Biological evaluation, DFT, MEP, HOMO-LUMO analysis and ensemble docking studies of Zn(II) complexes of bidentate and tetradentate Schiff base ligands as antileukemia agents

被引:74
作者
Akbari, Zahra [1 ,2 ]
Stagno, Claudio
Iraci, Nunzio
Efferth, Thomas [3 ]
Omer, Ejlal A.
Piperno, Anna
Montazerozohori, Morteza [1 ]
Feizi-Dehnayebi, Mehran [4 ]
Micale, Nicola [2 ]
机构
[1] Univ Yasuj, Dept Chem, Yasouj 7591874831, South Korea
[2] Univ Messina, Dept Chem Biol Pharmaceut & Environm Sci, Viale Ferdinando Stagno Alcontres 31, I-98166 Messina, Italy
[3] Johannes Gutenberg Univ Mainz, Inst Pharmaceut & Biomed Sci, Dept Pharmaceut Biol, Staudinger Weg 5, D-55128 Mainz, Germany
[4] Univ Sistan & Baluchestan, Dept Chem, POB 98135-674, Zahedan, Iran
关键词
Zn(II) complexes; Antileukemia agents; DFT; MEP; Docking; HIRSHFELD SURFACE; CRYSTAL-STRUCTURE; METAL-COMPLEXES; DNA; CYTOTOXICITY; RECOGNITION;
D O I
10.1016/j.molstruc.2023.137400
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 Schiff base ligands and some related bidentate and tetradentate Zn(II) complexes were investigated for their biological activity profiles as anticancer agents by resazurin method against two leukemia cell lines. The results clearly evidenced the importance of the tetradentate structure and the presence of the metal ion on the cytotoxicity profile of these complexes. Noteworthy, they also showed an interesting selectivity index (SI; up to 15.1 for the complex [ZnL4(NO3)2] assessed on PBMC cells). The electronic behavior, stable geometries, MEP surfaces, and FMO analysis of the compounds were investigated employing density functional theory (DFT) at B3LYP level with LANL2DZ/6-311G(d,p) basic set. A comparison was made with the computational and experimental structural data of L2 and [ZnL2(NO3)2] compounds. Furthermore, ensemble docking studies were undertaken on a quadruplex-duplex (Q-D) DNA model to shed light on the interactions at molecular level of the complexes with the target. In silico ADME profiling was performed using the SwissADME program, which indicated their promising therapeutic applicability.
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页数:11
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