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Recent advances in developing targeted protein degraders.
- Source :
-
European journal of medicinal chemistry [Eur J Med Chem] 2025 Feb 15; Vol. 284, pp. 117212. Date of Electronic Publication: 2024 Dec 27. - Publication Year :
- 2025
-
Abstract
- Targeted protein degradation (TPD) represents a promising therapeutic approach, encompassing several innovative strategies, including but not limited to proteolysis targeting chimeras (PROTACs), molecular glues, hydrophobic tag tethering degraders (HyTTD), and lysosome-targeted chimeras (LYTACs). Central to TPD are small molecule ligands, which play a critical role in mediating the degradation of target proteins. This review summarizes the current landscape of small molecule ligands for TPD molecules. These small molecule ligands can utilize the proteasome, lysosome, autophagy, or hydrophobic-tagging system to achieve the degradation of target proteins. The article mainly focuses on introducing their design principles, application advantages, and potential limitations. A brief discussion on the development prospects and future directions of TPD technology was also provided.<br />Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (Copyright © 2024 Elsevier Masson SAS. All rights reserved.)
- Subjects :
- Humans
Ligands
Proteins metabolism
Proteins chemistry
Proteins antagonists & inhibitors
Small Molecule Libraries chemistry
Small Molecule Libraries pharmacology
Small Molecule Libraries chemical synthesis
Lysosomes metabolism
Molecular Structure
Animals
Proteasome Endopeptidase Complex metabolism
Proteolysis drug effects
Subjects
Details
- Language :
- English
- ISSN :
- 1768-3254
- Volume :
- 284
- Database :
- MEDLINE
- Journal :
- European journal of medicinal chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 39736199
- Full Text :
- https://doi.org/10.1016/j.ejmech.2024.117212