Synonyms: N-(3-(((2-((2,3-Dihydro-2-oxo-1H-indol-5-yl)amino)-5- (trifluoromethyl)-4-pyrimidinyl)amino)methyl)-2-pyridinyl)-N-methyl-methanesulfonamide benzenesulfonate; PF 562271; PF-00562271; PF-562271
Molecular Formula: C21H20F3N7O3S · C6H6O3S
Molecular Weight: 665.66
Linear Structural Formula: C21H20F3N7O3S · C6H6O3S
MDL Number: MFCD14105612
Purity: >=98% (HPLC)
Storage: 2-8C
Biochem Physiol Actions: PF-562,271 is a potent, ATP-competitive, reversible and selective inhibitor of FAK and Pyk2. PF-562,271 inhibits FAK phosphorylation in vivo.
Legal Information: Sold for research purposes under agreement from Pfizer Inc.