SYNTHESIS AND STUDY OF CYTOTOXICITY OF HETEROLIGAND AZOLE-CONTAINING COMPLEXES Cu(II) and Co(II)
NXOUUH
DOI:
https://doi.org/10.25712/ASTU.2072-8921.2025.04.029%20Keywords:
ligands, azoles, complex compounds of copper and cobalt, inorganic salts, 2,2’-bipyridyl, synthesis, cytotoxicity, lymphoma cells, anticancer drugsAbstract
Various heterocyclic structures, including azole-containing coordination compounds of transition metal ions, are part of antitumor drugs. Currently, new methods to synthesize such drugs that damage and destroy rapidly proliferating cancer cells, are being developed. In this work, coordination compounds of copper(II) and cobalt(II) with 1-(benzimidazolyl)- 2-(3,5-dimethylpyrazole-1-yl) ethane, as well as multi-ligand complexes consisting of 2,2’-bipyridyl molecules, were obtained. All complexes have been studied as agents that suppress the proliferation of cancer cells. The study demonstrated that the obtained coordination compounds exhibit cytotoxicity against T-cell type lymphoma cells (JURKAT). It was experimentally established that in the control group (without the addition of the complex), after two days of cultivation in a thermostat, there were 10 times more cells than in the groups with the addition of the complexes. In addition, the obtained coordination compounds showed less cytotoxicity compared to inorganic salts of the corresponding metals, and are expected to have less negative effects on healthy cells, while interfering with the division of cancer cells.
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