Synthesis, characterization, potential antimicrobial, antioxidant, anticancer, DNA binding, and molecular docking activities and DFT on novel Co(II), Ni(II), VO(II), Cr(III), and La(III) Schiff base complexes

化学 一元酸 席夫碱 插层(化学) 螯合作用 配体(生物化学) 结合常数 抗氧化剂 滴定法 DNA 凝胶电泳 二聚体 立体化学 齿合度 核化学 金属 无机化学 结合位点 高分子化学 有机化学 生物化学 受体
作者
Laila H. Abdel‐Rahman,Maram T. Basha,Badriah Saad Al–Farhan,Mohamed R. Shehata,Ehab M. Abdalla
出处
期刊:Applied Organometallic Chemistry [Wiley]
卷期号:36 (1) 被引量:12
标识
DOI:10.1002/aoc.6484
摘要

In this study, five novel complexes for Co(II), Ni(II), VO(II), Cr(III), and La(III) ions were synthesized from a tridentate NNO monobasic chelating Schiff base ligand, (Z)‐2‐((pyridin‐2‐ylimino)methyl)phenol (HL). Spectral and analytical tools were applied to elucidate the structural compositions of the new compounds. Then, geometry optimization was conducted for all the syntheses by the Gaussian 09 program via the density functional theory method to obtain optimal structures and the most essential parameters. Moreover, the biochemical behaviors of all the syntheses were explored based on the reactivity, which was tested against various cancer cell lines (HepG‐2, MCF‐7, and HCT‐116). The complexes exhibited an interestingly antiproliferative potential against human cancer cell lines, and the cytotoxicities of the new complexes were arranged to follow the order: VOL > CrL > NiL > LaL > CoL > HL. The antioxidant behaviors of the complexes were studied using the DPPH assay, and VOL showed the maximum antioxidant activity, followed by LaL. The antibacterial activities of the HL ligand and its complexes were studied. Moreover, the binding nature of the complexes with calf thymus DNA (CT‐DNA) was investigated based on the spectrophotometric absorption titration, viscosity, and gel electrophoresis methods. The binding ability of the complexes with CT‐DNA was proposed to be just intercalation or replacement mode. The intrinsic binding constant K b was calculated and arranged based on the following order: VOL (5.2 × 10 5 ) > CrL (3.6 × 10 5 ) > NiL (3.3 × 10 5 ) > LaL (3.0 × 10 5 ) > CoL (1.12 × 10 5 ) mol −1 dm −3 . Docking investigations were performed using the receptors of COVID‐19's main protease viral protein (PDB ID: 6LU7) and Escherichia coli (gram [–ve] bacteria [PDB ID: 1fj4]).
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