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- W4307030483 abstract "Front Cover. Proteolysis targeting chimeras (PROTACs) have emerged as a powerful technology for the degradation of disease-related proteins by the hijacking of the endogenous ubiquitin-proteasome system. A multitude of bifunctional PROTACs have been developed using small-molecule ligands; one ligand binds to the target protein of interest and one ligand binds to an E3 ligase. The characteristics of those PROTACs vary, including their reversible or irreversible covalent binding to the target protein, their binding to orthosteric and allosteric sites, their agonist or antagonist activity, and their use of multiple ligands, such as oligopeptides and nucleotides. This review introduces the mechanisms and behavior of small-molecule based PROTACs as well as targeted proteolysis techniques using peptides and nucleic acids as targeting ligands, as reported by H. Yokoo and Y. Demizu et al. in their review at 10.1002/cbdv.202200828." @default.
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- W4307030483 date "2022-10-21" @default.
- W4307030483 modified "2023-09-26" @default.
- W4307030483 title "Front Cover: Recent Advances in PROTAC Technology Toward New Therapeutic Modalities (Chem. Biodiversity 11/2022)" @default.
- W4307030483 doi "https://doi.org/10.1002/cbdv.202200987" @default.
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