We report here strategic functionalization of the FDA approved chelator deferasirox (1) in an effort to produce organelle-targeting iron chelators with enhanced activity against A549 lung cancer cells. Derivative 8 was found to have improved antiproliferative activity relative to 1. Fluorescent cell imaging revealed that compound 8 preferentially localises within the lysosome.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8456774PMC
http://dx.doi.org/10.1039/d0cc08156fDOI Listing

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