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KT474 is a proteolysis-targeting chimera (PROTAC) that drives the degradation of IL-1 receptor-associated kinase 4 (IRAK4). It induces the degradation of IRAK4 in primary mouse and rat splenocytes and isolated dog, monkey, and human peripheral blood mononuclear cells (PBMCs) with half-maximal degradation concentration (DC50) values of 4. 2. 9. 2. and 1. nM, respectively. KT474 is selective for IRAK4 over a panel of 468 kinases at 1 µM. It inhibits IL-8 release induced by R-848 (Cay-14806) in isolated human PBMCs (IC50 = 3 nM). In vivo, KT474 (30 and 100 mg/kg, p.o.) decreases ear thickness in a mouse model of psoriasis induced by imiquimod (Cay-14956).. Solulibility: Acetonitrile: Slightly soluble: 0.1-1 mg/ml: DMSO: Sparingly soluble: 1-10 mg/ml.
This website uses cookies, which are necessary for the technical operation of the website and are always set. Other cookies, which increase the usability of this website, serve for direct advertising or simplify interaction with other websites and social networks, will only be used with your consent.
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