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Artemisinin-derived hybrids and their anticancer activity

机译:青蒿素衍生的杂种及其抗癌活动

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摘要

The emergence of drug-resistance and the low specificity of anticancer agents are the major challenges in the treatment of cancer and can result in many side effects, creating an urgent demand to develop novel anticancer agents. Artemisinin-derived compounds, bearing a peroxide-containing sesquiterpene lactone moiety, could form free radicals with high reactivity and possess diverse pharmaceutical properties including in vitro and in vivo anticancer activity besides their typical antimalarial activity. Hybrid molecules have the potential to improve the specificity and overcome the drug resistance, therefore hybridization of artemisinin skeleton with other anticancer pharmacophores may provide novel anticancer candidates with high specificity and great potency against drug-resistant cancers. The review outlines the recent advances of artemisinin-derived hybrids as potential anticancer agents, and the structure-activity relationships are also discussed to provide an insight for rational designs of novel hybrids with high activity. (C) 2020 Elsevier Masson SAS. All rights reserved.
机译:抗药性和抗癌剂的低特异性的出现是治疗癌症的主要挑战,可能导致许多副作用,促进开发新型抗癌剂的迫切需求。含有过氧化物的倍二萜内酯部分的青蒿素衍生的化合物可以形成具有高反应性的自由基,并且除了其典型的抗疟活动之外,具有多种药物性能,包括体外和体内抗癌活性。杂化分子具有改善特异性和克服耐药性的潜力,因此与其他抗癌药物的野生素骨骼骨架的杂交可以提供具有高特异性和耐药性癌症的高特异性和良好效力的新抗癌候选者。审查概述了青蒿素衍生的杂种作为潜在抗癌剂的最新进展,并且还讨论了结构 - 活动关系,为高活动的新型杂种的合理设计提供了洞察力。 (c)2020 Elsevier Masson SAS。版权所有。

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