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Synthesis, structural elucidation, DFT calculation, biological studies and DNA interaction of some aryl hydrazone Cr3+, Fe3+, and Cu2+ chelates

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ELSEVIER SCI LTD
DOI: 10.1016/j.compbiolchem.2022.107643

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Metal hydrazone chelates; Theoretical calculations; Antimicrobial; Anti-cancer; DNA interaction, Molecular Docking

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The current research focuses on the synthesis and characterization of four novel solid complexes using an aryl hydrazone ligand to treat Cr(III), Fe(III), and Cu(II) metal ions. The complexes exhibited good thermal stability and a six-coordination with octahedral geometry. Density Functional Theory (DFT) computations provided insights into the electrical and structural features of these metal chelates. The compounds showed various interactions with CT-DNA and demonstrated antibacterial and antioxidant activities.
The current research focuses on the treatment of Cr(III), Fe(III) and Cu(II) metal ions with aryl hydrazone ligand named (E)-4-(((diphenylmethylene)hydrazono)methyl)benzene-1,3-diol (DPHB) to afford four novel solid complexes with high yields. Different characterization approaches, including infrared, UV-visible, and NMR spectroscopies, elemental analyses, and thermal gravimetric analysis (TGA), revealed that all mononuclear crystalline metal chelates with good thermal stability had a six-coordination with octahedral geometry. Density Functional Theory (DFT) computations were used and provided a reasonable explanation for these metal chelates' electrical and structural features. Furthermore, investigations of electronic absorption spectroscopy, hydrodynamics, and electrophoresis demonstrated that these new compounds interact with calf thymus deoxyribonucleic acid (CT-DNA) in a variety of ways. As a result, the K-b and Delta G(b)(not equal) values of such interactions were in the following order: DPHBCu > DPHBCr > DPHBFe complex. Additionally, the novel metal chelates have been studied antibathogenically and found to be significantly effective compared to the comparable DPHB hydrazone ligand. The anti-proliferative activities of the investigated compounds were also evaluated against different lines of cancer cells and exhibited significant cytotoxic activity. In addition, observations of antioxidant activity suggest that antioxidant activity relative to ordinary ascorbic acid was demonstrated in the molecule.

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