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This TYR-catalyzed PROTAC design facilitates the in-situ cross-linking of two small molecules for targeted protein elimination, bypassing the need for prior covalent conjugation and mitigating issues of large molecular weights and unfavorable pharmacological properties of traditional PROTAC design

This is a common strategy in medicine, using a safer agent to reduce dependence on a riskier one, but it requires careful monitoring to ensure disease control is maintained

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These products are cleaved into glutamine, cysteine, and glycine under the action of 5-oxoalaninase and Cys-Gly peptidase, respectively, and then added to new GSH synthesis [32, 37] (summarized in Fig

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