Compile Data Set for Download or QSAR
Report error Found 113 Enz. Inhib. hit(s) with all data for entry = 50019726
TargetSerine-protein kinase ATM(Human)
Eberhard Karls University of Tubingen

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50622405BDBM50622405(CHEMBL5408388)
Affinity DataIC50: 0.100nMAssay Description:Inhibition of ATM kinase in human A549 cells in presence of etoposide by ICW assayMore data for this Ligand-Target Pair
Ligand InfoSimilars
In Depth
Date in BDB:
12/17/2024
Entry Details
PubMed
TargetSerine-protein kinase ATM(Human)
Eberhard Karls University of Tubingen

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50622405BDBM50622405(CHEMBL5408388)
Affinity DataIC50: 0.410nMAssay Description:Inhibition of human ATM kinase using p53 as substrate by FRET assayMore data for this Ligand-Target Pair
Ligand InfoSimilars
In Depth
Date in BDB:
12/17/2024
Entry Details
PubMed
TargetSerine-protein kinase ATM(Human)
Eberhard Karls University of Tubingen

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50622403BDBM50622403(CHEMBL5429597)
Affinity DataIC50: 0.480nMAssay Description:Inhibition of human ATM kinase using p53 as substrate by FRET assayMore data for this Ligand-Target Pair
Ligand InfoSimilars
In Depth
Date in BDB:
12/17/2024
Entry Details
PubMed
TargetSerine-protein kinase ATM(Human)
Eberhard Karls University of Tubingen

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50622412BDBM50622412(CHEMBL5404153)
Affinity DataIC50: 0.560nMAssay Description:Inhibition of human ATM kinase using p53 as substrate by FRET assayMore data for this Ligand-Target Pair
Ligand InfoSimilars
In Depth
Date in BDB:
12/17/2024
Entry Details
PubMed
TargetSerine-protein kinase ATM(Human)
Eberhard Karls University of Tubingen

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50622407BDBM50622407(CHEMBL5399607)
Affinity DataIC50: 0.590nMAssay Description:Inhibition of human ATM kinase using p53 as substrate by FRET assayMore data for this Ligand-Target Pair
Ligand InfoSimilars
In Depth
Date in BDB:
12/17/2024
Entry Details
PubMed
TargetSerine-protein kinase ATM(Human)
Eberhard Karls University of Tubingen

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50622406BDBM50622406(CHEMBL5433386)
Affinity DataIC50: 0.600nMAssay Description:Inhibition of ATM kinase in human A549 cells in presence of etoposide by ICW assayMore data for this Ligand-Target Pair
Ligand InfoSimilars
In Depth
Date in BDB:
12/17/2024
Entry Details
PubMed
TargetSerine-protein kinase ATM(Human)
Eberhard Karls University of Tubingen

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50622399BDBM50622399(CHEMBL5436153)
Affinity DataIC50: 0.680nMAssay Description:Inhibition of human ATM kinase using p53 as substrate by FRET assayMore data for this Ligand-Target Pair
Ligand InfoSimilars
In Depth
Date in BDB:
12/17/2024
Entry Details
PubMed
TargetSerine-protein kinase ATM(Human)
Eberhard Karls University of Tubingen

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50622413BDBM50622413(CHEMBL5438530)
Affinity DataIC50: 0.760nMAssay Description:Inhibition of human ATM kinase using p53 as substrate by FRET assayMore data for this Ligand-Target Pair
Ligand InfoSimilars
In Depth
Date in BDB:
12/17/2024
Entry Details
PubMed
TargetSerine-protein kinase ATM(Human)
Eberhard Karls University of Tubingen

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50622404BDBM50622404(CHEMBL5399096)
Affinity DataIC50: 0.770nMAssay Description:Inhibition of human ATM kinase using p53 as substrate by FRET assayMore data for this Ligand-Target Pair
Ligand InfoSimilars
In Depth
Date in BDB:
12/17/2024
Entry Details
PubMed
TargetSerine-protein kinase ATM(Human)
Eberhard Karls University of Tubingen

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50622415BDBM50622415(CHEMBL5417382)
Affinity DataIC50: 0.850nMAssay Description:Inhibition of human ATM kinase using p53 as substrate by FRET assayMore data for this Ligand-Target Pair
Ligand InfoSimilars
In Depth
Date in BDB:
12/17/2024
Entry Details
PubMed
TargetSerine-protein kinase ATM(Human)
Eberhard Karls University of Tubingen

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 245474BDBM245474(US9428503, 1)
Affinity DataIC50: 0.900nMAssay Description:Inhibition of human ATM kinase using p53 as substrate by FRET assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/17/2024
Entry Details
PubMed
TargetSerine-protein kinase ATM(Human)
Eberhard Karls University of Tubingen

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50622416BDBM50622416(CHEMBL5437608)
Affinity DataIC50: 0.960nMAssay Description:Inhibition of human ATM kinase using p53 as substrate by FRET assayMore data for this Ligand-Target Pair
Ligand InfoSimilars
In Depth
Date in BDB:
12/17/2024
Entry Details
PubMed
TargetSerine-protein kinase ATM(Human)
Eberhard Karls University of Tubingen

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50622406BDBM50622406(CHEMBL5433386)
Affinity DataIC50: 0.960nMAssay Description:Inhibition of human ATM kinase using p53 as substrate by FRET assayMore data for this Ligand-Target Pair
Ligand InfoSimilars
In Depth
Date in BDB:
12/17/2024
Entry Details
PubMed
TargetSerine-protein kinase ATM(Human)
Eberhard Karls University of Tubingen

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50622411BDBM50622411(CHEMBL5422787)
Affinity DataIC50: 0.980nMAssay Description:Inhibition of human ATM kinase using p53 as substrate by FRET assayMore data for this Ligand-Target Pair
Ligand InfoSimilars
In Depth
Date in BDB:
12/17/2024
Entry Details
PubMed
TargetSerine-protein kinase ATM(Human)
Eberhard Karls University of Tubingen

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50622333BDBM50622333(CHEMBL5426493)
Affinity DataIC50: 1nMAssay Description:Inhibition of human ATM kinase using p53 as substrate by FRET assayMore data for this Ligand-Target Pair
Ligand InfoSimilars
In Depth
Date in BDB:
12/17/2024
Entry Details
PubMed
TargetSerine-protein kinase ATM(Human)
Eberhard Karls University of Tubingen

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50622397BDBM50622397(CHEMBL5411362)
Affinity DataIC50: 1nMAssay Description:Inhibition of human ATM kinase using p53 as substrate by FRET assayMore data for this Ligand-Target Pair
Ligand InfoSimilars
In Depth
Date in BDB:
12/17/2024
Entry Details
PubMed
TargetSerine-protein kinase ATM(Human)
Eberhard Karls University of Tubingen

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 245474BDBM245474(US9428503, 1)
Affinity DataIC50: 1nMAssay Description:Inhibition of ATM kinase in human A549 cells in presence of etoposide by ICW assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/17/2024
Entry Details
PubMed
TargetSerine-protein kinase ATM(Human)
Eberhard Karls University of Tubingen

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50622347BDBM50622347(CHEMBL5437024)
Affinity DataIC50: 1nMAssay Description:Inhibition of human ATM kinase using p53 as substrate by FRET assayMore data for this Ligand-Target Pair
Ligand InfoSimilars
In Depth
Date in BDB:
12/17/2024
Entry Details
PubMed
TargetSerine-protein kinase ATM(Human)
Eberhard Karls University of Tubingen

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50622348BDBM50622348(CHEMBL5425524)
Affinity DataIC50: 1nMAssay Description:Inhibition of human ATM kinase using p53 as substrate by FRET assayMore data for this Ligand-Target Pair
Ligand InfoSimilars
In Depth
Date in BDB:
12/17/2024
Entry Details
PubMed
TargetSerine-protein kinase ATM(Human)
Eberhard Karls University of Tubingen

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50622345BDBM50622345(CHEMBL5409243)
Affinity DataIC50: 1nMAssay Description:Inhibition of human ATM kinase using p53 as substrate by FRET assayMore data for this Ligand-Target Pair
Ligand InfoSimilars
In Depth
Date in BDB:
12/17/2024
Entry Details
PubMed
TargetSerine-protein kinase ATM(Human)
Eberhard Karls University of Tubingen

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50622351BDBM50622351(CHEMBL5412093)
Affinity DataIC50: 1nMAssay Description:Inhibition of human ATM kinase using p53 as substrate by FRET assayMore data for this Ligand-Target Pair
Ligand InfoSimilars
In Depth
Date in BDB:
12/17/2024
Entry Details
PubMed
TargetSerine-protein kinase ATM(Human)
Eberhard Karls University of Tubingen

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50622352BDBM50622352(CHEMBL5409359)
Affinity DataIC50: 1nMAssay Description:Inhibition of human ATM kinase using p53 as substrate by FRET assayMore data for this Ligand-Target Pair
Ligand InfoSimilars
In Depth
Date in BDB:
12/17/2024
Entry Details
PubMed
TargetSerine-protein kinase ATM(Human)
Eberhard Karls University of Tubingen

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50622349BDBM50622349(CHEMBL5433726)
Affinity DataIC50: 1nMAssay Description:Inhibition of human ATM kinase using p53 as substrate by FRET assayMore data for this Ligand-Target Pair
Ligand InfoSimilars
In Depth
Date in BDB:
12/17/2024
Entry Details
PubMed
TargetSerine-protein kinase ATM(Human)
Eberhard Karls University of Tubingen

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50622353BDBM50622353(CHEMBL5394441)
Affinity DataIC50: 1nMAssay Description:Inhibition of human ATM kinase using p53 as substrate by FRET assayMore data for this Ligand-Target Pair
Ligand InfoSimilars
In Depth
Date in BDB:
12/17/2024
Entry Details
PubMed
TargetSerine-protein kinase ATM(Human)
Eberhard Karls University of Tubingen

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50622386BDBM50622386(CHEMBL5394015)
Affinity DataIC50: 1nMAssay Description:Inhibition of human ATM kinase using p53 as substrate by FRET assayMore data for this Ligand-Target Pair
Ligand InfoSimilars
In Depth
Date in BDB:
12/17/2024
Entry Details
PubMed
TargetSerine-protein kinase ATM(Human)
Eberhard Karls University of Tubingen

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50622396BDBM50622396(CHEMBL5425975)
Affinity DataIC50: 1nMAssay Description:Inhibition of human ATM kinase using p53 as substrate by FRET assayMore data for this Ligand-Target Pair
Ligand InfoSimilars
In Depth
Date in BDB:
12/17/2024
Entry Details
PubMed
TargetSerine-protein kinase ATM(Human)
Eberhard Karls University of Tubingen

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50622404BDBM50622404(CHEMBL5399096)
Affinity DataIC50: 1nMAssay Description:Inhibition of ATM kinase in human A549 cells in presence of etoposide by ICW assayMore data for this Ligand-Target Pair
Ligand InfoSimilars
In Depth
Date in BDB:
12/17/2024
Entry Details
PubMed
TargetSerine-protein kinase ATM(Human)
Eberhard Karls University of Tubingen

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50622400BDBM50622400(CHEMBL5432184)
Affinity DataIC50: 1.20nMAssay Description:Inhibition of ATM kinase in human A549 cells in presence of etoposide by ICW assayMore data for this Ligand-Target Pair
Ligand InfoSimilars
In Depth
Date in BDB:
12/17/2024
Entry Details
PubMed
TargetSerine-protein kinase ATM(Human)
Eberhard Karls University of Tubingen

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50622403BDBM50622403(CHEMBL5429597)
Affinity DataIC50: 1.40nMAssay Description:Inhibition of ATM kinase in human A549 cells in presence of etoposide by ICW assayMore data for this Ligand-Target Pair
Ligand InfoSimilars
In Depth
Date in BDB:
12/17/2024
Entry Details
PubMed
TargetSerine-protein kinase ATM(Human)
Eberhard Karls University of Tubingen

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50622414BDBM50622414(CHEMBL5414690)
Affinity DataIC50: 1.5nMAssay Description:Inhibition of human ATM kinase using p53 as substrate by FRET assayMore data for this Ligand-Target Pair
Ligand InfoSimilars
In Depth
Date in BDB:
12/17/2024
Entry Details
PubMed
TargetSerine-protein kinase ATM(Human)
Eberhard Karls University of Tubingen

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50622391BDBM50622391(CHEMBL5408220)
Affinity DataIC50: 1.60nMAssay Description:Inhibition of human ATM kinase using p53 as substrate by FRET assayMore data for this Ligand-Target Pair
Ligand InfoSimilars
In Depth
Date in BDB:
12/17/2024
Entry Details
PubMed
TargetSerine-protein kinase ATM(Human)
Eberhard Karls University of Tubingen

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50622354BDBM50622354(CHEMBL5438075)
Affinity DataIC50: 2nMAssay Description:Inhibition of human ATM kinase using p53 as substrate by FRET assayMore data for this Ligand-Target Pair
Ligand InfoSimilars
In Depth
Date in BDB:
12/17/2024
Entry Details
PubMed
TargetSerine-protein kinase ATM(Human)
Eberhard Karls University of Tubingen

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50622388BDBM50622388(CHEMBL5409888)
Affinity DataIC50: 2.10nMAssay Description:Inhibition of human ATM kinase using p53 as substrate by FRET assayMore data for this Ligand-Target Pair
Ligand InfoSimilars
In Depth
Date in BDB:
12/17/2024
Entry Details
PubMed
TargetSerine-protein kinase ATM(Human)
Eberhard Karls University of Tubingen

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50622376BDBM50622376(CHEMBL5429786)
Affinity DataIC50: 2.10nMAssay Description:Inhibition of human ATM kinase using p53 as substrate by FRET assayMore data for this Ligand-Target Pair
Ligand InfoSimilars
In Depth
Date in BDB:
12/17/2024
Entry Details
PubMed
TargetSerine-protein kinase ATM(Human)
Eberhard Karls University of Tubingen

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50622375BDBM50622375(CHEMBL5413347)
Affinity DataIC50: 2.20nMAssay Description:Inhibition of human ATM kinase using p53 as substrate by FRET assayMore data for this Ligand-Target Pair
Ligand InfoSimilars
In Depth
Date in BDB:
12/17/2024
Entry Details
PubMed
TargetSerine-protein kinase ATM(Human)
Eberhard Karls University of Tubingen

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50622366BDBM50622366(CHEMBL5433108)
Affinity DataIC50: 2.30nMAssay Description:Inhibition of human ATM kinase using p53 as substrate by FRET assayMore data for this Ligand-Target Pair
Ligand InfoSimilars
In Depth
Date in BDB:
12/17/2024
Entry Details
PubMed
TargetSerine-protein kinase ATM(Human)
Eberhard Karls University of Tubingen

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50622401BDBM50622401(CHEMBL5404392)
Affinity DataIC50: 2.5nMAssay Description:Inhibition of human ATM kinase using p53 as substrate by FRET assayMore data for this Ligand-Target Pair
Ligand InfoSimilars
In Depth
Date in BDB:
12/17/2024
Entry Details
PubMed
TargetSerine-protein kinase ATM(Human)
Eberhard Karls University of Tubingen

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50622389BDBM50622389(CHEMBL5415802)
Affinity DataIC50: 2.5nMAssay Description:Inhibition of human ATM kinase using p53 as substrate by FRET assayMore data for this Ligand-Target Pair
Ligand InfoSimilars
In Depth
Date in BDB:
12/17/2024
Entry Details
PubMed
TargetSerine-protein kinase ATM(Human)
Eberhard Karls University of Tubingen

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50622377BDBM50622377(CHEMBL5399076)
Affinity DataIC50: 2.60nMAssay Description:Inhibition of human ATM kinase using p53 as substrate by FRET assayMore data for this Ligand-Target Pair
Ligand InfoSimilars
In Depth
Date in BDB:
12/17/2024
Entry Details
PubMed
TargetSerine-protein kinase ATM(Human)
Eberhard Karls University of Tubingen

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50622334BDBM50622334(CHEMBL5404077)
Affinity DataIC50: 3nMAssay Description:Inhibition of human ATM kinase using p53 as substrate by FRET assayMore data for this Ligand-Target Pair
Ligand InfoSimilars
In Depth
Date in BDB:
12/17/2024
Entry Details
PubMed
TargetSerine-protein kinase ATM(Human)
Eberhard Karls University of Tubingen

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50622346BDBM50622346(CHEMBL5403116)
Affinity DataIC50: 3nMAssay Description:Inhibition of human ATM kinase using p53 as substrate by FRET assayMore data for this Ligand-Target Pair
Ligand InfoSimilars
In Depth
Date in BDB:
12/17/2024
Entry Details
PubMed
TargetSerine-protein kinase ATM(Human)
Eberhard Karls University of Tubingen

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50622378BDBM50622378(CHEMBL5414060)
Affinity DataIC50: 3.30nMAssay Description:Inhibition of human ATM kinase using p53 as substrate by FRET assayMore data for this Ligand-Target Pair
Ligand InfoSimilars
In Depth
Date in BDB:
12/17/2024
Entry Details
PubMed
TargetSerine-protein kinase ATM(Human)
Eberhard Karls University of Tubingen

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50622390BDBM50622390(CHEMBL5408860)
Affinity DataIC50: 3.60nMAssay Description:Inhibition of human ATM kinase using p53 as substrate by FRET assayMore data for this Ligand-Target Pair
Ligand InfoSimilars
In Depth
Date in BDB:
12/17/2024
Entry Details
PubMed
TargetSerine-protein kinase ATM(Human)
Eberhard Karls University of Tubingen

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50622381BDBM50622381(CHEMBL5427491)
Affinity DataIC50: 3.90nMAssay Description:Inhibition of human ATM kinase using p53 as substrate by FRET assayMore data for this Ligand-Target Pair
Ligand InfoSimilars
In Depth
Date in BDB:
12/17/2024
Entry Details
PubMed
TargetSerine-protein kinase ATM(Human)
Eberhard Karls University of Tubingen

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50622344BDBM50622344(CHEMBL5404241)
Affinity DataIC50: 4nMAssay Description:Inhibition of human ATM kinase using p53 as substrate by FRET assayMore data for this Ligand-Target Pair
Ligand InfoSimilars
In Depth
Date in BDB:
12/17/2024
Entry Details
PubMed
TargetSerine-protein kinase ATM(Human)
Eberhard Karls University of Tubingen

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50622367BDBM50622367(CHEMBL5427404)
Affinity DataIC50: 4.40nMAssay Description:Inhibition of human ATM kinase using p53 as substrate by FRET assayMore data for this Ligand-Target Pair
Ligand InfoSimilars
In Depth
Date in BDB:
12/17/2024
Entry Details
PubMed
TargetSerine-protein kinase ATM(Human)
Eberhard Karls University of Tubingen

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50622362BDBM50622362(CHEMBL5400086)
Affinity DataIC50: 4.80nMAssay Description:Inhibition of human ATM kinase using p53 as substrate by FRET assayMore data for this Ligand-Target Pair
Ligand InfoSimilars
In Depth
Date in BDB:
12/17/2024
Entry Details
PubMed
TargetSerine-protein kinase ATM(Human)
Eberhard Karls University of Tubingen

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50622410BDBM50622410(CHEMBL5426792)
Affinity DataIC50: 5nMAssay Description:Inhibition of human ATM kinase using p53 as substrate by FRET assayMore data for this Ligand-Target Pair
Ligand InfoSimilars
In Depth
Date in BDB:
12/17/2024
Entry Details
PubMed
TargetSerine-protein kinase ATM(Human)
Eberhard Karls University of Tubingen

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50622398BDBM50622398(CHEMBL5431231)
Affinity DataIC50: 5.5nMAssay Description:Inhibition of human ATM kinase using p53 as substrate by FRET assayMore data for this Ligand-Target Pair
Ligand InfoSimilars
In Depth
Date in BDB:
12/17/2024
Entry Details
PubMed
TargetSerine-protein kinase ATM(Human)
Eberhard Karls University of Tubingen

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50622400BDBM50622400(CHEMBL5432184)
Affinity DataIC50: 6.40nMAssay Description:Inhibition of human ATM kinase using p53 as substrate by FRET assayMore data for this Ligand-Target Pair
Ligand InfoSimilars
In Depth
Date in BDB:
12/17/2024
Entry Details
PubMed
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