Description
A dual inhibitor of FLT3 and Cdk4 (IC50s = 1 and 3 nM, respectively); selective for FLT3 and Cdk4 over Cdk1 (IC50 = 2.22 μM); also binds to FLT3ITD, FLT3D835Y, FLT3D835H, FLT3K663Q, and FLT3N841I (Kds = 1-4 nM); inhibits proliferation of MOLM-13, COLO 205, and U937 cancer cells (IC50s = 19, 55, and 52 nM, respectively); reduces intratumor levels of pSTAT5 and pRb and inhibits tumor growth in a MOLM-13 AML mouse xenograft model
Formal name: 1-[7,8-dihydro-2-[[9-(trans-4-methylcyclohexyl)-9H-pyrido[4′,3′:4,5]pyrrolo[2,3-d]pyrimidin-2-yl]amino]-1,6-naphthyridin-6(5H)-yl]-2-hydroxy-ethanone
Synonyms:
Molecular weight: 471.6
CAS: 1401033-86-0
Purity: ≥95%
Formulation: A crystalline solid