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Design, Synthesis, Electrochemical, and Biological Evaluation of Fluorescent Chlorido[,'-bis(methoxy/hydroxy)salicylidene-1,2-bis(4-methoxyphenyl)ethylenediamine]iron(III) Complexes as Anticancer Agents. | LitMetric

AI Article Synopsis

Article Abstract

The impact of methoxy and hydroxyl groups at the salicylidene moiety of chlorido[,'-bis(methoxy/hydroxy)salicylidene-1,2-bis(4-methoxyphenyl)ethylenediamine]iron(III) complexes was evaluated on human MDA-MB 231 breast cancer and HL-60 leukemia cells. Methoxylated complexes (-) inhibited proliferation, migration, and metabolic activity in a concentration-dependent manner following the rank order: > > . In particular, was highly cytotoxic with an IC of 4.2 μM which was 6.6-fold lower than that of cisplatin (IC of 27.9 μM). In contrast, hydroxylated complexes - were almost inactive up to the highest concentration tested due to lack of cellular uptake. caused a dual mode of cell death, ferroptosis, and necroptosis, whereby at higher concentrations, ferroptosis was the preferred form. Ferroptotic morphology and the presence of ferrous iron and lipid reactive oxygen species proved the involvement of ferroptosis. was identified as a promising lead compound for the design of drug candidates inducing ferroptosis.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10726350PMC
http://dx.doi.org/10.1021/acs.jmedchem.3c01359DOI Listing

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