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High Throughput Screening Method of Binding Inhibitor between Caspase3 and xAIP and Binding Inhibitor Screened Thereby

机译:高通量筛选Caspase3与xAIP结合抑制剂的方法及其结合抑制剂

摘要

The present invention relates to an ultrafast screening method of caspase3 and xIAP binding inhibitors and to chromomycin A3 screened by the method, and more specifically, to detecting an interaction between caspase3 and xIAP. Reacting a caspase3 or xIAP with a candidate substance that inhibits the binding between caspase3 and xIAP on a biochip, and selecting a candidate substance that inhibits the binding between caspase3 and xIAP as an anticancer substance; and It relates to an inhibitor of binding between caspase3 and xIAP screened by the above method.;According to the present invention, it is possible to develop a target-oriented anticancer agent targeting the apoptosis-related proteins caspase3 and xIAP, which can be applied to customized medicines and concurrent therapies, and using the present invention, screened glycoside antibiotics Chromomycin may be used as a therapeutic agent for hematologic and solid cancers because of its inhibitory activity against the apoptosis-related proteins caspase3 and xIAP.;Apoptosis, glycoside antibiotics, ultrafast screening methods
机译:本发明涉及caspase3和xIAP结合抑制剂的超快筛选方法,并涉及通过该方法筛选的嗜霉素A3,更具体地说,涉及检测caspase3和xIAP之间的相互作用。使caspase3或xIAP与抑制生物芯片上caspase3与xIAP结合的候选物质反应,并选择抑制caspase3与xIAP结合的候选物质作为抗癌物质;通过上述方法筛选的caspase3与xIAP结合的抑制剂。根据本发明,有可能开发针对凋亡相关蛋白caspase3和xIAP的靶向性抗癌剂,并可以应用。针对定制药物和并行疗法,并使用本发明,筛选出的糖苷抗生素因其对凋亡相关蛋白caspase3和xIAP的抑制活性,可被用作血液和实体癌的治疗剂;细胞凋亡,糖苷抗生素,超快速筛选方法

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