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Photochemical Properties and Structure–Activity Relationships of RuII Complexes with Pyridylbenzazole Ligands as Promising Anticancer Agents

机译:吡啶基苯并恶唑配体RuII配合物的光化学性质和构效关系

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摘要

Ruthenium complexes capable of light-triggered cytotoxicity are appealing potential prodrugs for photodynamic therapy (PDT) and photoactivated chemotherapy (PACT). Two groups of Ru(II) polypyridyl complexes with 2-(2-pyridyl)-benzazole ligands were synthesized and investigated for their photochemical properties and anticancer activity to compare strained and unstrained systems that are likely to have different biological mechanisms of action. The structure-activity relationship was focused on the benzazole core bioisosterism and replacement of coligands in Ru(II) complexes. Strained compounds rapidly ejected the 2-(2-pyridyl)-benzazole ligand after light irradiation, and possessed strong toxicity in the HL-60 cell line both under dark and light conditions. In contrast, unstrained Ru(II) complexes were non-toxic in the absence of light, induced cytotoxicity at nanomolar concentrations after light irradiation, and are capable of light-induced DNA damage. The 90−220-fold difference in light and dark IC50 values provides a large potential therapeutic window to allow for selective targeting of cells by exposure to light.
机译:能够光触发细胞毒性的钌配合物是用于光动力疗法(PDT)和光活化化学疗法(PACT)的诱人潜在前药。合成了两组具有2-(2-吡啶基)-苯并唑配体的Ru(II)聚吡啶基配合物,并研究了它们的光化学性质和抗癌活性,以比较可能具有不同生物学作用机理的应变和非应变系统。构效关系主要集中在苯并唑核心的生物立体异构和Ru(II)配合物中大肠菌素的置换上。应变的化合物在光照射后迅速弹出2-(2-吡啶基)-苯并唑配体,并且在暗光条件下对HL-60细胞系均具有强毒性。相比之下,未应变的Ru(II)配合物在不存在光的情况下是无毒的,在光照射后以纳摩尔浓度诱导的细胞毒性,并且能够光诱导DNA损伤。暗光和暗光IC50值的90-220倍差异提供了较大的潜在治疗窗口,可允许通过暴露于光来选择性靶向细胞。

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