BDBM50513866 CHEMBL4450810
SMILES COc1n[nH]c2ncc(cc12)-c1cn(nn1)-c1c(F)ccc(NS(=O)(=O)c2cccc(c2)-c2ccccc2)c1F
InChI Key InChIKey=QRDCOOSKIFYKIQ-UHFFFAOYSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 12 hits for monomerid = 50513866
TargetMitogen-activated protein kinase kinase kinase 20(Homo sapiens (Human))
Jinan University
Curated by ChEMBL
Jinan University
Curated by ChEMBL
Affinity DataKd: 8nMAssay Description:Binding affinity to human ZAKMore data for this Ligand-Target Pair
Affinity DataKd: 15nMAssay Description:Binding affinity to human ABL1More data for this Ligand-Target Pair
Affinity DataKd: 190nMAssay Description:Binding affinity to human BLKMore data for this Ligand-Target Pair
Affinity DataKd: 23nMAssay Description:Binding affinity to human LIMK1More data for this Ligand-Target Pair
Affinity DataKd: 63nMAssay Description:Binding affinity to human LIMK2More data for this Ligand-Target Pair
Affinity DataKd: 160nMAssay Description:Binding affinity to human LCKMore data for this Ligand-Target Pair
TargetMitogen-activated protein kinase kinase kinase 20(Homo sapiens (Human))
Jinan University
Curated by ChEMBL
Jinan University
Curated by ChEMBL
Affinity DataKd: 8nMAssay Description:Binding affinity to ATP-binding site of human ZAK expressed in Escherichia coli by active site-dependent competition binding assayMore data for this Ligand-Target Pair
Affinity DataIC50: >1.00E+3nMAssay Description:Inhibition of recombinant human B-RAF V600E mutant using Ser/Thr3 as substrate after 1 hr by FRET-based Z'-Lyte assayMore data for this Ligand-Target Pair
TargetMitogen-activated protein kinase kinase kinase 20(Homo sapiens (Human))
Jinan University
Curated by ChEMBL
Jinan University
Curated by ChEMBL
Affinity DataIC50: 4nMAssay Description:Inhibition of N-terminal GST-tagged recombinant human full-length ZAK expressed in baculovirus infected Sf9 insect cells using MBP as substrate after...More data for this Ligand-Target Pair
TargetReceptor-type tyrosine-protein kinase FLT3(Homo sapiens (Human))
Jinan University
Curated by ChEMBL
Jinan University
Curated by ChEMBL
Affinity DataKd: 530nMAssay Description:Binding affinity to human FLT3 F691L mutantMore data for this Ligand-Target Pair
Affinity DataIC50: 156nMAssay Description:Inhibition of human ABL1More data for this Ligand-Target Pair
TargetReceptor-interacting serine/threonine-protein kinase 2(Homo sapiens (Human))
Jinan University
Curated by ChEMBL
Jinan University
Curated by ChEMBL
Affinity DataKd: 57nMAssay Description:Binding affinity to human RIPK2More data for this Ligand-Target Pair