BPR1J-097 Hydrochloride

C27H29ClN6O3S

DMSO : 6 mg/mL (10.85 mM; Need ultrasonic and warming)

Protein Tyrosine Kinase/RTK

BPR1J-097 Hydrochloride is a novel and potent FLT3 inhibitor with an IC₅₀ of 11?nM. IC50 & Target: IC50: 11 nM (FLT3)^[1] In Vitro: BPR1J-097 Hydrochloride is a novel and potent FLT3 inhibitor with an IC₅₀ of 11nM. Phosphorylation of all FLT3-WT, FLT3-IDT, and FLT3-D835Y are inhibited by BPR1J-097 Hydrochloride at a concentration as low as 10?nM. BPR1J-097 Hydrochloride suppresses the phosphorylation of FLT3 and STAT5 in a dose-dependent manner. The IC₅₀ values of BPR1J-097 Hydrochloride on MOLM-13 and MV4-11 cells are 21+/-7 and 46+/-14 nM, respectively. The emergence of active caspase-3 is observed in MOLM-13 cells treated with BPR1J-097 Hydrochloride at 10?nM. The effect of BPR1J-097 Hydrochloride seems to be weaker in MV4-11 cells as caspase-3 is not evident until 100?nM of BPR1J-097 Hydrochloride is applied to treat cells^[1]. In Vivo: After i.v. administration of mice with BPR1J-097 Hydrochloride at two cycles of 10 or 25?mg/kg, a clear dose-dependent anti-tumour effect is observed. Tumours in mice treated with BPR1J-097 Hydrochloride (25?mg/kg per day) stop growing. BPR1J-097 Hydrochloride (25?mg/kg) shows a significant tumour shrinkage effect on the subcutaneously growing MOLM-13 tumours in a size of >2000?mm³. BPR1J-097 Hydrochloride (10 and 25?mg/kg) also produces a dose-dependent growth reduction and shrinkage of another model using MV4-11 cells. It is noted that a prolonged disappearance of MV4-11 tumours is observed in mice treated with BPR1J-097 Hydrochloride at 25?mg/kg. There is little (3%) or no body weight loss of BPR1J-097 Hydrochloride-treated nude mice during the observation periods in these in vivo studies^[1].