光动力疗法
亚胺
二胺
DNA
化学
癌细胞
癌症
连接器
共价键
细胞凋亡
立体化学
组合化学
生物
生物化学
高分子化学
遗传学
有机化学
催化作用
操作系统
计算机科学
作者
Xuezhao Li,Jinguo Wu,Lei Wang,Cheng He,Liyong Chen,Yang Jiao,Chunying Duan
标识
DOI:10.1002/anie.201915281
摘要
The development of DNA-targeted photodynamic therapy (PDT) agents for cancer treatment has drawn substantial attention. Herein, the design and synthesis of dinuclear IrIII -containing luminescent metallohelices with tunable PDT efficacy that target mitochondrial DNA in cancer cells are reported. The metallohelices are fabricated using dynamic imine-coupling chemistry between aldehyde end-capped fac-Ir(ppy)3 handles and linear alkanediamine spacers, followed by reduction of the imine linkages. The length and odd-even character of the diamine alkyl linker determined the stereochemistry (helicates vs. mesocates). Compared to the helicates, the mesocates exhibit improved apoptosis-induction upon white-light irradiation. Molecular docking studies indicate that the mesocate with a proper length of diamine spacers shows stronger affinity for the minor groove of DNA. This study highlights the potential of DNA-targeting IrIII -containing metallohelices as PDT agents.
科研通智能强力驱动
Strongly Powered by AbleSci AI