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Ferrocene-containing hybrids as potential anticancer agents: Current developments, mechanisms of action and structure-activity relationships.
European Journal of Medicinal Chemistry ( IF 6.0 ) Pub Date : 2020-01-30 , DOI: 10.1016/j.ejmech.2020.112109
Ruo Wang 1 , Huahong Chen 1 , Weitao Yan 1 , Mingwen Zheng 1 , Tesen Zhang 1 , Yaohuan Zhang 1
Affiliation  

Cancer is one of the most fatal threatens to human health throughout the world. The major challenges in the control and eradication of cancers are the continuous emergency of drug-resistant cancer and the low specificity of anticancer agents, creating an urgent need to develop novel anticancer agents. Organometallic compounds especially ferrocene derivatives possess remarkable structural and mechanistic diversity, inherent stability towards air, heat and light, low toxicity, low cost, reversible redox, ligand exchange, and catalytic properties, making them promising drug candidates for cancer therapy. Ferrocifen, a ferrocene-phenol hybrid, has demonstrated promising anticancer properties on drug-resistant cancers. Currently, Ferrocifen is in pre-clinical trial against cancers. Obviously, ferrocene moiety is a useful template for the development of novel anticancer agents. This review will provide an overview of ferrocene-containing hybrids with potential application in the treatment of cancers covering articles published between 2010 and 2020. The mechanisms of action, the critical aspects of design and structure-activity relationships are also discussed.

中文翻译:

含二茂铁的杂化物作为潜在的抗癌药:当前的发展,作用机理和构效关系。

癌症是全世界人类健康最致命的威胁之一。在控制和根除癌症方面的主要挑战是耐药性癌症的持续不断发展和抗癌药特异性低,迫切需要开发新型抗癌药。有机金属化合物,特别是二茂铁衍生物具有显着的结构和机制多样性,对空气,热和光的固有稳定性,低毒性,低成本,可逆氧化还原,配体交换和催化特性,使其成为有望用于癌症治疗的药物。二茂铁-苯酚杂化物Ferrocifen已显示出对耐药性癌症有希望的抗癌特性。目前,Ferrocifen正在进行针对癌症的临床前试验。明显,二茂铁部分是开发新型抗癌剂的有用模板。这篇综述将概述含二茂铁的杂种及其在癌症治疗中的潜在应用,涵盖2010年至2020年之间发表的文章。还讨论了作用机理,设计的关键方面以及构效关系。
更新日期:2020-01-31
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