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Photoactivated DNA cleavage and anticancer activity of oxovanadium(IV) complexes of curcumin

机译:姜黄素氧钒(IV)配合物的光活化DNA切割和抗癌活性

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Oxovanadium(IV) complexes [VO(Fc-pic)(acac)](ClO_4) (1), [VO(Fc-pic)(cur)](ClO_4) (2), [VO(Ph-pic)(acac)](ClO_4) (3) and [VO(Ph-pic)(cur)](ClO_4) (4), where Fc-pic and Ph-pic are ferrocenylmethyl-bis-(2-pyridylmethylamine) (in 1, 2) and bis-(2-pyridylmethyl) benzylamine (in 3, 4), respectively, acac is acetylacetonate anion (in 1, 3) and cur is curcumin anion (in 2, 4) were prepared, characterized and their photo-induced DNA cleavage and anticancer activity studied. The crystal structure of 1 as its PF_6 ~- salt (1a) shows the presence of a VO~(2+) moiety in VO_3N_3 coordination geometry. The complexes show a d-d band at ~790 nm in DMF and display V(IV)/V(III) redox couple near -1.45 V vs. SCE in DMF-0.1 M TBAP. The complexes are avid binders to calf thymus DNA. Complex 2 efficiently photo-cleaves plasmid DNA in near-IR light of 785 nm forming OH radicals. The curcumin complexes show photocytotoxicity in HeLa cancer cells in visible light of 400-700 nm with significant cellular uptake within 4 h of incubation time.
机译:氧钒(IV)络合物[VO(Fc-pic)(acac)](ClO_4)(1),[VO(Fc-pic)(cur)](ClO_4)(2),[VO(Ph-pic)(acac) )](ClO_4)(3)和[VO(Ph-pic)(cur)](ClO_4)(4),其中Fc-pic和Ph-pic是二茂铁基甲基-双-(2-吡啶基甲胺)(在1,2 )和双-(2-吡啶基甲基)苄胺(分别在3,4中),制备了acac是乙酰丙酮阴离子(在1,3中)和cur是姜黄素阴离子(在2,4中),对其进行了表征和光诱导DNA裂解和抗癌活性进行了研究。 1的晶体结构为PF_6〜-盐(1a),表明在VO_3N_3配位几何结构中存在VO〜(2+)部分。在DMF-0.1 M TBAP中,复合物在〜790 nm处显示d-d带,并在-1.45 V附近显示V(IV)/ V(III)氧化还原对。该复合物是小牛胸腺DNA的狂热结合物。复合物2在785 nm的近红外光中有效地裂解质粒DNA,形成OH自由基。姜黄素复合物在HeLa癌细胞中在400-700 nm的可见光中显示出光细胞毒性,并且在孵育时间4小时内具有明显的细胞摄取。

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