首页> 外国专利> Compound capable of modulating interaction between the PTB1 domain of FE65 protein and hnRNPL and/or FEBP1 protein, useful to treat neurological disorders including Alzheimer's disease

Compound capable of modulating interaction between the PTB1 domain of FE65 protein and hnRNPL and/or FEBP1 protein, useful to treat neurological disorders including Alzheimer's disease

机译:能够调节FE65蛋白的PTB1结构域与hnRNPL和/或FEBP1蛋白之间相互作用的化合物,可用于治疗包括阿尔茨海默氏病在内的神经系统疾病

摘要

A compound capable of at least partially modulating interactions between hnRNPL (undefined) and/or FEBP1 (undefined) proteins or their homologues and the PTB1 domain of FE65, is new. Independent claims are also included for the following: (i) a 337 amino acid sequence (I) fully defined in the specification or its derivative or fragment; (ii) a polypeptide (II) derived from a 349 amino acid sequence fully defined in the specification having a non-functional effector region; (iii) a nucleic acid encoding the above polypeptides; (iv) a nucleic acid capable of hybridizing with the above nucleic acid or its complement; (v) a vector comprising one of the above nucleic acids; (vi) a disarmed recombinant virus comprising one of the above nucleic acids; (vii) an antibody or its fragment directed against the above polypeptide; (viii) a non-peptide or naturally not exclusively peptide compound susceptible for modulating interaction between hnRNPL and/or FEBP1 proteins or their homologues and the PTB1 domain of FE65; (ix) selecting or characterizing active molecules, comprising selecting for molecules capable of binding to sequence I or II or their fragments; and (x) producing the above peptide compound, comprising culturing a cell containing the above nucleic acid or vector under expression conditions, and recovering the peptide compound product. ACTIVITY : Nootropic; neuroprotective. No supporting data is given. MECHANISM OF ACTION : Modulating protein-protein interactions, particularly to prevent formation of amyloid plaques.
机译:能够至少部分调节hnRNPL(未定义)和/或FEBP1(未定义)蛋白或其同源物与FE65的PTB1域之间相互作用的化合物是新的。还包括以下方面的独立权利要求:(i)说明书中完全定义的337个氨基酸序列(I)或其衍生物或片段; (ii)衍生自说明书中完全定义的349个氨基酸序列的多肽(II),具有非功能性效应子区域; (iii)编码上述多肽的核酸; (iv)能够与上述核酸或其互补序列杂交的核酸; (v)包含上述核酸之一的载体; (vi)解除武装的重组病毒,其包含上述核酸之一; (vii)针对上述多肽的抗体或其片段; (viii)易调节hnRNPL和/或FEBP1蛋白或其同源物与FE65的PTB1域之间相互作用的非肽或天然非排他性肽化合物; (ix)选择或表征活性分子,包括选择能够结合序列I或II或其片段的分子; (x)产生上述肽化合物,包括在表达条件下培养含有上述核酸或载体的细胞,并回收肽化合物产物。活动:促智;具有神经保护作用。没有提供支持数据。作用机理:调节蛋白质-蛋白质相互作用,特别是防止淀粉样斑块的形成。

著录项

  • 公开/公告号FR2804962A1

    专利类型

  • 公开/公告日2001-08-17

    原文格式PDF

  • 申请/专利权人 AVENTIS PHARMA S.A.;

    申请/专利号FR20000001628

  • 发明设计人 MAURY ISABELLE;MERCKEN LUC;FOURNIER ALAIN;

    申请日2000-02-10

  • 分类号C07K14/47;C12N15/12;C12N15/63;C07K16/18;A61K38/17;A61K39/395;A61K48/00;A61P25/28;G01N33/53;

  • 国家 FR

  • 入库时间 2022-08-22 01:07:42

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