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DERIVATIVES DERIVATIVES AS AN INHIBITORS OF POLO-SIMILAR KINASE APPLIED IN THE TREATMENT OF CANCER

机译:衍生物作为多径类似激酶的抑制剂在癌症治疗中的应用

摘要

The compounds of formula (I) are inhibitors of Polo-like kinases (PLKs) and are used in the treatment of cell proliferative diseases, where R and R are hydrogen or optionally substituted (C-C) alkyl, (C-C) alkenyl, (C-C) alkynyl or (C — C) cycloalkyl group; R and R 'are independently selected from hydrogen, —CN, hydroxyl, halogen, optionally substituted (C — C) alkyl, (C — C) alkenyl, (C — C) alkynyl or (C — C) cycloalkyl, - NRR or (C — C) alkoxy, where R and R are independently hydrogen or optionally substituted (C — C) alkyl; ring A is an optionally substituted mono- or bicyclic carbocyclic or heterocyclic ring or ring system having up to 12 atoms in the ring; T is a radical of formula R-L-Y, where R is an alpha amino acid or an alpha amino acid ester motif linked to ring A by an R-LY linker as defined in the formula.
机译:式(I)的化合物是Polo样激酶(PLK)的抑制剂,并用于治疗细胞增殖性疾病,其中R和R为氢或任选取代的(CC)烷基,(CC)烯基,(CC)炔基或(CC)环烷基; R和R'独立地选自氢,-CN,羟基,卤素,任选取代的(CC)烷基,(CC)烯基,(CC)炔基或(CC)环烷基,-NRR或(CC)烷氧基,其中R和R独立地为氢或任选取代的(CC)烷基;环A是在环中具有最多12个原子的任选取代的单环或双环碳环或杂环或环系统; T是式R-L-Y的基团,其中R是通过式中定义的R-LY连接基与环A连接的α氨基酸或α氨基酸酯基序。

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