Palladium (II) complexes containing substituted thiosemicarbazones. Synthesis, spectral characterization, X-ray crystallography, biomolecular interactions and in vitro cytotoxicity

被引:20
作者
Anu, D. [1 ]
Naveen, P. [1 ]
Rath, Nigam P. [2 ]
Kaveri, M., V [1 ]
机构
[1] Bharathiar Univ, Dept Chem, Coimbatore 641046, Tamil Nadu, India
[2] Univ Missouri, Dept Chem & Biochem, St Louis, MO 63121 USA
关键词
Pd (II) complexes; Spectroscopy; Single crystal X-ray; DNA/ protein binding; Anti-oxidant and cytotoxicity; TRANSITION-METAL-COMPLEXES; DNA-BINDING; STRUCTURAL-CHARACTERIZATION; PLATINUM(II) COMPLEXES; NICKEL(II) COMPLEXES; ANTIOXIDANT ACTIVITY; DNA/PROTEIN BINDING; CRYSTAL-STRUCTURES; PROTEIN-BINDING; ANTICANCER;
D O I
10.1016/j.molstruc.2020.127703
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
Palladium (II) complexes were synthesized from 4(N)-substituted thosemicarbazones schiff base ligands. The new complexes were confirmed by analytical, various spectroscopic techniques and single crystal X-ray crystallography. Crystallographic studies exhibited that the complexes 2 and 3 distorted square planar geometry around palladium metal ion. All the complexes are proved their DNA/protein binding ability by using absorption and emission titrations. Investigations of antioxidant properties showed that all the complexes have significant radical scavenging properties. The anticancer activity of Pd(II) complexes was probed in vitro cytotoxicity against human breast (MCF7) and lung (A549) cancer cell lines by MTT assay. Further, AO/EB and DAPI staining methods were carried out to detect the cell death induced by the complexes. Among all the complexes, complex 1 exhibited better cytotoxic activity. (C) 2020 Elsevier B.V. All rights reserved.
引用
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页数:12
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