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CPV-161 is a preclinical cyclic thiosulfinate derivative designed as an inhibitor of thioredoxin reductase (TrxR). Developed by researchers at the University of Puerto Rico, CPV-161 targets the active-site cysteine residues of TrxR to disrupt cellular redox homeostasis, induce oxidative stress, and inhibit cell proliferation. In preclinical in vitro screenings, CPV-161 demonstrated significant cytotoxic activity against a panel of breast cancer cell lines, including MCF-7, ZR-75-1, BT-20, MDA-MB-468, SkBr-3, BT-474, and MDA-MB-231, reducing cell growth by 74% to 94%.
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