SB1317

937270-47-8

C23H24N4O

DMSO : 26.5 mg/mL (71.15 mM; Need ultrasonic and warming)

Cell Cycle/DNA Damage; Protein Tyrosine Kinase/RTK; Epigenetics; Stem Cell/Wnt; JAK/STAT Signaling

SB1317 is a potent inhibitor of CDK2, JAK2, and FLT3 for the treatment of cancer, with IC₅₀ of 13, 73, and 56 nM for CDK2, JAK2 and FLT3, respectively. IC50 & Target: IC50: 13 nM (CDK2), 73 nM (JAK2), 56 nM (FLT3)^[1] In Vitro: SB1317 has a highly novel kinase inhibitory spectrum inhibiting 17 kinases from a panel of 63, 11 of which are CDK/JAK/FLT family members. The others, Lck, Fyn, Fms, TYRO3, ERK5, and p38delta, are implicated in inflammatory and proliferative processes. Human CYP1A2, 3A4, 2C9, and 2C19 isoforms are not inhibited by SB1317 at the highest tested concentration of 25 uM, but SB1317 inhibits CYP2D6 with IC₅₀=0.95 uM, approximately at the plasma C_max observed at the maximum tolerated dose. SB1317 inhibits cell proliferation concentrations in HCT-116 (IC₅₀=0.079 uM) and HL-60 (IC₅₀=0.059 uM)^[1]. SB1317 is a novel small molecule potent CDK/JAK2/FLT3 inhibitor. SB1317 is mainly metabolized by CYP3A4 and CY1A2 in vitro. SB1317 does not inhibit any of the major human CYPs in vitro except CYP2D6 (IC₅₀=1 uM). SB1317 does not significantly induce CYP1A and CYP3A4 in human hepatocytes in vitro^[2]. In Vivo: Treatment with SB1317 at 75 mg/kg po q.d. 3x/week significantly inhibits the growth of tumors with a mean TGI of 82%, while the lower dose of 50 mg/kg po 3x/week is marginally effective. Treatment with SB1317 using either regime significantly inhibits the growth of tumors with mean TGIs of 42% and 63% for the oral and ip delivery methods, respectively^[1]. In pharmacokinetic studies SB1317 shows moderate to high systemic clearance (relative to liver blood flow), high volume of distribution (>0.6 L/kg), oral bioavailability of 24%, ca.4 and 37% in mice, rats and dogs, respectively; and extensive tissue distribution in mice^[2].