会员体验
专利管家(专利管理)
工作空间(专利管理)
风险监控(情报监控)
数据分析(专利分析)
侵权分析(诉讼无效)
联系我们
交流群
官方交流:
QQ群: 891211   
微信请扫码    >>>
现在联系顾问~
热词
    • 7. 发明申请
    • METHODS TO IDENTIFY COMPOUNDS USEFUL FOR THE TREATMENT OF PROLIFERATIVE AND DIFFERENTIATIVE DISORDERS
    • 识别化合物用于治疗增殖性和分化型疾病的方法
    • WO2006113251A2
    • 2006-10-26
    • PCT/US2006013576
    • 2006-04-11
    • UNIV NEW YORKCELGENE CORPPAGANO MICHELEMERCURIO FRANKXIE WEILINLOPEZ-GIRONA ANTONIAPESCHIAROLI ANGELO
    • PAGANO MICHELEMERCURIO FRANKXIE WEILINLOPEZ-GIRONA ANTONIAPESCHIAROLI ANGELO
    • G01N33/50
    • G01N33/5023A61K31/7088A61K38/02A61K38/1709A61K39/3955G01N33/573G01N33/574G01N2333/4703G01N2333/9015G01N2500/00G01N2500/04
    • The present invention relates to the discovery, identification and characterization of nucleotide sequences that encode novel substrate-targeting subunits of ubiquitin ligases. The invention encompasses nucleotides encoding novel substrate-targeting subunits of ubiquitin ligases: FBPl, FBP2, FBP3, FBP4, FBP5, FBP6, FBP7, FBP8, FBP9, FBPlO, FBPI l, FBP12, FBP13, FBP14, FBP15, FBP16, FBP17, FBP18, FBP19, FBP20, FBP21, FBP22, FBP23, FBP24, and FBP25, transgenic mice, knock-out mice, host-cell expression systems and proteins encoded by the nucleotides of the novel substrate-targeting subunits. The present invention relates to screening assays that use novel and known substrate- targeting subunits of ubiquitin ligases to identify potential therapeutic agents such as small molecules, compounds or derivatives and analogues of the novel and known ubiquitin ligases which modulate activity of the novel and known ubiquitin ligases for the treatment of proliferative and differentiative disorders, such as cancer, major opportunistic infections, immune disorders, certain cardiovascular diseases, and inflammatory disorders. The invention further encompasses therapeutic protocols and pharmaceutical compositions designed to target ubiquitin ligases and their substrates for the treatment of proliferative and differentiative disorders.
    • 本发明涉及编码泛素连接酶的新的底物靶向亚基的核苷酸序列的发现,鉴定和表征。 本发明包括编码泛素连接酶的新型底物靶向亚基的核苷酸:FBP1,FBP2,FBP3,FBP4,FBP5,FBP6,FBP7,FBP8,FBP9,FBP10,FBPI1,FBP12,FBP13,FBP14,FBP15,FBP16,FBP17,FBP18 ,FBP19,FBP20,FBP21,FBP22,FBP23,FBP24和FBP25,转基因小鼠,敲除小鼠,宿主细胞表达系统和由新型底物靶向亚基的核苷酸编码的蛋白质。 本发明涉及使用泛素连接酶的新颖且已知的底物靶向亚基的筛选测定法,以鉴定潜在的治疗剂,例如调节新型和已知的泛素的活性的新型和已知的泛素连接酶的小分子,化合物或衍生物和类似物 用于治疗增殖性和分化性疾病如癌症,主要机会性感染,免疫疾病,某些心血管疾病和炎症性疾病的连接酶。 本发明还包括设计用于靶向泛素连接酶及其底物以治疗增殖性和分化性疾病的治疗方案和药物组合物。