BDBM50584948 CHEMBL5092606

SMILES CN(C)C(=O)c1ccc(Nc2ncc(c(N[C@@H]3CC[C@H](N)CC3)n2)C(F)(F)F)cc1

InChI Key InChIKey=ZFKQQXLECNVLOF-OKILXGFUSA-N

Data  18 IC50  1 EC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 19 hits for monomerid = 50584948   

TargetHigh affinity nerve growth factor receptor(Homo sapiens (Human))
Zhejiang University

Curated by ChEMBL
LigandPNGBDBM50584948(CHEMBL5092606)
Affinity DataIC50:  36nMAssay Description:Inhibition of human recombinant TRKA incubated for 1 hrs by HTRF KinEASE TK assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetReceptor-type tyrosine-protein kinase FLT3(Homo sapiens (Human))
Zhejiang University

Curated by ChEMBL
LigandPNGBDBM50584948(CHEMBL5092606)
Affinity DataIC50:  6.30nMAssay Description:Inhibition of human recombinant C terminal hFc tagged FLT3 (Asn27-Ser543 residues) expressed in HEK293 cells incubated for 1 hrs by HTRF KinEASE TKMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetInsulin-like growth factor 1 receptor(Homo sapiens (Human))
Zhejiang University

Curated by ChEMBL
LigandPNGBDBM50584948(CHEMBL5092606)
Affinity DataIC50:  1.02E+3nMAssay Description:Inhibition of human recombinant IGF1R incubated for 1 hrs by HTRF KinEASE TK assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase BTK(Homo sapiens (Human))
Zhejiang University

Curated by ChEMBL
LigandPNGBDBM50584948(CHEMBL5092606)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of human recombinant BTK incubated for 1 hrs by HTRF KinEASE TK assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase PAK 1(Homo sapiens (Human))
Zhejiang University

Curated by ChEMBL
LigandPNGBDBM50584948(CHEMBL5092606)
Affinity DataIC50:  1.28E+3nMAssay Description:Inhibition of human recombinant PAK1 incubated for 1 hrs by HTRF KinEASE TK assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAurora kinase A(Homo sapiens (Human))
Zhejiang University

Curated by ChEMBL
LigandPNGBDBM50584948(CHEMBL5092606)
Affinity DataIC50:  56nMAssay Description:Inhibition of human recombinant AURKA incubated for 1 hrs by HTRF KinEASE TK assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
Zhejiang University

Curated by ChEMBL
LigandPNGBDBM50584948(CHEMBL5092606)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of human recombinant WEE1 incubated for 1 hrs by HTRF KinEASE TK assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase JAK3(Homo sapiens (Human))
Zhejiang University

Curated by ChEMBL
LigandPNGBDBM50584948(CHEMBL5092606)
Affinity DataIC50:  333nMAssay Description:Inhibition of human recombinant JAK3 incubated for 1 hrs by HTRF KinEASE TK assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEphrin type-A receptor 1(Homo sapiens (Human))
Zhejiang University

Curated by ChEMBL
LigandPNGBDBM50584948(CHEMBL5092606)
Affinity DataIC50:  303nMAssay Description:Inhibition of human recombinant EPHA1 incubated for 1 hrs by HTRF KinEASE TK assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Zhejiang University

Curated by ChEMBL
LigandPNGBDBM50584948(CHEMBL5092606)
Affinity DataIC50:  7.14E+3nMAssay Description:Inhibition of human recombinant EGFR incubated for 1 hrs by HTRF KinEASE TK assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 2(Homo sapiens (Human))
Zhejiang University

Curated by ChEMBL
LigandPNGBDBM50584948(CHEMBL5092606)
Affinity DataIC50:  835nMAssay Description:Inhibition of human recombinant CDK2 incubated for 1 hrs by HTRF KinEASE TK assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 1(Homo sapiens (Human))
Zhejiang University

Curated by ChEMBL
LigandPNGBDBM50584948(CHEMBL5092606)
Affinity DataIC50:  1.81E+3nMAssay Description:Inhibition of human recombinant CDK1 incubated for 1 hrs by HTRF KinEASE TK assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 6(Homo sapiens (Human))
Zhejiang University

Curated by ChEMBL
LigandPNGBDBM50584948(CHEMBL5092606)
Affinity DataIC50:  1.42E+3nMAssay Description:Inhibition of human recombinant CDK6 incubated for 1 hrs by HTRF KinEASE TK assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetReceptor-type tyrosine-protein kinase FLT3(Homo sapiens (Human))
Zhejiang University

Curated by ChEMBL
LigandPNGBDBM50584948(CHEMBL5092606)
Affinity DataIC50:  7.20nMAssay Description:Inhibition of N-terminal GST tagged human recombinant wild type FLT-3 (564-993 residues) expressed in baculovirus infected Sf21 insect cells using TK...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetReceptor-type tyrosine-protein kinase FLT3(Homo sapiens (Human))
Zhejiang University

Curated by ChEMBL
LigandPNGBDBM50584948(CHEMBL5092606)
Affinity DataIC50:  5nMAssay Description:Inhibition of N-terminal GST tagged human recombinant FLT3 D835Y mutant (564 residue) expressed in baculovirus infected Sf21 insect cells using TK pe...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMast/stem cell growth factor receptor Kit(Homo sapiens (Human))
Zhejiang University

Curated by ChEMBL
LigandPNGBDBM50584948(CHEMBL5092606)
Affinity DataIC50:  7.45E+3nMAssay Description:Inhibition of N-terminal GST tagged human recombinant cKit (544 residue) expressed in baculovirus infected Sf21 insect cells using TK peptide as subs...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetALK tyrosine kinase receptor(Homo sapiens (Human))
Zhejiang University

Curated by ChEMBL
LigandPNGBDBM50584948(CHEMBL5092606)
Affinity DataIC50:  2.31E+3nMAssay Description:Inhibition of human recombinant ALK incubated for 1 hrs by HTRF KinEASE TK assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetReceptor-type tyrosine-protein kinase FLT3(Homo sapiens (Human))
Zhejiang University

Curated by ChEMBL
LigandPNGBDBM50584948(CHEMBL5092606)
Affinity DataEC50: <1nMAssay Description:Inhibition of FLT3 downstream signalling in human MV4-11 cells assessed as reduction in autophosphorylation at tyr589/591 residue for 90 mins by West...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytoplasmic tyrosine-protein kinase BMX(Homo sapiens (Human))
Zhejiang University

Curated by ChEMBL
LigandPNGBDBM50584948(CHEMBL5092606)
Affinity DataIC50:  611nMAssay Description:Inhibition of human recombinant BMX incubated for 1 hrs by HTRF KinEASE TK assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed