Synthesis, characterization, anticancer activity, and molecular docking study of some metal complexes with a new Schiff base ligand

被引:14
|
作者
Alorini, Thamer [1 ]
Daoud, Ismail [2 ,3 ]
Al-Hakimi, Ahmed N. [1 ,4 ]
Alminderej, Fahad [1 ]
机构
[1] Qassim Univ, Coll Sci, Dept Chem, Buraydah 51452, Saudi Arabia
[2] Univ Abou Bakr Belkaid, Fac Sci, Dept Chem, Lab Nat Subst & Bioact LASNABIO Tlemcen Algeria, Tilimsen, Algeria
[3] Univ Mohamed Khider Biskra, Dept Matter Sci, BP 145 RP, Biskra 07000, Algeria
[4] Ibb Univ, Coll Sci, Dept Chem, Ibb, Yemen
关键词
Schiff base complex; Anticancer activity; Molecular docking; X-RAY-STRUCTURE; SPECTROSCOPIC CHARACTERIZATION; BIOLOGICAL-ACTIVITY; CRYSTAL-STRUCTURES; DNA-BINDING; 2-AMINOMETHYLBENZIMIDAZOLE; TOXICITY; DESIGN;
D O I
10.1016/j.molstruc.2022.134785
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
2-((E)-((4-(((E)-4-methoxybenzylidene)amino)phenyl)imino)methyl)naphthalen-1-ol, a new Schiff base ligand, was made and then metalated with number of metal ions. The compounds were characterized by various techniques. The result confirmed that the ligand coordinated with the metals in a bidentate nature, through azomethine nitrogen and phenolic oxygen atom; and gave an octahedral geometry. The XRD patterns of the ligand and complexes of Fe(III), Co(III), and Zn(II) have a crystalline nature, while the Ni(II), and Cu(II) complexes have an amorphous structure. The antibacterial and antifungal effects were investigated. It was observed that the Zn(II) and Fe(III) complexes had the highest activity among the compounds against S. enterica ser. typhi and C. albicans, respectively. The IC50 values demonstrated that the Ni(II) complex displayed the highest activity against A549, HepG-2, and PC-3 cancer cell lines. Fur-thermore, molecular docking simulation revealed that the Zn(II), Co(III), and Ni(II) complexes were shown to have a high binding affinity with the active sites targets of S. enterica ser. typhi bacteria and C. albi-cans fungi strains, and the active sites of three targets in the cancer cell lines A549, HepG-2, and PC-3, respectively. (c) 2022 Elsevier B.V. All rights reserved.
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页数:16
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