Catadegbrutinib (BGB-16673) is a potent inhibitor of BTK (0.69 ± 0.091 nM), CRBN-DBB1 complex (316 ± 82 nM). Catadegbrutinib (BGB-16673) exhibits the greatest inhibitory potency toward BTK (IC50 = 0.69 ± 0.091 nM).
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