Journal of Drug Delivery Science and Technology, Journal Year: 2024, Volume and Issue: unknown, P. 106596 - 106596
Published: Dec. 1, 2024
Language: Английский
Journal of Drug Delivery Science and Technology, Journal Year: 2024, Volume and Issue: unknown, P. 106596 - 106596
Published: Dec. 1, 2024
Language: Английский
Bioanalysis, Journal Year: 2025, Volume and Issue: unknown, P. 1 - 16
Published: Feb. 3, 2025
Undruggable targets account for roughly 85% of human disease-related and represent a category therapeutic that are difficult to tackle with traditional methods, but their considerable clinical importance. These generally defined by planar functional interfaces the absence efficient ligand-binding pockets, making them unattainable conventional pharmaceutical strategies. The advent oligonucleotide-based proteolysis-targeting chimeras (PROTACs) has instilled renewed optimism in addressing these challenges. PROTACs facilitate targeted degradation undruggable entities, including transcription factors (TFs) RNA-binding proteins (RBPs), via proteasome-dependent mechanisms, thereby presenting novel approaches diseases linked targets. This review offers an in-depth examination recent progress integration PROTAC technology oligonucleotides target traditionally proteins, emphasizing design principles mechanisms action innovative PROTACs.
Language: Английский
Citations
1Journal of Drug Delivery Science and Technology, Journal Year: 2024, Volume and Issue: unknown, P. 106596 - 106596
Published: Dec. 1, 2024
Language: Английский
Citations
0