Molecular Formula | C25H25F3N4O4 |
Molar Mass | 502.49 |
Density | 1.353±0.06 g/cm3(Predicted) |
Boling Point | 601.9±55.0 °C(Predicted) |
pKa | 10.86±0.70(Predicted) |
Storage Condition | Room Temprature |
In vitro study | In a tumor model with BRAF V600 mutation, LXH254 not only inhibited MAPK signaling activity, but also inhibited mutant N-and KRAS-driven signaling. LXH254 can inhibit RAF monomer or dimer with equal efficacy. LXH254 has oral bioavailability and can cause tumor regression in a variety of cell lines and xenograft models derived from human primary tumors. |