IKZF2 Degradation: It′s Time to Take into Account it When Designing Cereblon‐Based PROTACs

Proteolysis‐targeting chimera (PROTAC) has become a very important means of protein degradation and a new way of disease treatment. In particular, PROTACs constructed with ligands for E3 ligase cereblon account for more than 90 % of the PROTACs currently in clinical research. Notably, CRBN ligands t...

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Veröffentlicht in:Chembiochem : a European journal of chemical biology 2024-08, Vol.25 (16)
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description Proteolysis‐targeting chimera (PROTAC) has become a very important means of protein degradation and a new way of disease treatment. In particular, PROTACs constructed with ligands for E3 ligase cereblon account for more than 90 % of the PROTACs currently in clinical research. Notably, CRBN ligands themselves are a class of molecular glue compounds capable of degrading neo‐substrate proteins. Compared to the target proteins degradation, the degradation of neo‐substrates, especially IKZF2, has not received enough attention. Therefore, this review summarizes the currently published IKZF2 degraders derived from articles and patents, which are conducive to the design of PROTACs with desired IKZF2 degradation from the perspective of medicinal chemistry.
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subjects Biodegradation
Chimeras
Degradation
Ligands
Medical treatment
Proteins
Proteolysis
Substrates
Ubiquitin-protein ligase
title IKZF2 Degradation: It′s Time to Take into Account it When Designing Cereblon‐Based PROTACs
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