2)(I)或(II)的抑制剂在抑制过度增殖和/或自身免疫过程中的用途; (3)低于或过量表达(I)和/或(II)的转基因非人类生物或真核细胞; (4)针对ANT-1的氨基酸区域1-17、67-107和/或151-170区域的效应分子在调节ANT-1相关的细胞凋亡中的用途。活动:Cardiant;脑保护变压性促智;具有神经保护作用;反帕金森病;眼科肝抗贫血;抗艾滋病;细胞抑制免疫抑制嗜肾杀病毒剂。没有提供这些活动的测试详细信息。作用机理:(A)抑制与以下过程有关的凋亡过程:渗透性过渡孔的激活;半胱天冬酶8,tBid和/或bax;肿瘤坏死因子/环己酰亚胺抑制剂;紫外线和/或三氧化二砷;细胞抑制剂或缺氧。没有给出生物学数据。

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