FGFR3-IN-5 is a potent and selective cancer[1].
FGFR3-IN-5 (compound 37; 5 mM; 1 h; HEK-293 细胞) 抑制 FGFR 磷酸化,对 FGFR3 和 FGFR1 的 IC50 值分别为8 nM 和 59 nM[1]。
[1]. James FB, et, al. Substituted pyrazolo[1,5-a]pyridine compounds as inhibitors of fgfr tyrosine kinases. WO2020131627.
















