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F648239-10mgFGFR-IN-1 is a potent FGFR inhibitor with an IC 50 of <100 nM for FGFR1 , FGFR2 , and FGFR3 , respectively (patent US20130338134A1, example 219).Form:Solid
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F648239-5mgFGFR-IN-1 is a potent FGFR inhibitor with an IC 50 of <100 nM for FGFR1 , FGFR2 , and FGFR3 , respectively (patent US20130338134A1, example 219).Form:Solid
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F649107-10mgFGFR2-IN-2 (Compound 38) is a selective FGFR2 inhibitor with IC 50 s of 389, 29, and 758 nM for FGFR1 , FGFR2 , and FGFR3 , respectivelyForm:SolidIC50& Target:FGFR2 29 nM (IC 50 ) FGFR1 389 nM (IC 50 ) FGFR3 758 nM (IC 50 )
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F649107-25mgFGFR2-IN-2 (Compound 38) is a selective FGFR2 inhibitor with IC 50 s of 389, 29, and 758 nM for FGFR1 , FGFR2 , and FGFR3 , respectivelyForm:SolidIC50& Target:FGFR2 29 nM (IC 50 ) FGFR1 389 nM (IC 50 ) FGFR3 758 nM (IC 50 )
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F649107-50mgFGFR2-IN-2 (Compound 38) is a selective FGFR2 inhibitor with IC 50 s of 389, 29, and 758 nM for FGFR1 , FGFR2 , and FGFR3 , respectivelyForm:SolidIC50& Target:FGFR2 29 nM (IC 50 ) FGFR1 389 nM (IC 50 ) FGFR3 758 nM (IC 50 )
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F649107-5mgFGFR2-IN-2 (Compound 38) is a selective FGFR2 inhibitor with IC 50 s of 389, 29, and 758 nM for FGFR1 , FGFR2 , and FGFR3 , respectivelyForm:SolidIC50& Target:FGFR2 29 nM (IC 50 ) FGFR1 389 nM (IC 50 ) FGFR3 758 nM (IC 50 )
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F655710-1mlFGFR2-IN-2 (Compound 38) is a selective FGFR2 inhibitor with IC 50 s of 389, 29, and 758 nM for FGFR1 , FGFR2 , and FGFR3 , respectivelyIC50& Target:FGFR2 29 nM (IC 50 ) FGFR1 389 nM (IC 50 ) FGFR3 758 nM (IC 50 )
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F649421-10mgFGFR3-IN-5 is a potent and selective FGFR3 inhibitor with IC 50 values of 3, 44, and 289 nM for FGFR3 , FGFR2 , and FGFR1 , respectively. FGFR3-IN-5 can be used in research of cancerIn VitroFGFR3-IN-5 (compound 37 5 mM 1 h HEK-293 cells) inhibits
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F649421-1mgFGFR3-IN-5 is a potent and selective FGFR3 inhibitor with IC 50 values of 3, 44, and 289 nM for FGFR3 , FGFR2 , and FGFR1 , respectively. FGFR3-IN-5 can be used in research of cancerIn VitroFGFR3-IN-5 (compound 37 5 mM 1 h HEK-293 cells) inhibits
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F649421-5mgFGFR3-IN-5 is a potent and selective FGFR3 inhibitor with IC 50 values of 3, 44, and 289 nM for FGFR3 , FGFR2 , and FGFR1 , respectively. FGFR3-IN-5 can be used in research of cancerIn VitroFGFR3-IN-5 (compound 37 5 mM 1 h HEK-293 cells) inhibits
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F649982-100mgFGFR4-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
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F649982-10mgFGFR4-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