L18I is a Bruton's tyrosine kinase ( BTK ) PROTAC degrader that targets wild-type and BTK C481 , and recruits the cereblon E3 ligase to mediate proteasomal degradation. L18I regulates the BCR , TLR , FcγR and NLRP3 inflammasome signaling pathways, inhibits the phosphorylation of PLCγ-2 , ERK1/2 and p38 , and reduces the levels of B cell activation markers CD25 , CD69 and CD86 . L18I downregulates the NF-κB , TNF and TLR signaling pathways, reduces the production of pro-inflammatory cytokines, and decreases immune cell infiltration and immune complex deposition. L18I inhibits the proliferation of BTK -expressing lymphoma cells, induces tumor regression in xenograft models, and exhibits synergistic activity when combined with inhibitors of SYK , PI3K or Lyn . L18I can be used in research related to lupus, diffuse alveolar hemorrhage and B-cell lymphoma . (Pink: Btk ligand ( HY-13036A ); Blue: Cereblon ligand ( HY-43722 ); Black: linker ( HY-41921 )).
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