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Aldehyde group pyridine derivative showing FGFR4 inhibitory activity, its production method and application

机译:醛基吡啶衍生物显示FGFR4抑制活性,其生产方法和应用

摘要

The present invention relates to formylpyridine derivatives having FGFR4 inhibitory activities, a preparation method therefor and use thereof, the formylpyridine derivatives having a structure of formula (I), the definition of each substituent in the formula being as described in the description and claims. The series of compounds of the present invention have very strong inhibitory effects on FGFR4 kinases, have very high selectivity, and can be widely used in the preparation of medicaments for treating cancers, particularly prostate cancer, liver cancer, pancreatic cancer, esophageal cancer, stomach cancer, lung cancer, breast cancer, ovarian cancer, colon cancer, skin cancer, neuroglioblastoma or rhabdomyosarcoma, and prospectively will be further developed to become a new generation of FGFR4 inhibitors.
机译:本发明涉及具有FGFR4抑制活性的甲酰吡啶衍生物,其制备方法及其用途,具有式(I)结构的甲基吡啶衍生物,如说明书和权利要求所述的公式中的每种取代基的定义。 本发明的一系列化合物对FGFR4激酶具有非常强烈的抑制作用,具有非常高的选择性,并且可以广泛用于制备用于治疗癌症的药物,特别是前列腺癌,肝癌,胰腺癌,食道癌,胃癌 癌症,肺癌,乳腺癌,卵巢癌,结肠癌,皮肤癌,神经腺细胞瘤或横纹肌肉瘤,并将进一步发展成为新一代FGFR4抑制剂。

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