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首页> 外文期刊>Medicinal chemistry >Synthesis of 1,4-disubstituted 1,2,3-triazole Derivatives Using Click Chemistry and their Src Kinase Activities
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Synthesis of 1,4-disubstituted 1,2,3-triazole Derivatives Using Click Chemistry and their Src Kinase Activities

机译:使用咔哒化学及其SRC激酶活动合成1,4-二取代的1,2,3-三唑衍生物

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Background: Tyrosine kinases (TK) are enzymes that catalyze the phosphorylation of tyrosine residues on proteins by the transfer of phosphate moiety of ATP. TK are key regulators of various cell functions, such as cellular growth, proliferation, migration, differentiation, and apoptosis. Src mutations and/or overexpression has been correlated with tumor growth, metastasis, and angiogenesis [4,5]. Thus, the design and the discovery of novel Src kinase inhibitors remains critically important.
机译:背景:酪氨酸激酶(TK)是通过ATP的磷酸盐部分转移催化蛋白质对蛋白质上的酪氨酸残基的磷酸化酶。 TK是各种细胞功能的关键调节因子,例如细胞生长,增殖,迁移,分化和细胞凋亡。 SRC突变和/或过表达与肿瘤生长,转移和血管生成相关[4,5]。 因此,新型SRC激酶抑制剂的设计和发现仍然至关重要。

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