Description
A dual inhibitor of FAK1 (IC50s = 2.0 and 80 nM for in vitro enzyme and cellular inhibition, respectively) and ALK (IC50s = 3.1 and 22 nM for in vitro enzyme and cellular inhibition, respectively); blocks the proliferation of breast cancer cell lines in vitro or in vivo
Formal name: 2-[[5-chloro-2-[[(6S)-6,7,8,9-tetrahydro-6-[4-(2-hydroxyethyl)-1-piperazinyl]-1-methoxy-5H-benzocyclohepten-2-yl]amino]-4-pyrimidinyl]amino]-N-methyl-benzamide
Synonyms:
Molecular weight: 580.1
CAS: 1391712-60-9
Purity: ≥98%
Formulation: A crystalline solid
Product Type|Biochemicals|Kinase Inhibitors|Other Non-Receptor Tyrosine Kinases||Product Type|Biochemicals|Kinase Inhibitors|Other Receptor Tyrosine Kinases||Product Type|Biochemicals|Small Molecule Inhibitors|Kinases||Research Area|Cancer|Cell Signaling