Discovery of a DCAF11-dependent cyanoacrylamide-containing covalent degrader of BET-proteins
- Bioorg Med Chem Lett. 2024 Jul 15:107:129779. doi: 10.1016/j.bmcl.2024.129779.
- 1. CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria.
- 2. CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria. Electronic address: [email protected].
- 3. Department of Cell Biology, Harvard Medical School, Boston, USA.
- 4. CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria. Electronic address: [email protected].
Targeted protein degradation is mediated by small molecules that induce or stabilize protein-protein interactions between targets and the ubiquitin-proteasome machinery. Currently, there remains a need to expand the repertoire of viable E3 Ligases available for hijacking. Notably, covalent chemistry has been employed to engage a handful of E3 Ligases, including DCAF11. Here, we disclose a covalent PROTAC that enables DCAF11-dependent degradation, featuring a cyanoacrylamide warhead. Our findings underscore DCAF11 as an interesting candidate with a capacity to accommodate diverse electrophilic chemistries compatible with targeted protein degradation.
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Cat. No.Product NameDescriptionTargetResearch Area
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Research Areas: Cancer
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target: Ligands for E3 LigaseResearch Areas: Cancer
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target: PROTAC LinkersResearch Areas: Cancer