1. Synthesis of the first mixed ligand Mn (II) and Cd (II) complexes of 4‐methoxy‐pyridine‐2‐carboxylic acid, molecular docking studies and investigation of their anti‐tumor effectsin vitro
- Author
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Hayatullah Mahmoody, Ömer Tamer, Olca Kilinc, Necmi Dege, Oya Orun, Kağan Fehmi Feyzioğlu, Davut Avcı, Yusuf Atalay, and Ondokuz Mayıs Üniversitesi
- Subjects
Antitumor activity ,chemistry.chemical_classification ,crystal structure ,Stereochemistry ,Carboxylic acid ,molecular docking ,General Chemistry ,Mixed ligand ,Crystal structure ,DFT ,In vitro ,Inorganic Chemistry ,chemistry.chemical_compound ,4-methoxy-pyridine-2-carboxylic acid ,chemistry ,Pyridine ,anti-tumor activity - Abstract
WOS: 000504006700001 The first mixed ligand Mn (II) and Cd (II) complexes containing 4-methoxy-pyridine-2-carboxylic acid (4-mpic) and 4,4 '-dimethyl-2,2 '-bipyridine (dmbpy) were synthesized in this study. The geometric structures of [Mn(4-mpic)(2)(dmbpy)] (complex 1) and [Cd(4-mpic)(2)(dmbpy)] (complex 2) were determined by single crystal X-Ray diffraction method. FT-IR and UV-Vis spectra were also recorded to investigate vibrational and electronic properties of complexes 1 and 2. Density functional theory (DFT) calculations were also carried out to provide a deep understanding in geometric, spectroscopic, electronic and nonlinear optical (NLO) properties of complexes 1 and 2. The first-order hyperpolarizibility (beta) parameter calculated as 332.9736 x 10(-30) esu demonstrated that complex 1 is an extremely promising candidate to NLO materials. Natural bond orbital (NBO) analysis not only verified the distorted octahedral geometries of central metal ions, but also found out the high-energy interactions responsible for biological activities for complexes 1 and 2. Anti-cancer activities of complexes 1 and 2 were tested on human breast carcinoma cell line MCF-7 (ER and PR positive, HER2 negative) and the triple negative breast carcinoma cell line MDA-MB 231 (ER, PR and HER2 negative). Dose-response relationship derived from MTT assays indicates that complexes 1 and 2 are showing concentration-dependent effects, which could suggest a potential use for these drug combinations in cancer cell lines.
- Published
- 2019
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