FRAX597

1286739-19-2

C29H28ClN7OS

H2O : < 0.1 mg/mL (insoluble); DMSO : 14.29 mg/mL (25.60 mM; Need ultrasonic)

Cytoskeleton; Cell Cycle/DNA Damage

FRAX597 is a potent group I p21-activated Kinases (PAKs) inhibitor with IC₅₀ of 8, 13 and 19 nM for PAK1, 2 and 3. IC50 & Target: IC50: 8 nM (PAK1), 13 nM (PAK2), 19 nM (PAK3), >10 uM (PAK4)^[1] In Vitro: FRAX597 is determined to be a potent, ATP-competitive inhibitor of group I PAKs (PAK 1-3), with biochemical IC₅₀ values as follows: PAK1 IC₅₀=8 nM, PAK2 IC₅₀=13 nM, PAK3 IC₅₀=19 nM. The IC₅₀ toward PAK4, a member of group II PAKs is >10 uM. At a concentration of 100 nM FRAX597 displays a significant (>80% inhibition) inhibitory capacity toward YES1 (87%), RET (82%), CSF1R (91%), TEK (87%), PAK1 (82%), and PAK2 (93%). When measured using the Kinase Glo Assay in the presence of 20 nM protein and 1 uM ATP, FRAX597 displayed an IC₅₀ value of 48 nM against wild type PAK1, while IC₅₀ values against the V342F and V342Y PAK1 mutants are higher than 3 uM and 2 uM, respectively^[1]. In Vivo: Analysis of the flux reading for the animals in the two cohorts demonstrates a significantly slower tumor growth rate in FRAX597-treated mice compared with control mice. After 14 days of treatment the animals are sacrificed and the tumors excised and weighed. FRAX597-treated cohort shows significantly lower average tumor weight compared with the control cohort (0.55 g versus 1.87 g, p=0.0001)^[1].