Rocbrutinib is an orally available, highly selective Bruton's tyrosine kinase ( BTK ) inhibitor, with an IC 50 of 0.11 nM against wild-type BTK and an IC 50 of 1.0 nM against C481S-mutated BTK . Rocbrutinib reduces the viability of leukemia cells, induces cytotoxicity and inhibits cell migration. Rocbrutinib can be used in research related to chronic lymphocytic leukemia, non-Hodgkin's lymphoma and mantle cell lymphoma.
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