Fibroblast growth factor (FGF) family ligands

FGFR4-IN-1 is a potent inhibiotr of FGFR4 with IC 50 of 0.7 nM.In VitroFGFR4-IN-1 significantly inhibits the proliferation of HuH-7 hepatocellular carcinoma cells with IC 50 of 7.8 nM. MCE has not independently confirmed the accuracy of these

FGFR4-IN-1 is a potent inhibiotr of FGFR4 with IC 50 of 0.7 nM.In VitroFGFR4-IN-1 significantly inhibits the proliferation of HuH-7 hepatocellular carcinoma cells with IC 50 of 7.8 nM. MCE has not independently confirmed the accuracy of these

FGFR4-IN-1 is a potent inhibiotr of FGFR4 with IC 50 of 0.7 nM.In VitroFGFR4-IN-1 significantly inhibits the proliferation of HuH-7 hepatocellular carcinoma cells with IC 50 of 7.8 nM. MCE has not independently confirmed the accuracy of these

FGFR4-IN-1 is a potent inhibiotr of FGFR4 with IC 50 of 0.7 nM.In VitroFGFR4-IN-1 significantly inhibits the proliferation of HuH-7 hepatocellular carcinoma cells with IC 50 of 7.8 nM. MCE has not independently confirmed the accuracy of these

FGFR4-IN-5 is a potent and selective covalent FGFR4 inhibitor with an IC 50 of 6.5 nM. FGFR4-IN-5 exhibits strong anti-tumor activity in vivo and can be used for hepatocellular carcinoma researchIn VivoFGFR4-IN-5 (oral gavage 10 mg/kg single dose)

FGFR4-IN-5 is a potent and selective covalent FGFR4 inhibitor with an IC 50 of 6.5 nM. FGFR4-IN-5 exhibits strong anti-tumor activity in vivo and can be used for hepatocellular carcinoma researchIn VivoFGFR4-IN-5 (oral gavage 10 mg/kg single dose)

FGFR4-IN-5 is a potent and selective covalent FGFR4 inhibitor with an IC 50 of 6.5 nM. FGFR4-IN-5 exhibits strong anti-tumor activity in vivo and can be used for hepatocellular carcinoma researchIn VivoFGFR4-IN-5 (oral gavage 10 mg/kg single dose)

Formononetin-d 3 -1 is the deuterium-labeled Formononetin ( HY-N0183 ).Appearance:SolidIn Vitro:Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the

Formononetin-d 3 -1 is the deuterium-labeled Formononetin ( HY-N0183 ).Appearance:SolidIn Vitro:Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the

Infigratinib phosphate (BGJ-398 phosphate NVP-BGJ398 phosphate) is a potent inhibitor of the FGFR family with IC 50 of 0.9 nM, 1.4 nM, 1 nM, and 60 nM for FGFR1 , FGFR2 , FGFR3 , and FGFR4 , respectively.In VitroInfigratinib phosphate inhibits

Infigratinib phosphate (BGJ-398 phosphate NVP-BGJ398 phosphate) is a potent inhibitor of the FGFR family with IC 50 of 0.9 nM, 1.4 nM, 1 nM, and 60 nM for FGFR1 , FGFR2 , FGFR3 , and FGFR4 , respectively.In VitroInfigratinib phosphate inhibits

Infigratinib phosphate (BGJ-398 phosphate NVP-BGJ398 phosphate) is a potent inhibitor of the FGFR family with IC 50 of 0.9 nM, 1.4 nM, 1 nM, and 60 nM for FGFR1 , FGFR2 , FGFR3 , and FGFR4 , respectively.In VitroInfigratinib phosphate inhibits