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混合配体单核铜(II)配合物:晶体结构与抗癌活性

Mixed-ligand mononuclear copper(II) complex: crystal structure and anticancer activity.

作者信息

Qin Xiu-Ying, Liu Ya-Nan, Yu Qian-Qian, Yang Li-Cong, Liu Ying, Zhou Yan-Hui, Liu Jie

机构信息

Department of Chemistry, Jinan University, Guangzhou 510632, China; College of Pharmacy, Guilin Medical University, Guilin 541004 (China).

出版信息

ChemMedChem. 2014 Aug;9(8):1665-71. doi: 10.1002/cmdc.201402060. Epub 2014 May 19.

Abstract

A novel copper(II) complex with mixed ligands including β-[(3-formyl-5-methyl-2-hydroxy-benzylidene)amino]propionic acid anion and 1,10'-phenanthroline was synthesized, and its crystal structure was thoroughly characterized. It exerted excellent inducing apoptosis, anti-angiogenesis and antiproliferative properties in vitro. The complex can bind human serum albumin (HSA) at physiological pH conditions. Remarkably, it can induce formation of the mixed parallel/antiparallel G-quadruplex structures in the G-rich sequence of the proximal vascular endothelial growth factor (VEGF) promoter, and stabilize these G-quadruplex structures, which provide an opportunity for anti-angiogenesis chemotherapeutics. Furthermore, the complex showed a strong uptake, and exhibited multiple anticancer functions by inhibiting the expression of p-Akt and p-Erk1/2 proteins and by upregulating the levels of reactive oxygen species (ROS). Because of the reported results, this new copper(II) complex qualifies itself as a potential anticancer drug candidate.

摘要

合成了一种新型的含β-[(3-甲酰基-5-甲基-2-羟基-亚苄基)氨基]丙酸阴离子和1,10'-菲咯啉混合配体的铜(II)配合物,并对其晶体结构进行了全面表征。该配合物在体外具有优异的诱导凋亡、抗血管生成和抗增殖特性。在生理pH条件下,该配合物能与人血清白蛋白(HSA)结合。值得注意的是,它能在近端血管内皮生长因子(VEGF)启动子的富含G的序列中诱导形成混合的平行/反平行G-四链体结构,并稳定这些G-四链体结构,这为抗血管生成化疗药物提供了契机。此外,该配合物表现出强烈的摄取,并通过抑制p-Akt和p-Erk1/2蛋白的表达以及上调活性氧(ROS)水平发挥多种抗癌功能。基于所报道的结果,这种新型铜(II)配合物有资格成为一种潜在的抗癌药物候选物。

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