Novel complexes with ONNO tetradentate coumarin schiff-base donor ligands: x-ray structures, DFT calculations, molecular dynamics and potential anticarcinogenic activity

被引:16
作者
Mestizo, Paula Daniela [1 ]
Narvaez, Diana M. [2 ]
Pinzon-Ulloa, Jesus Alberto [2 ]
Di Bello, Daniela Torres [2 ]
Franco-Ulloa, Sebastian [3 ]
Macias, Mario A. [1 ]
Groot, Helena [2 ]
Miscione, Gian Pietro [3 ]
Suescun, Leopoldo [4 ]
Hurtado, John J. [1 ]
机构
[1] Univ Los Andes, Dept Quim, Carrera 1 18A-12, Bogota 111711, Colombia
[2] Univ Los Andes, Human Genet Lab, Carrera 1 18A-12, Bogota 111711, Colombia
[3] Univ Los Andes, COBO Computat Bioorgan Chem, Chem Dept, Carrera 1 18A-12, Bogota 111711, Colombia
[4] Univ La Republ, Cryssmat Lab, Catedra Fis, DETEMA,Fac Quim, Montevideo, Uruguay
关键词
Bioinorganic chemistry; Anticarcinogenic activity; Coumarin schiff base ligands; G-quadruplex DNA; Structure elucidation; G-QUADRUPLEX DNA; METAL-COMPLEXES; COORDINATION-COMPOUNDS; INFRARED-SPECTRA; CYTOTOXICITY; COPPER(II); TRANSITIONS; ENERGIES; CRYSTAL; CO(II);
D O I
10.1007/s10534-020-00268-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The synthesis of eight novel Zn(II), Co(II), Cu(II), Ni(II) and Pt(II) complexes (2-9) derived from the ONNO tetradentate coumarin Schiff-Base donor ligands, L-1 and the novel L-2, was performed. All compounds were characterized by analytical, spectrometry and spectroscopy techniques. Complexes 2-4 were also characterized by DFT calculations and the structures of 5 and 6 were determined by single-crystal X-ray diffraction analysis. A cytotoxicity study was carried out through an MTT assay in the carcinogenic cell line HeLa and the noncarcinogenic cell lines HFF-1 and HaCaT. The results indicated that among all the evaluated compounds, 2 and 6 presented the best anticarcinogenic potential against HeLa cells with an IC50 of 3.5 and 4.1 mu M, respectively. In addition, classical molecular dynamics simulations were performed on the synthesized coordination compounds bound to G4 DNA architectures in the scope of shedding light on their inhibition mode and the most conserved interactions that may lead to the biological activity of the compounds.
引用
收藏
页码:119 / 140
页数:22
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