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Interaction with inhibitors of kinase mitogen activated protein kinase (MNK) and Methods related thereto

机译:与激酶促分裂原活化蛋白激酶(MNK)抑制剂的相互作用及其相关方法

摘要

Relates to compounds of formula (i) where W1 and W2 are o, s or N - oru00b4; ru00b4 is lower alkyl; and is N (R5) -, - O -, among others; r1 is H, Lower alkyl, among others; n is 1, 2 or 3; R2 and R3 are H, alkyl, or R2 and R3 with C form a cycloalkyl or heterociclilo R4A r4b are h; and Halogen, R5 is H, among others;Cyano or lower alkyl or R5 and R8 with Atoms that are United to form a heterociclilo condensate; R6, R7 and R8 are h, Hydroxy, among others. It is a Preferred compound: 2 - (6 - [4 - aminopirimidin - il) amino] - 5 - Chloro - 1 - methyl - spiro [2H - imidazo [1,5-a] pyridin-3 3,4u00b4 piperidin] - - - 1.5 - dione; among others. It also relates to a Pharmaceutical composition.These compounds inhibit the kinase mitogen activated protein kinase Interacting Protein (MNK) being useful in the treatment of diseases such as cancer
机译:涉及式(i)的化合物,其中W 1和W 2为o,s或N-或r u00b4是低级烷基;并且是N(R5)-,-O-等。 r1是H,低级烷基等。 n为1、2或3; R2和R3为H,烷基,或R2和R3与C形成环烷基或杂环基R4A,r4b为h;卤素,R 5是H,等等;氰基或低级烷基,或R 5和R 8与与原子结合形成杂环缩合物的原子; R 6,R 7和R 8是h,羟基等。它是优选的化合物:2-(6- [4--氨基嘧啶-il)氨基]-5-氯-1-甲基-螺[2H-咪唑[1,5-a]吡啶-3-3,4 u4b4 ]---1.5-二酮;其中。本发明还涉及药物组合物。这些化合物抑制激酶促分裂原活化蛋白激酶激酶相互作用蛋白(MNK),其可用于治疗诸如癌症的疾病。

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