Synthesis, characterization and cytotoxicity studies of Co(III)-flavonolato complexes

Hypoxia activated Co(III) complexes as prodrugs may provide with a selective delivery of cytotoxic or antibacterial compounds. Whithin this field sixteen novel Co(III) ternary complexes with the general formula [Co(4N)(flav)](ClO4)2, where 4N = tris(2-aminoethyl)amine (tren) or tris(2-pyridylmethyl)...

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Veröffentlicht in:Journal of inorganic biochemistry 2021-04, Vol.217, p.111382-111382, Article 111382
Hauptverfasser: Kozsup, Máté, Zhou, XueQuan, Farkas, Etelka, Bényei, Attila Cs, Bonnet, Sylvestre, Patonay, Tamás, Kónya, Krisztina, Buglyó, Péter
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container_title Journal of inorganic biochemistry
container_volume 217
creator Kozsup, Máté
Zhou, XueQuan
Farkas, Etelka
Bényei, Attila Cs
Bonnet, Sylvestre
Patonay, Tamás
Kónya, Krisztina
Buglyó, Péter
description Hypoxia activated Co(III) complexes as prodrugs may provide with a selective delivery of cytotoxic or antibacterial compounds. Whithin this field sixteen novel Co(III) ternary complexes with the general formula [Co(4N)(flav)](ClO4)2, where 4N = tris(2-aminoethyl)amine (tren) or tris(2-pyridylmethyl)amine (tpa) and flav = deprotonated form of differently substituted flavonols have been synthesized, characterized, and their cytotoxicity assayed under both normoxic and hypoxic conditions. Molecular structures of two free flavonols and seven complexes are also reported. In all the complexes the bioligands exhibited the expected (O,O) coordination mode and the complexes showed a slightly distorted octahedral geometry. Cyclic voltammetric studies revealed that both the substituents of the flavonoles and the type of 4N donor ligands had an impact on the reduction potential of the complex. The ones containing tren demonstrated significantly higher stability than the tpa analogues, making these former compounds promising candidates for the development of hypoxia-activated prodrug complexes. Tpa complexes showed higher activity against both selected human cancer cell lines (A549, A431) than their free ligand flavonols, indicating that the anticancer activity of the bioligand can be enhanced upon complexation. However, slight hypoxia-selectivity was found only for a tren complex (11) with moderate cytotoxicity. Novel, multitargeted Co(III) complexes with flavonolate and ancillary 4N donor ligands have been synthesized, characterized and tested against selected human derived cancer cell lines under hypoxic and normoxic conditions. [Display omitted] •Synthesis of [CoIII(4N)(flavonolato)]2+ type complexes with flavonoles as bioligands.•Chemical characterization of the novel complexes including X-ray studies.•Dependence of the redox behavior of the complexes on the tripodal tetramine (4N).•Biological assay of the complexes against A549 and A431 cancer cell lines.
doi_str_mv 10.1016/j.jinorgbio.2021.111382
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Whithin this field sixteen novel Co(III) ternary complexes with the general formula [Co(4N)(flav)](ClO4)2, where 4N = tris(2-aminoethyl)amine (tren) or tris(2-pyridylmethyl)amine (tpa) and flav = deprotonated form of differently substituted flavonols have been synthesized, characterized, and their cytotoxicity assayed under both normoxic and hypoxic conditions. Molecular structures of two free flavonols and seven complexes are also reported. In all the complexes the bioligands exhibited the expected (O,O) coordination mode and the complexes showed a slightly distorted octahedral geometry. Cyclic voltammetric studies revealed that both the substituents of the flavonoles and the type of 4N donor ligands had an impact on the reduction potential of the complex. The ones containing tren demonstrated significantly higher stability than the tpa analogues, making these former compounds promising candidates for the development of hypoxia-activated prodrug complexes. Tpa complexes showed higher activity against both selected human cancer cell lines (A549, A431) than their free ligand flavonols, indicating that the anticancer activity of the bioligand can be enhanced upon complexation. However, slight hypoxia-selectivity was found only for a tren complex (11) with moderate cytotoxicity. Novel, multitargeted Co(III) complexes with flavonolate and ancillary 4N donor ligands have been synthesized, characterized and tested against selected human derived cancer cell lines under hypoxic and normoxic conditions. 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Tpa complexes showed higher activity against both selected human cancer cell lines (A549, A431) than their free ligand flavonols, indicating that the anticancer activity of the bioligand can be enhanced upon complexation. However, slight hypoxia-selectivity was found only for a tren complex (11) with moderate cytotoxicity. Novel, multitargeted Co(III) complexes with flavonolate and ancillary 4N donor ligands have been synthesized, characterized and tested against selected human derived cancer cell lines under hypoxic and normoxic conditions. 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subjects Anticancer
Antineoplastic Agents - chemical synthesis
Antineoplastic Agents - pharmacology
Cell Hypoxia - physiology
Cell Line, Tumor
Cobalt - chemistry
CoIII complexes
Coordination Complexes - chemical synthesis
Coordination Complexes - pharmacology
Flavonoids - chemical synthesis
Flavonoids - pharmacology
Flavonoles
Humans
Hypoxia activation
Ligands
Molecular Structure
Oxidation-Reduction
Redox behavior
Stereoisomerism
X-ray structures
title Synthesis, characterization and cytotoxicity studies of Co(III)-flavonolato complexes
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