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.
Products | Products > Disease Areas > Cancer | Products > Disease Areas > Autoimmune Disease | Products > Disease Areas > Inflammation or Immune System Disease | Products > Signaling Pathways > PROTAC | Products > Signaling Pathways > Protein Tyrosine Kinase/RTK | Products > Signaling Pathways > Stem Cell/Wnt | Products > Signaling Pathways > JAK/STAT Signaling | Products > Research Areas > Inflammation/Immunology | Products > Research Areas > Cancer | Products > Research Areas > Cancer > Cancer Targeted Therapy | Products > Research Areas > Cancer > Cancer Immunotherapy | Products > Research Areas > Cancer > Cancer Stem Cells | Products > Signaling Pathways > Target Protein Ligand-Linker Conjugates | Products > Signaling Pathways > Btk | Products > Signaling Pathways > STAT
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