首页> 外国专利> Compounds derived from carboxylic acid substituted carbamoyl - hidroisoquinolinas, antiapoptotic Proteins BCL XL inhibitors; Pharmaceutical Composition and method of treatment for breast cancer, cervical cancer, colorectal cancer, Hepatocellular cancer, esophagus cancer, Ucemias, myelomas, among others.

Compounds derived from carboxylic acid substituted carbamoyl - hidroisoquinolinas, antiapoptotic Proteins BCL XL inhibitors; Pharmaceutical Composition and method of treatment for breast cancer, cervical cancer, colorectal cancer, Hepatocellular cancer, esophagus cancer, Ucemias, myelomas, among others.

机译:衍生自羧酸取代的氨基甲酰基-hidroisoquinolinas的化合物,抗凋亡蛋白BCL XL抑制剂;用于乳腺癌,子宫颈癌,结肠直肠癌,肝细胞癌,食道癌,尿毒症,骨髓瘤等的药物组合物和治疗方法。

摘要

Disclosed are compounds of formula (I) which inhibit the activity of anti-apoptotic Bcl-xL proteins, compositions containing the compounds and methods of treating diseases during which Bcl-xL proteins are expressed, eg cancer. X is heteroaryl; Y1 is phenylene or heteroarylene; L1 is a linker; Y2 is cycloalkyi, cycloalkenyl, heterocycloalkyl or heterocycloalkenyl; Z1 is C(0)OR9, C(O)NR10R11, C(0)R11, NR10C(O)R11, etc.
机译:公开了抑制抗凋亡Bcl-xL蛋白活性的式(I)化合物,包含该化合物的组合物和治疗表达Bcl-xL蛋白的疾病例如癌症的方法。 X是杂芳基; Y1为亚苯基或亚杂芳基; L1是链接器; Y 2是环烷基,环烯基,杂环烷基或杂环烯基; Z1是C(0)OR9,C(O)NR10R11,C(0)R11,NR10C(O)R11等。

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