Homoleptic bisterpyridyl complexes: Synthesis, characterization, DNA binding, DNA cleavage and topoisomerase II inhibition activity

被引:18
作者
Sinha, Priti [1 ]
Kumari, Niraj [1 ]
Singh, Kanhaiya [2 ]
Singh, Kiran [2 ]
Mishra, Lallan [1 ]
机构
[1] Banaras Hindu Univ, Fac Sci, Dept Chem, Varanasi 221005, Uttar Pradesh, India
[2] Banaras Hindu Univ, Mol & Human Genet, Varanasi 221005, Uttar Pradesh, India
关键词
Terpyridine; X-ray diffraction; Chemical nuclease; Cytotoxicity; Topoisomerase II inhibition; COPPER(II) COMPLEXES; MOLECULAR DOCKING; CRYSTAL-STRUCTURE; NUCLEIC-ACIDS; IN-VITRO; LIGAND; RECOGNITION; TRANSITION; CANCER; PHOTOCLEAVAGE;
D O I
10.1016/j.ica.2015.03.026
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Octahedral complexes of type [Co(L)(2)]center dot 2NO(3) 1, [Co(L)(2)]center dot 3NO(3) 2 and [Zn(L)(2)]center dot 2NO(3) 3 (L = 4'-phenyl-2,2': 6',2 '' terpyridine) are synthesized and characterized using elemental analysis, NMR, IR, UV-Vis and fluorescence spectra and further supported by their X-ray diffraction studies. The binding properties of the complexes with DNA are carried out using UV-Vis, fluorescence titrations. Viscosity measurement supported partial intercalation of the complexes with DNA. Gel electrophoretic mobility assay of the complexes with Plasmid DNA (pBR322) shows that complex 1 binds with the major groove of double helical DNA. The molecular docking showed that complex 1 binds to DNA via groove binding in GC-rich sequence. It also inhibits topoisomerase II activity with IC50 value as 30. Other complexes do not bind DNA significantly. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:71 / 80
页数:10
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