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首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Structural insights of oxindole based kinase inhibitors as anticancer agents: Recent advances
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Structural insights of oxindole based kinase inhibitors as anticancer agents: Recent advances

机译:基于氧吲哚基激酶抑制剂作为抗癌剂的结构见解:最近的进展

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摘要

Small-molecule kinase inhibitors are being continuously explored as new anticancer therapeutics. Kinases are the phosphorylating enzymes which regulate numerous cellular functions such as proliferation, differentiation, migration, metabolism, and angiogenesis by activating several signalling pathways. Kinases have also been frequently found to be deregulated and overexpressed in cancerous tissues. Therefore, modulating the kinase activity by employing small molecules has emerged as a strategic approach for cancer treatment. On the other hand, oxindole motifs have surfaced as privileged scaffolds with significant multi-kinase inhibitory activity. The present review summarises recent advances in the development of oxindole based kinase inhibitors. The role of distinguished structural frameworks of oxindoles, such as 3-alkenyl oxindoles, spirooxindoles, 3-iminooxindoles and similar hydrazone derivatives have been described based on their kinase inhibition potential. Furthermore, the design strategies, mechanism of actions, structure activity relationships (SARs) and their mode of interaction with target protein have been critically highlighted. (C) 2021 Elsevier Masson SAS. All rights reserved.
机译:小分子激酶抑制剂作为一种新的抗癌药物正在不断被探索。激酶是一种磷酸化酶,通过激活多种信号通路来调节多种细胞功能,如增殖、分化、迁移、代谢和血管生成。激酶也经常被发现在癌组织中被解除调控和过度表达。因此,利用小分子调节激酶活性已成为癌症治疗的一种战略方法。另一方面,oxindole基序已作为具有显著多激酶抑制活性的特权支架出现。本文综述了基于奥克西多尔的激酶抑制剂的最新进展。基于其激酶抑制潜力,已经描述了奥辛多尔的独特结构框架的作用,例如3-烯基奥辛多尔、螺环辛多尔、3-亚氨基辛多尔和类似的腙衍生物。此外,设计策略、作用机制、结构-活性关系(SARs)及其与靶蛋白的相互作用模式也得到了严格的强调。(c)2021爱思唯尔马松SAS。版权所有。

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