Information provided in the product description is from published literature. Due to the nature of scientific experimentation, your results (e.g., selectivity and effective concentrations) or specific application for this product may differ. If you have questions about how this product fits your application, please contact our technical support staff.
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BAY-826 is an inhibitor of tunica interna endothelial cell kinase 2 (Tie2; IC50 = 0.5 nM).1 It inhibits Tie2 autophosphorylation in human umbilical vein endothelial cells (HUVECs; EC50 = 1.3 nM).2 BAY-826 (0.1 or 1 µM), in combination with radiation, reduces colony formation in a colony formation assay using SMA-497, SMA-540, SMA-560, and GL261 mouse glioma cells. In vivo, BAY 826 (100 mg/kg per day), in combination with radiation, decreases tumor volume and vascularization, as well as increases the number of CD45+ T cell tumor infiltrates and animal survival in an SMA-560 murine glioma model.
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1. Sustituted phenylimidazopyrazoles and their use. (2013).
2. Novel TIE-