BDBM50575072 BLU-111362::BLU-554::BLU111362::Fisogatinib::US20240199625, Compound BLU554::X-439161::X439161
SMILES COc1cc(OC)c(Cl)c(c1Cl)-c1ccc2nc(N[C@@H]3COCC[C@@H]3NC(=O)C=C)ncc2c1
InChI Key InChIKey=MGZKYOAQVGSSGC-UHFFFAOYSA-N
Data 21 IC50
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 21 hits for monomerid = 50575072
Affinity DataIC50: 2.18E+4nMAssay Description:Inhibition of CYP2B6 in human liver microsomesMore data for this Ligand-Target Pair
TargetFibroblast growth factor receptor 4(Human)
Hangzhou Apeloa Medicine Research Institute Co.
US Patent
Hangzhou Apeloa Medicine Research Institute Co.
US Patent
Affinity DataIC50: 5.98nMAssay Description:Compound preparation: Add 45 μL of DMSO to 5 μL of stock solution at a concentration of 10 mM to prepare the solution LY2874455 at 1000 M; ...More data for this Ligand-Target Pair
TargetFibroblast growth factor receptor 1(Human)
Hangzhou Apeloa Medicine Research Institute Co.
US Patent
Hangzhou Apeloa Medicine Research Institute Co.
US Patent
Affinity DataIC50: 624nMAssay Description:Compound preparation: Add 45 μL of DMSO to 5 μL of stock solution at a concentration of 10 mM to prepare the solution LY2874455 at 1000 M; ...More data for this Ligand-Target Pair
TargetFibroblast growth factor receptor 4(Human)
Hangzhou Apeloa Medicine Research Institute Co.
US Patent
Hangzhou Apeloa Medicine Research Institute Co.
US Patent
Affinity DataIC50: 5.30nMAssay Description:Inhibition of FGFR4 (unknown origin) using TK as substrate incubated for 1 hr in presence of biotin/ATP by HTRF assayMore data for this Ligand-Target Pair
TargetPotassium voltage-gated channel subfamily H member 2(Human)
Nanjing University of Chinese Medicine
Curated by ChEMBL
Nanjing University of Chinese Medicine
Curated by ChEMBL
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of hERG channel assessed as prolongation of QT interval by patch clamp methodMore data for this Ligand-Target Pair
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of CYP3A4 in human liver microsomes using testosterone as substrateMore data for this Ligand-Target Pair
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of CYP3A4 in human liver microsomes using Midazolam as substrateMore data for this Ligand-Target Pair
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of CYP2D6 in human liver microsomesMore data for this Ligand-Target Pair
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of CYP2C19 in human liver microsomesMore data for this Ligand-Target Pair
Affinity DataIC50: 2.42E+4nMAssay Description:Inhibition of CYP2C9 in human liver microsomesMore data for this Ligand-Target Pair
Affinity DataIC50: 4.70E+3nMAssay Description:Inhibition of CYP2C8 in human liver microsomesMore data for this Ligand-Target Pair
TargetFibroblast growth factor receptor 1(Human)
Hangzhou Apeloa Medicine Research Institute Co.
US Patent
Hangzhou Apeloa Medicine Research Institute Co.
US Patent
Affinity DataIC50: 624nMAssay Description:Inhibition of FGFR1 (unknown origin)More data for this Ligand-Target Pair
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of CYP1A2 in human liver microsomesMore data for this Ligand-Target Pair
TargetFibroblast growth factor receptor 4(Human)
Hangzhou Apeloa Medicine Research Institute Co.
US Patent
Hangzhou Apeloa Medicine Research Institute Co.
US Patent
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of FGFR4 V550L mutant (unknown origin) at 1 uM using Poly (Glu,Tyr) 4:1 as substrate incubated for 60 mins in presence of ATP by ELISAMore data for this Ligand-Target Pair
TargetFibroblast growth factor receptor 3(Human)
Nanjing University of Chinese Medicine
Curated by ChEMBL
Nanjing University of Chinese Medicine
Curated by ChEMBL
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of wild type FGFR3 (unknown origin) using Poly (Glu,Tyr) 4:1 as substrate incubated for 60 mins in presence of ATP by ELISAMore data for this Ligand-Target Pair
TargetFibroblast growth factor receptor 2(Human)
Nanjing University of Chinese Medicine
Curated by ChEMBL
Nanjing University of Chinese Medicine
Curated by ChEMBL
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of wild type FGFR2 (unknown origin) using Poly (Glu,Tyr) 4:1 as substrate incubated for 60 mins in presence of ATP by ELISAMore data for this Ligand-Target Pair
TargetFibroblast growth factor receptor 4(Human)
Hangzhou Apeloa Medicine Research Institute Co.
US Patent
Hangzhou Apeloa Medicine Research Institute Co.
US Patent
Affinity DataIC50: 8.80nMAssay Description:Inhibition of FGFR4 (unknown origin) using Poly (Glu,Tyr) 4:1 as substrate incubated for 60 mins in presence of ATP by ELISAMore data for this Ligand-Target Pair
TargetFibroblast growth factor receptor 1(Human)
Hangzhou Apeloa Medicine Research Institute Co.
US Patent
Hangzhou Apeloa Medicine Research Institute Co.
US Patent
Affinity DataIC50: 950nMAssay Description:Inhibition of wild type FGFR1 (unknown origin) using Poly (Glu,Tyr) 4:1 as substrate incubated for 60 mins in presence of ATP by ELISAMore data for this Ligand-Target Pair
TargetFibroblast growth factor receptor 4(Human)
Hangzhou Apeloa Medicine Research Institute Co.
US Patent
Hangzhou Apeloa Medicine Research Institute Co.
US Patent
Affinity DataIC50: 5nMAssay Description:Inhibition of FGFR4 (unknown origin)More data for this Ligand-Target Pair
TargetFibroblast growth factor receptor 3(Human)
Nanjing University of Chinese Medicine
Curated by ChEMBL
Nanjing University of Chinese Medicine
Curated by ChEMBL
Affinity DataIC50: 2.20E+3nMAssay Description:Inhibition of FGFR3 (unknown origin)More data for this Ligand-Target Pair
TargetFibroblast growth factor receptor 2(Human)
Nanjing University of Chinese Medicine
Curated by ChEMBL
Nanjing University of Chinese Medicine
Curated by ChEMBL
Affinity DataIC50: 1.20E+3nMAssay Description:Inhibition of FGFR2 (unknown origin)More data for this Ligand-Target Pair