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New G-quadruplex DNA Binders, process for preparation thereof and the use of the same

机译:新的G-四链体DNA结合剂,其制备方法及其用途

摘要

The compositions of the invention are inhibitors of c-myc penoxazone, triazine and pyrazolopyrimidine series relates, more particularly to a pharmaceutical composition for preventing or treating cancer according to a method of manufacturing the same, and this active ingredient. Phenoxazone, triazine series, and pyrazolopyrimidine compounds of the invention may optionally sikimeuroseo stabilize the G-quadruplex structure of c-myc promoter, show the effect of c-myc expression control. This is the development of new anti-cancer DNA target material that exceed the limit of conventional DNA binding anticancer substance, excellent anticancer candidate derived through the optimization of the present invention compounds are c-myc gene is at least wonam induced lung is expressed, result cancer , breast cancer, bladder cancer, can be developed as an anticancer agent for various cancers such as leukemia and is expected to be used in cancer treatment. ;
机译:本发明的组合物是c-myc戊恶唑酮,三嗪和吡唑并嘧啶系列的抑制剂,更具体地涉及根据其制备方法用于预防或治疗癌症的药物组合物,以及该活性成分。本发明的苯并恶唑酮,三嗪系列和吡唑并嘧啶化合物可任选地sikimeuroseo稳定c-myc启动子的G-四链体结构,显示出控制c-myc表达的作用。这是一种新的抗癌DNA靶标材料的开发,该靶标材料超过了常规DNA结合抗癌物质的极限,通过优化本发明化合物衍生的优秀抗癌候选物是c-myc基因,至少表达了wonam诱导的肺,结果癌症,乳腺癌,膀胱癌可以发展为多种癌症(例如白血病)的抗癌药,并有望用于癌症治疗。 ;

著录项

  • 公开/公告号KR101455452B1

    专利类型

  • 公开/公告日2014-10-31

    原文格式PDF

  • 申请/专利权人

    申请/专利号KR20120055692

  • 发明设计人 박현주;한수진;채정현;강현진;

    申请日2012-05-24

  • 分类号C07D265/38;C07D403/12;A61K31/538;A61P35/00;

  • 国家 KR

  • 入库时间 2022-08-21 15:39:51

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