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杂环查尔酮类似物作为潜在的抗癌剂。

Heterocyclic chalcone analogues as potential anticancer agents.

机构信息

Institute of Pharmaceutical Sciences, Kurukshetra University, Kurukshetra-136119, India.

出版信息

Anticancer Agents Med Chem. 2013 Mar;13(3):422-32.

Abstract

Chalcones, aromatic ketones and enones acting as the precursor for flavonoids such as Quercetin, are known for their anticancer effects. Although, parent chalcones consist of two aromatic rings joined by a three-carbon α,β-unsaturated carbonyl system, various synthetic compounds possessing heterocyclic rings like pyrazole, indole etc. are well known and proved to be effective anticancer agents. In addition to their use as anticancer agents in cancer cell lines, heterocyclic analogues are reported to be effective even against resistant cell lines. In this connection, we hereby highlight the potential of various heterocyclic chalcone analogues as anticancer agents with a brief summary about therapeutic potential of chalcones, mechanism of anticancer action of various chalcone analogues, and current and future prospects related to the chalcones-derived anticancer research. Furthermore, some key points regarding chalcone analogues have been reviewed by analyzing their medicinal properties.

摘要

查耳酮、芳香酮和烯酮作为黄酮类化合物如槲皮素的前体,具有抗癌作用。尽管母查耳酮由通过一个三碳α,β-不饱和羰基系统连接的两个芳香环组成,但各种具有杂环如吡唑、吲哚等的合成化合物是众所周知的,并被证明是有效的抗癌剂。除了在癌细胞系中用作抗癌剂之外,杂环类似物甚至对耐药细胞系也有效。在这方面,我们在此强调各种杂环查耳酮类似物作为抗癌剂的潜力,并简要总结查耳酮的治疗潜力、各种查耳酮类似物的抗癌作用机制以及与查耳酮衍生的抗癌研究相关的当前和未来前景。此外,通过分析查耳酮类似物的药用特性,对其进行了一些要点回顾。

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