Juglone-based complexes demonstrate enhanced selectivity and cytotoxicity against cancer cells, indicating potential therapeutic benefits.
Four Juglone-based Pd(0) complexes with varied ligands were synthesized and characterized. They showed strong cytotoxicity and cancer selectivity. The most promising complex inhibited the PIN1 oncoprotein, as confirmed by Western Blot.
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Tonon et al. (2025) studied this question.
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