Syntheses, structures, Hirshfeld surface analyses, BSA interactions and molecular docking studies of two leucine Schiff base complexes of oxovanadium(IV)

被引:0
|
作者
Dong, Jianfang [1 ,2 ]
Guo, Qiong [1 ]
Zhao, Peiran [3 ]
Gao, Lei [3 ]
Jing, Buqin [4 ]
Li, Lianzhi [1 ]
机构
[1] Liaocheng Univ, Coll Chem & Chem Engn, Liaocheng 252059, Peoples R China
[2] Shandong Polytech Technician Coll, Liaocheng 252027, Peoples R China
[3] Liaocheng Peoples Hosp, Dept Nucl Med, Liaocheng 252000, Shandong, Peoples R China
[4] Shanxi Datong Univ, Coll Chem & Chem Engn, Datong 037009, Peoples R China
关键词
Oxovanadium(IV) complexes; Leucine Schiff base; Crystal structure; BSA interaction; BOVINE SERUM-ALBUMIN; CRYSTAL-STRUCTURE; DNA-BINDING; FLUORESCENCE; CHEMISTRY; VANADIUM;
D O I
10.1016/j.molstruc.2023.136446
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
Two mixed-ligand oxovanadium(IV) complexes with a Schiff base derived from o-vanillin and leucine and 1,10-phenanthroline or 2,2 '-bipyridine as a co-ligand, [VO(o-van-Leu)phen] (1) and [VO(o-van-Leu)bipy]center dot H2O (2), were prepared and structurally characterized by IR spectra, elemental analyses and single-crystal X-ray diffraction. The crystal structures reveal that each oxovanadium(IV) atom in complexes 1 and 2 is surrounded by a N3O3 coordination sphere to form a distorted octahedron with a Schiff base and neutral bidentate ligand phen or bipy. Hirshfeld surface analyses and 2D fingerprint plots indicated that the molecular packings in crystals were dominated by H center dot center dot center dot H, O center dot center dot center dot H/H center dot center dot center dot O, C center dot center dot center dot H/H center dot center dot center dot C and p- p interactions. The interactions of both complexes with bovine serum albumin (BSA) were studied by using various spectroscopic and molecular docking methods. BSA binding constants (K), estimated by UV-Vis spectroscopy, were 2.53 x 10(4) M 1 for 1 and 3.18 x 104 M 1 for 2, respectively. Together with results of fluorescence and CD spectral studies, it showed that complex 2 has a better affinity for BSA than complex 1. Molecular docking investigation indicated that the two complexes had the similar mode of binding and located within subdomain IIA of BSA. Complex 2 had greater binding activity with the binding free energy (Delta G(binding)) of -6.5 kcal/mol than Complex 1 with Delta G(binding) of-5.42 kcal/mol, consisting with the analyses of spectroscopic experimental results.
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页数:11
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