Cabozantinib (S-malate) olet 6-tetramethylanilino)acetyl)(methyl)amino)-1-piperidinyl)methyl)benzamide

6-tetramethylanilino)acetyl)(methyl)amino)-1-piperidinyl)methyl)benzamide

34)/b27-26+

in contrast with the SJSA-1 cells with viability lost at 3 μM of Nutlin-3 treatment

its dysregulation and gene rearrangements are associated with a variety of tumors

Cabozantinib (S-malate) olet 6-tetramethylanilino)acetyl)(methyl)amino)-1-piperidinyl)methyl)benzamideCabozantinib, also known as XL 184 or BMS 907351, is an orally bioavailable, small molecule receptor tyrosine kinase (RTK) inhibitor with potential antineoplastic activity. Cabozantinib strongly binds to and inhibits several tyrosine receptor kinases. Specifically, cabozantinib appears to have a strong affinity for the hepatocyte growth factor receptor (Met) and vascular endothelial growth factor receptor 2 (VEGFR2), which may result in inhibition of