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ISOQUINOLIN-1 (2H) -ONE DERIVATIVES AS PARP-I INHIBITORS

机译:异喹诺酮1(2H)-一种衍生物作为PARP-I抑制剂

摘要

isoquinolin-1 (2h) -one derivatives as parp-i inhibitors the invention relates to substituted isoquinolin-1 (2h) -one derivatives that selectively inhibit the polypolymer activity (adp-ribose) parp-1 over In addition to poly polymerase (adp-ribose) parp-2, the compounds of the invention are therefore useful in the treatment of diseases such as cancer, cardiovascular diseases, damage to the nervous system and various forms of inflammation. the invention also relates to methods for preparing such compounds, pharmaceutical compositions comprising these compounds, and methods of treating diseases using pharmaceutical compositions comprising these compounds. a screening method for the identification of compounds capable of binding to various parp proteins, thus the evidence used in such a method, are also objects of the invention.
机译:作为parp-i抑制剂的异喹啉-1(2h)-1衍生物本发明涉及取代的异喹啉-1(2h)-1衍生物,其选择性抑制除聚合酶(adp因此,本发明的化合物可用于治疗疾病,例如癌症,心血管疾病,神经系统损害和各种形式的炎症。本发明还涉及制备此类化合物的方法,包含这些化合物的药物组合物以及使用包含这些化合物的药物组合物治疗疾病的方法。用于鉴定能够结合各种parp蛋白的化合物的筛选方法,因此在这种方法中使用的证据也是本发明的目的。

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