BDBM50313604 5'-Fluoro-1H,1'H-[2,3']biindolylidene-3,2'-dione 3-oxime::CHEMBL1077291
SMILES Fc1ccc2NC(=O)C(c2c1)c1[nH]c2ccccc2c1N=O
InChI Key InChIKey=XEIDGVAXPPRCTD-UHFFFAOYSA-N
Data 8 IC50
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 8 hits for monomerid = 50313604
TargetReceptor-type tyrosine-protein kinase FLT3(Human)
Institute of Science and Technology
Curated by ChEMBL
Institute of Science and Technology
Curated by ChEMBL
Affinity DataIC50: 15nMAssay Description:Inhibition of FLT3 by HTRF assayMore data for this Ligand-Target Pair
TargetSerine/threonine-protein kinase 17B(Human)
Korea Research Institute of Chemical Technology
Curated by ChEMBL
Korea Research Institute of Chemical Technology
Curated by ChEMBL
Affinity DataIC50: 620nMAssay Description:Inhibition of DRAK2 (unknown origin) using MRLC3 peptide as substrate incubated for 2 hrs by ADP-Glo kinase assayMore data for this Ligand-Target Pair
Affinity DataIC50: 1.27E+3nMAssay Description:Inhibition of Aurora A by HTRF assayMore data for this Ligand-Target Pair
TargetVascular endothelial growth factor receptor 2(Human)
Institute of Science and Technology
Curated by ChEMBL
Institute of Science and Technology
Curated by ChEMBL
Affinity DataIC50: 1.53E+3nMAssay Description:Inhibition of VEGFR2 by HTRF assayMore data for this Ligand-Target Pair
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of insulin receptor by HTRF assayMore data for this Ligand-Target Pair
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of EGFR by HTRF assayMore data for this Ligand-Target Pair
TargetMacrophage-stimulating protein receptor(Human)
Institute of Science and Technology
Curated by ChEMBL
Institute of Science and Technology
Curated by ChEMBL
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of Ron by HTRF assayMore data for this Ligand-Target Pair
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of Met by HTRF assayMore data for this Ligand-Target Pair
