Nunes, Joao; McGonagle, Grant A.; Eden, Jessica; Kiritharan, Girieshanie; Touzet, Megane; Lewell, Xiao; Emery, John; Eidam, Hilary; Harling, John D.; Anderson, Niall A. published the artcile< Targeting IRAK4 for Degradation with PROTACs>, Synthetic Route of 89793-12-4, the main research area is IRAK4 proteolysis targeted chimera PROTAC degradation cytokine.
Interleukin-1 Receptor-Associated Kinase 4 (IRAK4) is a key mediator of innate immunity. IRAK4 overactivation is linked with several autoimmune diseases. To date, many IRAK4 inhibitors have been developed to block the protein’s kinase activity with the most advanced reaching Phase II clin. trials. Nevertheless, several reports suggest kinase activity is not disease-relevant in certain cell types, so removing scaffolding signaling in addition to IRAK4 kinase activity may offer a better therapeutic outcome. Herein, we describe the design and synthesis of an IRAK4 Proteolysis Targeted Chimera (PROTAC). We show that IRAK4 degradation induced by compound 9 leads to the inhibition of multiple cytokines in PBMCs. However, in IL-1β stimulated human dermal fibroblasts, inhibition of IL-6 and TNF-α release was not observed despite IRAK4 degradation Nonetheless, the possibility of targeting both IRAK4 kinase and scaffolding function could potentially lead to new therapeutic opportunities to treat autoimmune, inflammatory, and oncol. diseases.
ACS Medicinal Chemistry Letters published new progress about Autoimmune disease. 89793-12-4 belongs to class pyrimidines, and the molecular formula is C7H7ClN2O2, Synthetic Route of 89793-12-4.
Referemce:
Pyrimidine | C4H4N2 – PubChem,
Pyrimidine – Wikipedia