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I647582-5mgIDH1 Inhibitor 1 is a potent, orally bioavailable, brain-penetrant and selective mutant IDH1 inhibitor with IC 50 s of 0.021 μM, 0.045 μM, and 2.52 μM for IDH1 R132H , IDH1 R132C , and IDH1 WT , respectively Anticancer activityIn VitroIDH1
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I647011-1mgIDH1 Inhibitor 2 (compound 13) is a potent wild-type IDH1 inhibitor via a direct covalent modification of His315, with an IC 50 of 110 nMForm:SolidIC50&: Target:IDH1.
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I650783-10mgIDH1 Inhibitor 7 (Compound 88) is an IDH1 inhibitor with an IC 50 of less than 100 nMForm:SolidIC50&: Target:IDH1 <:100 nM (IC 50 ).
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I650783-25mgIDH1 Inhibitor 7 (Compound 88) is an IDH1 inhibitor with an IC 50 of less than 100 nMForm:SolidIC50&: Target:IDH1 <:100 nM (IC 50 ).
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I650783-5mgIDH1 Inhibitor 7 (Compound 88) is an IDH1 inhibitor with an IC 50 of less than 100 nMForm:SolidIC50&: Target:IDH1 <:100 nM (IC 50 ).
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I649015-1mgIDH1 Inhibitor 7-d 2 is the deuterium labeled IDH1 Inhibitor 7 ( HY-150238 ). IDH1 Inhibitor 7 is an IDH1 inhibitor with an IC 50 of less than 100 nM.In VitroStable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into
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I650995-100mgIDH889 is an orally available, brain penetrant, allosteric and mutant specific inhibitor of isocitrate dehydrogenase 1 (IDH1) . IDH889 has potent selectivity for IDH1 R132* mutations, with IC 50 s of 0.02 μM, 0.072 μM and 1.38 μM for IDH1 R132H ,
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I650995-10mgIDH889 is an orally available, brain penetrant, allosteric and mutant specific inhibitor of isocitrate dehydrogenase 1 (IDH1) . IDH889 has potent selectivity for IDH1 R132* mutations, with IC 50 s of 0.02 μM, 0.072 μM and 1.38 μM for IDH1 R132H ,
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I650995-1mgIDH889 is an orally available, brain penetrant, allosteric and mutant specific inhibitor of isocitrate dehydrogenase 1 (IDH1) . IDH889 has potent selectivity for IDH1 R132* mutations, with IC 50 s of 0.02 μM, 0.072 μM and 1.38 μM for IDH1 R132H ,
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I650995-25mgIDH889 is an orally available, brain penetrant, allosteric and mutant specific inhibitor of isocitrate dehydrogenase 1 (IDH1) . IDH889 has potent selectivity for IDH1 R132* mutations, with IC 50 s of 0.02 μM, 0.072 μM and 1.38 μM for IDH1 R132H ,
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I650995-50mgIDH889 is an orally available, brain penetrant, allosteric and mutant specific inhibitor of isocitrate dehydrogenase 1 (IDH1) . IDH889 has potent selectivity for IDH1 R132* mutations, with IC 50 s of 0.02 μM, 0.072 μM and 1.38 μM for IDH1 R132H ,
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I650995-5mgIDH889 is an orally available, brain penetrant, allosteric and mutant specific inhibitor of isocitrate dehydrogenase 1 (IDH1) . IDH889 has potent selectivity for IDH1 R132* mutations, with IC 50 s of 0.02 μM, 0.072 μM and 1.38 μM for IDH1 R132H ,