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DOI 10.1021/acs.jmedchem.4c01220

Медицинская библиотека · Journal of medicinal chemistry · 2024

Enhancing Bioactivity of N,N,N-Chelating Rhodium(III) Complexes with Ionic Liquids: Toward Targeted Cancer Therapy.

Caković Angelina, Ćoćić Dušan, Živanović Marko, Janković Nenad, Milivojević Nevena, Delibašić Marija, Kostić Marina, Radojević Ivana, Grujović Mirjana, Marković Katarina G, Klisurić Olivera R, Vraneš Milan, Bogojeski Jovana

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

This study investigates the potential of using ionic liquids as cosolvents to enhance the solubility and activity of poorly soluble rhodium(III) complexes, particularly those with diene, pyridine derivatives, and camphor-derived bis-pyrazolylpyridine ligands, in relation to 5'-GMP, CT-DNA, and HSA as well as their biological activity. Findings indicate that ionic liquids significantly increase the substitution activity of these complexes toward 5'-GMP while only marginally affecting DNA/HSA binding affinities with molecular docking, further confirming the experimental results. Lipophilicity assessments indicated good lipophilicity. Notably, cytotoxicity studies show that Rh2 is selectively effective against HeLa cancer cells, with IL1 and IL10 modulating the cytotoxic effects. Redox evaluations indicate that rhodium complexes induce oxidative stress in cancerous cells while maintaining redox balance in noncancerous cells. By elucidating the role of ionic liquids in modulating these effects, the study proposes a promising avenue for augmenting the efficacy and selectivity of cancer treatments, thus opening new horizons in cancer therapeutics.

Для цитирования: Caković Angelina, Ćoćić Dušan, Živanović Marko, Janković Nenad, Milivojević Nevena, Delibašić Marija, Kostić Marina, Radojević Ivana, Grujović Mirjana, Marković Katarina G, Klisurić Olivera R, Vraneš Milan, Bogojeski Jovana. Enhancing Bioactivity of N,N,N-Chelating Rhodium(III) Complexes with Ionic Liquids: Toward Targeted Cancer Therapy.. Journal of medicinal chemistry. 2024. DOI: 10.1021/acs.jmedchem.4c01220.

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