PROTAC ERRα Degrader-3 is a potent and selective ERRα degrader based on von Hippel-Lindau ligand. PROTAC ERRα Degrader-3 is capable of specifically degrading ERRα protein by >80% at a concentration of 30 nM. PROTAC ERRα Degrader-3 is inactive against ERRβ and ERRγ proteins In Vitro PROTAC ERRα Degrader-3 (compound 6c; 0.3 nM-10 μM; 4 hours) dose-dependently induces ERRα degradation with an efficacious dose as low as 3.0 nM at 4.0 h. PROTAC ERRα Degrader-3 potently decreases protein levels of ERRα downstream target genes, e.g., ATP5B, medium-chain acyl CoA dehydrogenase (MCAD), and pyruvate dehydrogenase kinase 4 (PDK4) in the MDA-MB-231 cells after a 24 h treatment. PROTAC ERRα Degrader-3 exhibits an IC 50 value of 12.67 nM to block the protein-protein interaction of ERRα with PGC-1α peptide and induces approximately 96% protein degradation at 100 nM (D100 nM) after 4.0 h treatment. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Western Blot AnalysisCell Line: MDA-MB-231 cells Concentration: 0.3 nM, 1 nM, 3 nM, 10 nM, 30 nM, 100 nM, 300 nM, 1 μM, 3 μM, 10 μM Incubation Time: 4 hours Result: Dose-dependently induced ERRα degradation. IC50& Target:ERRα VHL
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PROTAC ERRα Degrader-3
CAS number:2306388-65-6(DMSO) molecular formula:C47H50F6N6O7S
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| Chinese alias | PROTAC ERRα 降解剂-3 | ||
| English alias | - | ||
| CAS number | 2306388-65-6(DMSO) | molecular formula | C47H50F6N6O7S |
| molecular weight | 956.99 g/mol | Exact mass | 10mM in DMSO |
| PSA | - | logp | - |
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