Compile Data Set for Download or QSAR
Report error Found 27 Enz. Inhib. hit(s) with all data for entry = 50018905
TargetTyrosine-protein kinase CSK(Human)
University of Rhode Island

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50200197BDBM50200197((S)-2-amino-N-hydroxy-3-(4-hydroxyphenyl)propaneth...)
Affinity DataIC50: 2.50E+3nMAssay Description:Inhibition of CSK measured as poly-E4Y phosphorylation by acid precipitation assay in presence of 0.2 mM CoCl2More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase CSK(Human)
University of Rhode Island

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50200187BDBM50200187((S)-2-amino-N-hydroxy-3-(4-iodophenyl)propanamide ...)
Affinity DataIC50: 3.20E+3nMAssay Description:Inhibition of CSK measured as poly-E4Y phosphorylation by acid precipitation assay in presence of 0.2 mM CoCl2More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase CSK(Human)
University of Rhode Island

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50200208BDBM50200208((S)-2-amino-N-hydroxy-3-(4-isopropylphenyl)propana...)
Affinity DataIC50: 3.30E+3nMAssay Description:Inhibition of CSK measured as poly-E4Y phosphorylation by acid precipitation assay in presence of 0.2 mM CoCl2More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase CSK(Human)
University of Rhode Island

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50200190BDBM50200190((S)-2-amino-N-hydroxy-3-(2-iodophenyl)propanamide ...)
Affinity DataIC50: 3.40E+3nMAssay Description:Inhibition of CSK measured as poly-E4Y phosphorylation by acid precipitation assay in presence of 0.2 mM CoCl2More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase CSK(Human)
University of Rhode Island

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50200198BDBM50200198((S)-2-amino-N-hydroxy-3-(4-hydroxy-3,5-diiodopheny...)
Affinity DataIC50: 3.40E+3nMAssay Description:Inhibition of CSK measured as poly-E4Y phosphorylation by acid precipitation assay in presence of 0.2 mM CoCl2More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase CSK(Human)
University of Rhode Island

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50200189BDBM50200189((S)-2-amino-N-hydroxy-3-[4-(nitrophenyl)phenyl]pro...)
Affinity DataIC50: 4.90E+3nMAssay Description:Inhibition of CSK measured as poly-E4Y phosphorylation by acid precipitation assay in presence of 0.2 mM CoCl2More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase CSK(Human)
University of Rhode Island

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50200196BDBM50200196((S)-2-amino-3-(4-bromophenyl)-N-hydroxypropionamid...)
Affinity DataIC50: 5.60E+3nMAssay Description:Inhibition of CSK measured as poly-E4Y phosphorylation by acid precipitation assay in presence of 0.2 mM CoCl2More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase CSK(Human)
University of Rhode Island

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50200201BDBM50200201((S)-2-amino-N-hydroxy-3-[3-(nitrophenyl)phenyl]pro...)
Affinity DataIC50: 6.10E+3nMAssay Description:Inhibition of CSK measured as poly-E4Y phosphorylation by acid precipitation assay in presence of 0.2 mM CoCl2More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase CSK(Human)
University of Rhode Island

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50200188BDBM50200188((S)-2-amino-3-(4-chlorophenyl)-N-hydroxypropanamid...)
Affinity DataIC50: 6.30E+3nMAssay Description:Inhibition of CSK measured as poly-E4Y phosphorylation by acid precipitation assay in presence of 0.2 mM CoCl2More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase CSK(Human)
University of Rhode Island

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50200206BDBM50200206((S)-2-amino-N-hydroxy-3-(4-nitrophenyl)propanamide...)
Affinity DataIC50: 7.00E+3nMAssay Description:Inhibition of CSK measured as poly-E4Y phosphorylation by acid precipitation assay in presence of 0.2 mM CoCl2More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase CSK(Human)
University of Rhode Island

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50200203BDBM50200203((S)-2-amino-N-hydroxy-3-p-tolylpropionamide | CHEM...)
Affinity DataIC50: 9.50E+3nMAssay Description:Inhibition of CSK measured as poly-E4Y phosphorylation by acid precipitation assay in presence of 0.2 mM CoCl2More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase CSK(Human)
University of Rhode Island

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50200200BDBM50200200((S)-2-amino-N-hydroxy-3-(4-hydroxyphenyl)propanami...)
Affinity DataIC50: 9.50E+3nMAssay Description:Inhibition of CSK measured as poly-E4Y phosphorylation by acid precipitation assay in presence of 0.2 mM CoCl2More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase CSK(Human)
University of Rhode Island

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50200205BDBM50200205((S)-2-amino-3-(4-fluorophenyl)-N-hydroxypropanamid...)
Affinity DataIC50: 1.10E+4nMAssay Description:Inhibition of CSK measured as poly-E4Y phosphorylation by acid precipitation assay in presence of 0.2 mM CoCl2More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase CSK(Human)
University of Rhode Island

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50200184BDBM50200184((S)-2-amino-N-hydroxy-3-[4-(phenyl)phenyl]propanam...)
Affinity DataIC50: 1.20E+4nMAssay Description:Inhibition of CSK measured as poly-E4Y phosphorylation by acid precipitation assay in presence of 0.2 mM CoCl2More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase CSK(Human)
University of Rhode Island

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50200194BDBM50200194((S)-2-amino-N-hydroxy-3-phenylpropanamide | CHEMBL...)
Affinity DataIC50: 1.55E+4nMAssay Description:Inhibition of CSK measured as poly-E4Y phosphorylation by acid precipitation assay in presence of 0.2 mM CoCl2More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase CSK(Human)
University of Rhode Island

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50200185BDBM50200185((S)-2-amino-N-hydroxy-4-(4-hydroxyphenyl)butanamid...)
Affinity DataIC50: 1.80E+4nMAssay Description:Inhibition of CSK measured as poly-E4Y phosphorylation by acid precipitation assay in presence of 0.2 mM CoCl2More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase CSK(Human)
University of Rhode Island

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50200193BDBM50200193((S)-2-amino-3-(3,4-difluorophenyl)-N-hydroxypropan...)
Affinity DataIC50: 1.80E+4nMAssay Description:Inhibition of CSK measured as poly-E4Y phosphorylation by acid precipitation assay in presence of 0.2 mM CoCl2More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Human)
University of Rhode Island

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50200200BDBM50200200((S)-2-amino-N-hydroxy-3-(4-hydroxyphenyl)propanami...)
Affinity DataKi:  1.80E+4nMAssay Description:Inhibition of SRCMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase CSK(Human)
University of Rhode Island

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50200207BDBM50200207((S)-2-amino-3-(4-azidophenyl)-N-hydroxypropanamide...)
Affinity DataIC50: 2.10E+4nMAssay Description:Inhibition of CSK measured as poly-E4Y phosphorylation by acid precipitation assay in presence of 0.2 mM CoCl2More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase CSK(Human)
University of Rhode Island

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50200192BDBM50200192((S)-2-amino-3-(4-cyanophenyl)-N-hydroxypropanamide...)
Affinity DataIC50: 2.80E+4nMAssay Description:Inhibition of CSK measured as poly-E4Y phosphorylation by acid precipitation assay in presence of 0.2 mM CoCl2More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase CSK(Human)
University of Rhode Island

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50200195BDBM50200195((S)-2-benzylamino-N-hydroxy-3-(4-hydroxyphenyl)pro...)
Affinity DataIC50: 2.90E+4nMAssay Description:Inhibition of CSK measured as poly-E4Y phosphorylation by acid precipitation assay in presence of 0.2 mM CoCl2More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase CSK(Human)
University of Rhode Island

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50200202BDBM50200202(4-((S)-2-(hydroxycarbamoyl)-2-aminoethyl)phenylbor...)
Affinity DataIC50: 3.40E+4nMAssay Description:Inhibition of CSK measured as poly-E4Y phosphorylation by acid precipitation assay in presence of 0.2 mM CoCl2More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase CSK(Human)
University of Rhode Island

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50200204BDBM50200204((S)-2-amino-3-(4-aminophenyl)-N-hydroxypropanamide...)
Affinity DataIC50: 4.70E+4nMAssay Description:Inhibition of CSK measured as poly-E4Y phosphorylation by acid precipitation assay in presence of 0.2 mM CoCl2More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase CSK(Human)
University of Rhode Island

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50200186BDBM50200186((S)-2-amino-N-hydroxy-2-(4-hydroxyphenyl)acetamide...)
Affinity DataIC50: 5.70E+4nMAssay Description:Inhibition of CSK measured as poly-E4Y phosphorylation by acid precipitation assay in presence of 0.2 mM CoCl2More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase CSK(Human)
University of Rhode Island

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50200191BDBM50200191((S)-2-amino-3-(4-hydroxyphenyl)propanehydrazide | ...)
Affinity DataIC50: 7.50E+4nMAssay Description:Inhibition of CSK measured as poly-E4Y phosphorylation by acid precipitation assay in presence of 0.2 mM CoCl2More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase CSK(Human)
University of Rhode Island

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50200199BDBM50200199((S)-N-hydroxy-3-(4-hydroxyphenyl)-2-phenylpropanam...)
Affinity DataIC50: 2.90E+5nMAssay Description:Inhibition of CSK measured as poly-E4Y phosphorylation by acid precipitation assay in presence of 0.2 mM CoCl2More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase CSK(Human)
University of Rhode Island

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50200183BDBM50200183((S)-2-amino-N-benzyl-N-hydroxy-3-(4-hydroxyphenyl)...)
Affinity DataIC50: 2.91E+5nMAssay Description:Inhibition of CSK measured as poly-E4Y phosphorylation by acid precipitation assay in presence of 0.2 mM CoCl2More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed