Key result
Review outlines cytotoxicity and mechanisms of anticancer organoiridium complexes with Schiff base and oxime ligands.
Why the study?
There is a need for novel metal-based anticancer agents that reduce side effects, but only a limited number of reviews focus on the therapeutic potential of iridium complexes with specific ligand classes.
This review summarizes the antitumor properties, cytotoxicity, and mechanisms of action of iridium complexes with Schiff base and oxime ligands.
May inform design of iridium-based anticancer agents; leaves open clinical translation and efficacy trials.
Society has a pressing need for the development of novel metal‐based therapeutic agents that can mitigate the adverse side effects associated with current anticancer medications. In recent years, significant progress has been made in developing anticancer agents based on iridium organometallic complexes, where the coordinated organic ligands largely govern the biological activity. Therefore, the appropriate design of ligands is highly crucial in the development of effective metallodrugs for cancer therapy. Surprisingly, only a limited number of reviews are available in the literature which specifically focused on the cancer therapeutic potentials of iridium complexes with a particular class of ligands. This review provides a comprehensive overview of the antitumor properties of iridium complexes with Schiff base and oxime ligands. It provides an in‐depth discussion on the cytotoxicity and mechanisms of action of iridium complexes, comparative analyses with their ruthenium, rhodium and osmium analogs in several cases.
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Jadab et al. (2026) conducted a review in Cancer. Iridium complexes with Schiff base and oxime ligands vs. Ruthenium, rhodium and osmium analogs was evaluated on Cytotoxicity and mechanisms of action. This review provides a comprehensive overview of the cytotoxicity and mechanisms of action of anticancer-active organoiridium(III) complexes with Schiff base and oxime ligands.
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