Silver(I) Complexes with Mefenamic Acid and Nitrogen Heterocyclic Ligands: Synthesis, Characterization, and Biological Evaluation

被引:0
|
作者
Zhang, Lu-Lin [1 ]
Huang, Xiang [1 ]
Azam, Mohammad [2 ]
Yuan, Hua-Xin [1 ]
Ma, Feng-Jie [1 ]
Cheng, Yuan-Zheng [1 ]
Zhang, Li-Ping [1 ]
Sun, Di [3 ]
机构
[1] Shandong Second Med Univ, Sch Pharm, Weifang 261053, Peoples R China
[2] King Saud Univ, Coll Sci, Dept Chem, PO Box 2455, Riyadh 11451, Saudi Arabia
[3] Shandong Univ, State Key Lab Crystal Mat, Sch Chem & Chem Engn, Jinan 250100, Peoples R China
关键词
NONSTEROIDAL ANTIINFLAMMATORY DRUGS; IN-VITRO; ANTICANCER ACTIVITY; DNA-BINDING; DICARBOXYLATE COMPLEXES; COORDINATION POLYMER; SALICYLIC-ACID; NSAIDS; DICLOFENAC; ANTIOXIDANT;
D O I
10.1021/acs.inorgchem.4c01766
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Four Ag(I) complexes with mefenamato and nitrogen heterocyclic ligands, [Ag(2-apy)(mef)](2) (1), [Ag(3-apy)(mef)] (2), [Ag-2(tmpyz)(mef)(2)] (3), and {[Ag(4,4 '-bipy)(mef)](2)(CH3CN)(1.5)(H2O)(2)}(n) (4), (mef = mefenamato, 2-apy = 2-aminopyridine, 3-apy = 3-aminopyridine, tmpyz = 2,3,5,6-tetramethylpyrazine, 4,4 '-bipy = 4,4 '-bipyridine), were synthesized and characterized. The interactions of these complexes with BSA were investigated by fluorescence spectroscopy, which indicated that these complexes quench the fluorescence of BSA by a static mechanism. The fluorescence data also indicated that the complexes showed good affinity for BSA, and one binding site on BSA was suitable for the complexes. The in vitro cytotoxicity of the four complexes against human cancer cell lines (MCF-7, HepG-2, A549, and MDA-MB-468) and one normal cell line (HTR-8) was evaluated by the MTT assay. Complex 1 displayed high cytotoxic activity against A549 cells. Further studies revealed that complex 1 could enhance the intracellular levels of ROS (reactive oxygen species) in A549 cells, cause cell cycle arrest in the G0/G1 phase, and induce apoptosis in A549 cells in a dose-dependent manner.
引用
收藏
页码:12624 / 12634
页数:11
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