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Results and Discussion Design and Synthesis of a PCa-Targeting MZ1 Prodrug Library The highly potent BET family (BRD2, 3, and 4) degrader MZ1 , a well-established but widely toxic PROTAC, was chosen as the basis of a model system to explore GSH-controlled delivery to PCa

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It pairs the strongest weight-loss peptide in current clinical development with the most established growth-hormone (GH) peptide combination