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

Supplier:  Medchemexpress LLC HY15322050MG

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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

Catalog No. 50-003-73511


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