POCOP-Ni(II) pincer compounds derived from phloroglucinol. Cytotoxic and antioxidant evaluation

POCOP-Ni(II) pincer compounds have primarily been explored as catalysts, but their potential biological activity has been scarcely studied. To address this gap, we evaluated the anticancer and antioxidant potential of four POCOP-Ni(II) complexes derived from phloroglucinol. A comprehensive supramole...

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Bibliographic Details
Published in:Frontiers in chemistry Vol. 12
Main Authors: Amaya-Flórez, Andrés, Serrano-García, Juan S., Ruiz-Galindo, Jordi, Arenaza-Corona, Antonino, Cruz-Navarro, J. Antonio, Orjuela, Adrian L., Alí-Torres, Jorge, Flores-Alamo, Marcos, Cano-Sanchez, Patricia, Reyes-Márquez, Viviana, Morales-Morales, David
Format: Journal Article
Language:English
Published: Frontiers Media S.A 20-11-2024
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Summary:POCOP-Ni(II) pincer compounds have primarily been explored as catalysts, but their potential biological activity has been scarcely studied. To address this gap, we evaluated the anticancer and antioxidant potential of four POCOP-Ni(II) complexes derived from phloroglucinol. A comprehensive supramolecular analysis, based on single-crystal X-ray diffraction (DRX) structures, was conducted using Hirshfeld surfaces and non-covalent interaction analysis. The cytotoxicity of all complexes was systematically assessed against various cancerous cell lines, as well as a non-cancerous cell line (COS-7). The results revealed that complexes 1b and 1c exhibited remarkable antiproliferative activity, with IC 50 values ranging from 2.43 to 7.85 μM against cancerous cell lines U251, K562, HCT-15, MCF-7, and SK-LU-1. To further elucidate their mechanism of action, a competitive fluorescence displacement assay with ethidium bromide (EB) suggested that these complexes possess the ability to intercalate with DNA. This multifaceted investigation not only enhances our understanding of the biological potential of POCOP-Ni complexes but also provides valuable insights into their structural features and interactions, paving the way for future exploration in both catalytic and therapeutic domains.
ISSN:2296-2646
2296-2646
DOI:10.3389/fchem.2024.1483999