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Retention tests on GSH-Sepharose affinity chromatography showed that, in contrast to PtGSTU20, recombinant PtGSTU19 was partially retained by the resin indicating that its GSH-binding site (G-site) is partially occupied by a molecule that is most likely GSH (Supplementary Figure S3C)

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(2005), is an additional C-terminal lysine bearing an N-3-maleimidopropionamide moiety the "drug affinity complex" (DAC) that tethers the peptide to albumin

These metabolic changes not only support the rapid proliferation of cancer cells but also enable them to survive under hostile conditions, such as nutrient deprivation and hypoxia, commonly found in the tumor microenvironment [6,7,8,9]

The mechanism involves the same AMPK activation (documented for nootkatone), induction of phase II detoxification enzymes that prevent carcinogen-DNA binding, and direct proapoptotic signaling in cancer cell lines