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Updated: Sep 17, 2025
Anticancer Metal Complexes: Synthesis and Cytotoxicity Evaluation by the MTT Assay
Published on: November 10, 2013
Salen-Type Copper(II) Complexes: Synthesis, Characterization, Computational Studies, Molecular Docking, Anticancer
Abdellatif A Helaly1,2, Bandar A Babgi1, Yoji Kobayashi3
1Department of Chemistry, Faculty of Science, King Abdulaziz University (KAU), Jeddah, 21589, Saudi Arabia.
None:
Transition metal complexes are considered a significant treatment for cancer diseases because of their efficacy toward cancer cells. However, most of these compounds have limited potential toward cancer cells due to their organic backbone structure. Here, the synthesis and anticancer screening of three different ligand structures of salen copper(II) complexes are reported: [CuII(salophen)(H2O)2] (1), [CuII(salen)(H2O)2] (2), and [CuII(etho-salen)(H2O)2] (3). Using density functional theory-optimized structures, docking active site interactions are evaluated to predict the activity of salen-type ligands and their copper(II) complexes against cyclin-dependent kinase 5 (Cdk5 ) and aromatase cytochrome (P450) proteins. The molecular docking study reveals that among all studied ligands and complexes, [CuII(salen)(H2O)2] (2) has the best docking score value, S = -8.79 and -7.73, with the lowest root mean square deviation (RMSD = 1.02 and 1.09) against proteins Cdk5 and P450, respectively. Anticancer activity against MCF-7 and HCT-116 cell lines reveals that [CuII(salen)(H2O)2] (2) shows favorable behavior with IC50 values of 212.5 and 98.9 μm, respectively. Its parent ligand 2 shows lower potency, with IC50 values of 404.7 μm in MCF-7 and 305.2 μm in HCT-116. Notably, copper(II) complexes display reduced toxicity rather than cisplatin toward normal HFF-1 fibroblasts, indicating a more favorable therapeutic window.
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