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Medchemexpress LLC Zelebrudomide (NX-2127) | 2416131-46-7 | C39H45N9O5 | 50 MG

Supplier: Medchemexpress LLC HY15322050MG
Zelebrudomide (NX-2127) is an orally active PROTAC degrader that targets Bruton's Tyrosine Kinase (Btk). It inhibits the proliferation of BTKC481S mutant TMD8 cells more effectively than Ibrutinib and appears as a light yellow to yellow solid. The compound has a molecular weight of 719.83.
- Targets Bruton's Tyrosine Kinase (Btk)
- Inhibits the proliferation of BTKC481S mutant TMD8 cells
- Catalyzes the degradation of Ikaros (IKZF1) and Aiolos (IKZF3)
- Stimulates T cell activation
- Increases IL-2 production in primary human T cells
- Demonstrates potent degradation of BTK in cynomolgus monkeys in vivo
- Leads to superior tumor growth inhibition in both WT TMD8 and C481S mutant xenograft models in mice
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