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1,3,5-三嗪-唑杂化物及其抗癌活性。

1,3,5-Triazine-azole Hybrids and their Anticancer Activity.

作者信息

Guo Hua, Diao Quan-Ping

机构信息

School of Chemistry and Life Science, Anshan Normal University, Anshan, Liaoning, China.

出版信息

Curr Top Med Chem. 2020;20(16):1481-1492. doi: 10.2174/1568026620666200310122741.

Abstract

1,3,5-Triazine and azole can interact with various therapeutic targets, and their derivatives possess promising in vitro and in vivo anticancer activity. Hybrid molecules have the potential to enhance efficiency, overcome drug resistance and reduce side effects, and many hybrid molecules are under different phases of clinical trials, so hybridization of 1,3,5-triazine with azole may provide valuable therapeutic intervention for the treatment of cancer. Substantial efforts have been made to develop azole-containing 1,3,5-triazine hybrids as novel anticancer agents, and some of them exhibited excellent activity. This review emphasizes azole-containing 1,3,5-triazine hybrids with potential anticancer activity, and the structure-activity relationships as well as the mechanisms of action are also discussed to provide comprehensive and target-oriented information for the development of this kind of anticancer drugs.

摘要

1,3,5-三嗪和唑类可与多种治疗靶点相互作用,其衍生物具有良好的体外和体内抗癌活性。杂化分子有提高疗效、克服耐药性和减少副作用的潜力,许多杂化分子正处于不同阶段的临床试验中,因此1,3,5-三嗪与唑类的杂化可能为癌症治疗提供有价值的治疗干预。人们已付出巨大努力开发含唑类的1,3,5-三嗪杂化物作为新型抗癌剂,其中一些表现出优异的活性。本综述着重介绍具有潜在抗癌活性的含唑类1,3,5-三嗪杂化物,并讨论其构效关系及作用机制,为这类抗癌药物的开发提供全面且有针对性的信息。

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