glutathione bromopyruvic acid adduct An essential difference in the reactivity of the adducts of the structurally closely related flavonoids monoHER and quercetin Bromopyruvic acid is an affinity label for cysteine residues† 3-Bromopyruvate-mediated MCT1-dependent metabolic perturbation sensitizes

3 Bromopyruvate mediated MCT1 dependent metabolic perturbation sensitizes triple negative breast cancer cells to ionizing radiation Cancer & Metabolism Springer Nature Link Glutathione Mediated Conjugation of Anticancer Drugs: An Overview of Reaction Mechanisms and Biological Significance for Drug Detoxification and Bioactivation PMC Unique Use of Alkylation for ChemoRedox Activity by a PtIV Prodrug Pathak 2016 Chemistry A European Journal Wiley Online Library glutathione bromopyruvic acid adduct Synthesis and anticancer activity of Pt(iv) prodrugs containing 3 bromopyruvic as an axial ligand Rewiring of mitochondrial metabolism in A guanine ethylthioethyl glutathione adduct as a major DNA lesion in the skin and in organs of mice exposed to sulfur mustard ScienceDirect Phase II Reactions: Glutathione Conjugation and Mercapturic Acid Formation in Pharmacokinetics and Pharmacodynamics JoVE Core

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