Ibrutinib -MPEA is an orally active, blood-brain barrier permeable inhibitor of BTK and STAT5 . As a derivative of Ibrutinib ( HY-10997 ) conjugated with a PROTAC linker , Ibrutinib -MPEA allows the synthesis of a series of PROTAC molecules. Ibrutinib -MPEA significantly reduces the proliferation of neoplastic mast cells and primary mastocytoma cells by inducing apoptosis and inhibiting IgE -dependent histamine release. Ibrutinib -MPEA is applicable to the research of canine mast cell tumors, cerebral ischemia/reperfusion injury in diabetic mice, and neuroinflammation-related diseases.
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