Preparation, characterization, DNA/BSA interaction and computational binding analyses of a dinuclear, biopotency Pd+2 coordinated with 1,4-phenylenediamine and ethylenediamine as ligands

被引:12
作者
Afisufi, Narjes [1 ]
Mansouri-Torshizi, Hassan [1 ]
机构
[1] Univ Sistan & Baluchestan, Fac Sci, Dept Chem, Zahedan, Iran
关键词
Dinuclear-Pd(II) complex; Cytotoxicity; DNA; and BSA-binding studies; Molecular Docking; HUMAN SERUM-ALBUMIN; DNA-BINDING; PALLADIUM(II) COMPLEXES; IN-VITRO; PLATINUM(II) COMPLEXES; ANTIMICROBIAL ACTIVITY; CYTOTOXICITY; DERIVATIVES; GROOVE; 2,2'-BIPYRIDINE;
D O I
10.1007/s13738-020-02098-4
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A novel, dinuclear and dissolvable palladium(II) complex of [{Pd(en)Cl}(2)(mu-p-ph-da)](NO3)(2), where en is ethylenediamine and p-ph-da is 1,4-phenylenediamine, was synthesized by the reaction between [Pd(en)(dmf)Cl](NO3) (dmf = dimethyl formamide) and p-ph-da in the molar ratio of 2:1. The structure and formulation of the complex were also proposed on the bases of elemental analysis, conductivity measurements, and spectral (FT-IR, UV-Vis, and NMR (H-1 and D2O exchange)) data. The complex was screened for its antitumor activity against MOLT-4 have shown a significant decrease in viability after 24 h which was also dose-dependent. Rich CT-DNA and BSA interaction studies including absorption, fluorescence, thermodynamic, energy transfer, electrophoresis, cyclic voltammetry, and circular dichroism revealed that hydrogen-binding, van der Waals, and electrostatic attractions are different binding forces for the complex interacting with the above biomacromolecules. Likewise, molecular docking simulation supports the above experimental conclusions.
引用
收藏
页码:1147 / 1166
页数:20
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