Compile Data Set for Download or QSAR
Report error Found 56 Enz. Inhib. hit(s) with all data for entry = 4970
TargetCyclin-dependent kinase 2(Human)
Schering

LigandChemical structure of BindingDB Monomer ID 84541BDBM84541(Indirubin derivative, 22)
Affinity DataIC50: 10nMpH: 8.0 T: 2°CAssay Description:Inhibition assay using CDK and selective kinases such as gsk3, EGFR, c-Kit, InsR and KDR.More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/16/2012
Entry Details Article
PubMed
TargetCyclin-dependent kinase 2(Human)
Schering

LigandChemical structure of BindingDB Monomer ID 84539BDBM84539(Indirubin derivative, 36 (X=O))
Affinity DataIC50: 20nMpH: 8.0 T: 2°CAssay Description:Inhibition assay using CDK and selective kinases such as gsk3, EGFR, c-Kit, InsR and KDR.More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/16/2012
Entry Details Article
PubMed
TargetCyclin-dependent kinase 2(Human)
Schering

LigandChemical structure of BindingDB Monomer ID 84535BDBM84535(Indirubin derivative, 8)
Affinity DataIC50: 40nMpH: 8.0 T: 2°CAssay Description:Inhibition assay using CDK and selective kinases such as gsk3, EGFR, c-Kit, InsR and KDR.More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/16/2012
Entry Details Article
PubMed
TargetCyclin-dependent kinase 2(Human)
Schering

LigandChemical structure of BindingDB Monomer ID 84536BDBM84536(Indirubin derivative, 32)
Affinity DataIC50: 40nMpH: 8.0 T: 2°CAssay Description:Inhibition assay using CDK and selective kinases such as gsk3, EGFR, c-Kit, InsR and KDR.More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/16/2012
Entry Details Article
PubMed
TargetCyclin-dependent kinase 2(Human)
Schering

LigandChemical structure of BindingDB Monomer ID 84555BDBM84555(Indirubin derivative, 30b | Indirubin derivative, ...)
Affinity DataIC50: 40nMpH: 8.0 T: 2°CAssay Description:Inhibition assay using CDK and selective kinases such as gsk3, EGFR, c-Kit, InsR and KDR.More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/16/2012
Entry Details Article
PubMed
TargetCyclin-dependent kinase 2(Human)
Schering

LigandChemical structure of BindingDB Monomer ID 84542BDBM84542(Indirubin derivative, 23)
Affinity DataIC50: 40nMpH: 8.0 T: 2°CAssay Description:Inhibition assay using CDK and selective kinases such as gsk3, EGFR, c-Kit, InsR and KDR.More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/16/2012
Entry Details Article
PubMed
TargetCyclin-dependent kinase 2(Human)
Schering

LigandChemical structure of BindingDB Monomer ID 84553BDBM84553(Indirubin derivative, 28b | Indirubin derivative, ...)
Affinity DataIC50: 70nMpH: 8.0 T: 2°CAssay Description:Inhibition assay using CDK and selective kinases such as gsk3, EGFR, c-Kit, InsR and KDR.More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/16/2012
Entry Details Article
PubMed
TargetCyclin-dependent kinase 2(Human)
Schering

LigandChemical structure of BindingDB Monomer ID 84546BDBM84546(Indirubin derivative, 27b | Indirubin derivative, ...)
Affinity DataIC50: 70nMpH: 8.0 T: 2°CAssay Description:Inhibition assay using CDK and selective kinases such as gsk3, EGFR, c-Kit, InsR and KDR.More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/16/2012
Entry Details Article
PubMed
TargetCyclin-dependent kinase 2(Human)
Schering

LigandChemical structure of BindingDB Monomer ID 84537BDBM84537(Indirubin derivative, 33)
Affinity DataIC50: 80nMpH: 8.0 T: 2°CAssay Description:Inhibition assay using CDK and selective kinases such as gsk3, EGFR, c-Kit, InsR and KDR.More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/16/2012
Entry Details Article
PubMed
TargetCyclin-dependent kinase 2(Human)
Schering

LigandChemical structure of BindingDB Monomer ID 84544BDBM84544(Indirubin derivative, 36 (X=NO))
Affinity DataIC50: 80nMpH: 8.0 T: 2°CAssay Description:Inhibition assay using CDK and selective kinases such as gsk3, EGFR, c-Kit, InsR and KDR.More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/16/2012
Entry Details Article
PubMed
TargetCyclin-dependent kinase 2(Human)
Schering

LigandChemical structure of BindingDB Monomer ID 54680BDBM54680(cid_5287845 | UNM-0000305770 | (3Z)-5-bromanyl-3-(...)
Affinity DataIC50: 80nMpH: 8.0 T: 2°CAssay Description:Inhibition assay using CDK and selective kinases such as gsk3, EGFR, c-Kit, InsR and KDR.More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/16/2012
Entry Details Article
PubMed
TargetCyclin-dependent kinase 2(Human)
Schering

LigandChemical structure of BindingDB Monomer ID 84543BDBM84543(Indirubin derivative, 25)
Affinity DataIC50: 90nMpH: 8.0 T: 2°CAssay Description:Inhibition assay using CDK and selective kinases such as gsk3, EGFR, c-Kit, InsR and KDR.More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/16/2012
Entry Details Article
PubMed
TargetCyclin-dependent kinase 2(Human)
Schering

LigandChemical structure of BindingDB Monomer ID 84548BDBM84548(Indirubin derivative, 29b | Indirubin derivative, ...)
Affinity DataIC50: 90nMpH: 8.0 T: 2°CAssay Description:Inhibition assay using CDK and selective kinases such as gsk3, EGFR, c-Kit, InsR and KDR.More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/16/2012
Entry Details Article
PubMed
TargetCyclin-dependent kinase 2(Human)
Schering

LigandChemical structure of BindingDB Monomer ID 84534BDBM84534(Indirubin derivative, 20)
Affinity DataIC50: 300nMpH: 8.0 T: 2°CAssay Description:Inhibition assay using CDK and selective kinases such as gsk3, EGFR, c-Kit, InsR and KDR.More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/16/2012
Entry Details Article
PubMed
TargetCyclin-dependent kinase 2(Human)
Schering

LigandChemical structure of BindingDB Monomer ID 84553BDBM84553(Indirubin derivative, 28b | Indirubin derivative, ...)
Affinity DataIC50: 400nMpH: 8.0 T: 2°CAssay Description:Inhibition assay using CDK and selective kinases such as gsk3, EGFR, c-Kit, InsR and KDR.More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/16/2012
Entry Details Article
PubMed
TargetCyclin-dependent kinase 2(Human)
Schering

LigandChemical structure of BindingDB Monomer ID 84540BDBM84540(Indirubin derivative, 35)
Affinity DataIC50: 450nMpH: 8.0 T: 2°CAssay Description:Inhibition assay using CDK and selective kinases such as gsk3, EGFR, c-Kit, InsR and KDR.More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/16/2012
Entry Details Article
PubMed
TargetCyclin-dependent kinase 2(Human)
Schering

LigandChemical structure of BindingDB Monomer ID 84534BDBM84534(Indirubin derivative, 20)
Affinity DataIC50: 500nMpH: 8.0 T: 2°CAssay Description:Inhibition assay using CDK and selective kinases such as gsk3, EGFR, c-Kit, InsR and KDR.More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/16/2012
Entry Details Article
PubMed
TargetCyclin-dependent kinase 2(Human)
Schering

LigandChemical structure of BindingDB Monomer ID 84555BDBM84555(Indirubin derivative, 30b | Indirubin derivative, ...)
Affinity DataIC50: 600nMpH: 8.0 T: 2°CAssay Description:Inhibition assay using CDK and selective kinases such as gsk3, EGFR, c-Kit, InsR and KDR.More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/16/2012
Entry Details Article
PubMed
TargetCyclin-dependent kinase 2(Human)
Schering

LigandChemical structure of BindingDB Monomer ID 84546BDBM84546(Indirubin derivative, 27b | Indirubin derivative, ...)
Affinity DataIC50: 600nMpH: 8.0 T: 2°CAssay Description:Inhibition assay using CDK and selective kinases such as gsk3, EGFR, c-Kit, InsR and KDR.More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/16/2012
Entry Details Article
PubMed
TargetCyclin-dependent kinase 2(Human)
Schering

LigandChemical structure of BindingDB Monomer ID 54680BDBM54680(cid_5287845 | UNM-0000305770 | (3Z)-5-bromanyl-3-(...)
Affinity DataIC50: 1.00E+3nMpH: 8.0 T: 2°CAssay Description:Inhibition assay using CDK and selective kinases such as gsk3, EGFR, c-Kit, InsR and KDR.More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/16/2012
Entry Details Article
PubMed
TargetCyclin-dependent kinase 2(Human)
Schering

LigandChemical structure of BindingDB Monomer ID 84538BDBM84538(Indirubin derivative, 34)
Affinity DataIC50: 1.50E+3nMpH: 8.0 T: 2°CAssay Description:Inhibition assay using CDK and selective kinases such as gsk3, EGFR, c-Kit, InsR and KDR.More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/16/2012
Entry Details Article
PubMed
TargetCyclin-dependent kinase 2(Human)
Schering

LigandChemical structure of BindingDB Monomer ID 84552BDBM84552(Indirubin derivative, 37)
Affinity DataIC50: 1.60E+3nMpH: 8.0 T: 2°CAssay Description:Inhibition assay using CDK and selective kinases such as gsk3, EGFR, c-Kit, InsR and KDR.More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/16/2012
Entry Details Article
PubMed
TargetCyclin-dependent kinase 2(Human)
Schering

LigandChemical structure of BindingDB Monomer ID 7392BDBM7392(2-[(3Z)-2-oxo-2,3-dihydro-1H-indol-3-ylidene]-2,3-...)
Affinity DataIC50: 2.00E+3nMpH: 8.0 T: 2°CAssay Description:Inhibition assay using CDK and selective kinases such as gsk3, EGFR, c-Kit, InsR and KDR.More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/16/2012
Entry Details Article
PubMed
TargetCyclin-dependent kinase 2(Human)
Schering

LigandChemical structure of BindingDB Monomer ID 84550BDBM84550(Indirubin derivative, 31b | Indirubin derivative, ...)
Affinity DataIC50: 3.00E+3nMpH: 8.0 T: 2°CAssay Description:Inhibition assay using CDK and selective kinases such as gsk3, EGFR, c-Kit, InsR and KDR.More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/16/2012
Entry Details Article
PubMed
TargetCyclin-dependent kinase 2(Human)
Schering

LigandChemical structure of BindingDB Monomer ID 84545BDBM84545(Indirubin derivative, 26)
Affinity DataIC50: 3.00E+3nMpH: 8.0 T: 2°CAssay Description:Inhibition assay using CDK and selective kinases such as gsk3, EGFR, c-Kit, InsR and KDR.More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/16/2012
Entry Details Article
PubMed
TargetCyclin-dependent kinase 2(Human)
Schering

LigandChemical structure of BindingDB Monomer ID 84548BDBM84548(Indirubin derivative, 29b | Indirubin derivative, ...)
Affinity DataIC50: 4.00E+3nMpH: 8.0 T: 2°CAssay Description:Inhibition assay using CDK and selective kinases such as gsk3, EGFR, c-Kit, InsR and KDR.More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/16/2012
Entry Details Article
PubMed
TargetCyclin-dependent kinase 2(Human)
Schering

LigandChemical structure of BindingDB Monomer ID 84536BDBM84536(Indirubin derivative, 32)
Affinity DataIC50: 4.00E+3nMpH: 8.0 T: 2°CAssay Description:Inhibition assay using CDK and selective kinases such as gsk3, EGFR, c-Kit, InsR and KDR.More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/16/2012
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 84534BDBM84534(Indirubin derivative, 20)
Affinity DataIC50: 1.00E+4nMpH: 7.0 T: 2°CAssay Description:Inhibition assay using CDK and selective kinases such as gsk3, EGFR, c-Kit, InsR and KDR.More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/16/2012
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 84553BDBM84553(Indirubin derivative, 28b | Indirubin derivative, ...)
Affinity DataIC50: 1.00E+4nMpH: 7.0 T: 2°CAssay Description:Inhibition assay using CDK and selective kinases such as gsk3, EGFR, c-Kit, InsR and KDR.More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/16/2012
Entry Details Article
PubMed
TargetKit ligand(Human)
Schering

LigandChemical structure of BindingDB Monomer ID 84555BDBM84555(Indirubin derivative, 30b | Indirubin derivative, ...)
Affinity DataIC50: 1.00E+4nMpH: 7.0 T: 2°CAssay Description:Inhibition assay using CDK and selective kinases such as gsk3, EGFR, c-Kit, InsR and KDR.More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/16/2012
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 54680BDBM54680(cid_5287845 | UNM-0000305770 | (3Z)-5-bromanyl-3-(...)
Affinity DataIC50: 1.00E+4nMpH: 7.0 T: 2°CAssay Description:Inhibition assay using CDK and selective kinases such as gsk3, EGFR, c-Kit, InsR and KDR.More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/16/2012
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 84555BDBM84555(Indirubin derivative, 30b | Indirubin derivative, ...)
Affinity DataIC50: 1.00E+4nMpH: 7.0 T: 2°CAssay Description:Inhibition assay using CDK and selective kinases such as gsk3, EGFR, c-Kit, InsR and KDR.More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/16/2012
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 84553BDBM84553(Indirubin derivative, 28b | Indirubin derivative, ...)
Affinity DataIC50: 1.00E+4nMpH: 7.0 T: 2°CAssay Description:Inhibition assay using CDK and selective kinases such as gsk3, EGFR, c-Kit, InsR and KDR.More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/16/2012
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 84555BDBM84555(Indirubin derivative, 30b | Indirubin derivative, ...)
Affinity DataIC50: 1.00E+4nMpH: 7.0 T: 2°CAssay Description:Inhibition assay using CDK and selective kinases such as gsk3, EGFR, c-Kit, InsR and KDR.More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/16/2012
Entry Details Article
PubMed
TargetCyclin-dependent kinase 2(Human)
Schering

LigandChemical structure of BindingDB Monomer ID 84550BDBM84550(Indirubin derivative, 31b | Indirubin derivative, ...)
Affinity DataIC50: 1.00E+4nMpH: 8.0 T: 2°CAssay Description:Inhibition assay using CDK and selective kinases such as gsk3, EGFR, c-Kit, InsR and KDR.More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/16/2012
Entry Details Article
PubMed
TargetCyclin-dependent kinase 2(Human)
Schering

LigandChemical structure of BindingDB Monomer ID 84553BDBM84553(Indirubin derivative, 28b | Indirubin derivative, ...)
Affinity DataIC50: 1.00E+4nMpH: 8.0 T: 2°CAssay Description:Inhibition assay using CDK and selective kinases such as gsk3, EGFR, c-Kit, InsR and KDR.More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/16/2012
Entry Details Article
PubMed
TargetCyclin-dependent kinase 2(Human)
Schering

LigandChemical structure of BindingDB Monomer ID 84555BDBM84555(Indirubin derivative, 30b | Indirubin derivative, ...)
Affinity DataIC50: 1.00E+4nMpH: 8.0 T: 2°CAssay Description:Inhibition assay using CDK and selective kinases such as gsk3, EGFR, c-Kit, InsR and KDR.More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/16/2012
Entry Details Article
PubMed
TargetInsulin receptor(Human)
Schering

LigandChemical structure of BindingDB Monomer ID 54680BDBM54680(cid_5287845 | UNM-0000305770 | (3Z)-5-bromanyl-3-(...)
Affinity DataIC50: 1.00E+4nMpH: 7.5 T: 2°CAssay Description:Inhibition assay using CDK and selective kinases such as gsk3, EGFR, c-Kit, InsR and KDR.More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/16/2012
Entry Details Article
PubMed
TargetCyclin-dependent kinase 2(Human)
Schering

LigandChemical structure of BindingDB Monomer ID 84553BDBM84553(Indirubin derivative, 28b | Indirubin derivative, ...)
Affinity DataIC50: 1.00E+4nMpH: 8.0 T: 2°CAssay Description:Inhibition assay using CDK and selective kinases such as gsk3, EGFR, c-Kit, InsR and KDR.More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/16/2012
Entry Details Article
PubMed
TargetCyclin-dependent kinase 2(Human)
Schering

LigandChemical structure of BindingDB Monomer ID 84555BDBM84555(Indirubin derivative, 30b | Indirubin derivative, ...)
Affinity DataIC50: 1.00E+4nMpH: 8.0 T: 2°CAssay Description:Inhibition assay using CDK and selective kinases such as gsk3, EGFR, c-Kit, InsR and KDR.More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/16/2012
Entry Details Article
PubMed
TargetInsulin receptor(Human)
Schering

LigandChemical structure of BindingDB Monomer ID 84553BDBM84553(Indirubin derivative, 28b | Indirubin derivative, ...)
Affinity DataIC50: 1.00E+4nMpH: 7.5 T: 2°CAssay Description:Inhibition assay using CDK and selective kinases such as gsk3, EGFR, c-Kit, InsR and KDR.More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/16/2012
Entry Details Article
PubMed
TargetInsulin receptor(Human)
Schering

LigandChemical structure of BindingDB Monomer ID 84555BDBM84555(Indirubin derivative, 30b | Indirubin derivative, ...)
Affinity DataIC50: 1.00E+4nMpH: 7.5 T: 2°CAssay Description:Inhibition assay using CDK and selective kinases such as gsk3, EGFR, c-Kit, InsR and KDR.More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/16/2012
Entry Details Article
PubMed
TargetInsulin receptor(Human)
Schering

LigandChemical structure of BindingDB Monomer ID 84534BDBM84534(Indirubin derivative, 20)
Affinity DataIC50: 1.00E+4nMpH: 7.5 T: 2°CAssay Description:Inhibition assay using CDK and selective kinases such as gsk3, EGFR, c-Kit, InsR and KDR.More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/16/2012
Entry Details Article
PubMed
TargetInsulin receptor(Human)
Schering

LigandChemical structure of BindingDB Monomer ID 84553BDBM84553(Indirubin derivative, 28b | Indirubin derivative, ...)
Affinity DataIC50: 1.00E+4nMpH: 7.5 T: 2°CAssay Description:Inhibition assay using CDK and selective kinases such as gsk3, EGFR, c-Kit, InsR and KDR.More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/16/2012
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 84534BDBM84534(Indirubin derivative, 20)
Affinity DataIC50: 1.00E+4nMpH: 7.0 T: 2°CAssay Description:Inhibition assay using CDK and selective kinases such as gsk3, EGFR, c-Kit, InsR and KDR.More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/16/2012
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 84553BDBM84553(Indirubin derivative, 28b | Indirubin derivative, ...)
Affinity DataIC50: 1.00E+4nMpH: 7.0 T: 2°CAssay Description:Inhibition assay using CDK and selective kinases such as gsk3, EGFR, c-Kit, InsR and KDR.More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/16/2012
Entry Details Article
PubMed
TargetInsulin receptor(Human)
Schering

LigandChemical structure of BindingDB Monomer ID 84555BDBM84555(Indirubin derivative, 30b | Indirubin derivative, ...)
Affinity DataIC50: 1.00E+4nMpH: 7.5 T: 2°CAssay Description:Inhibition assay using CDK and selective kinases such as gsk3, EGFR, c-Kit, InsR and KDR.More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/16/2012
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 54680BDBM54680(cid_5287845 | UNM-0000305770 | (3Z)-5-bromanyl-3-(...)
Affinity DataIC50: 1.00E+4nMpH: 7.0 T: 2°CAssay Description:Inhibition assay using CDK and selective kinases such as gsk3, EGFR, c-Kit, InsR and KDR.More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/16/2012
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 84555BDBM84555(Indirubin derivative, 30b | Indirubin derivative, ...)
Affinity DataIC50: 1.00E+4nMpH: 7.0 T: 2°CAssay Description:Inhibition assay using CDK and selective kinases such as gsk3, EGFR, c-Kit, InsR and KDR.More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/16/2012
Entry Details Article
PubMed
TargetKit ligand(Human)
Schering

LigandChemical structure of BindingDB Monomer ID 54680BDBM54680(cid_5287845 | UNM-0000305770 | (3Z)-5-bromanyl-3-(...)
Affinity DataIC50: 1.00E+4nMpH: 7.0 T: 2°CAssay Description:Inhibition assay using CDK and selective kinases such as gsk3, EGFR, c-Kit, InsR and KDR.More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/16/2012
Entry Details Article
PubMed
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