Compile Data Set for Download or QSAR
Report error Found 19 Enz. Inhib. hit(s) with all data for entry = 834
LigandChemical structure of BindingDB Monomer ID 6469BDBM6469(4-[(4-chloro-5-methoxy-2-methylphenyl)amino]-7-met...)
Affinity DataIC50: 0.150nMpH: 7.5 T: 2°CAssay Description:Src kinase activity was measured in an ELISA format. IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the tra...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/15/2005
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 6472BDBM6472(4-[(2,4-dichloro-5-methoxyphenyl)amino]-7-methoxy-...)
Affinity DataIC50: 0.290nMpH: 7.5 T: 2°CAssay Description:Src kinase activity was measured in an ELISA format. IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the tra...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/15/2005
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 6470BDBM6470(4-[(4-chloro-5-methoxy-2-methylphenyl)amino]-7-met...)
Affinity DataIC50: 0.310nMpH: 7.5 T: 2°CAssay Description:Src kinase activity was measured in an ELISA format. IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the tra...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/15/2005
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 6474BDBM6474(4-[(2-chloro-5-methoxy-4-methylphenyl)amino]-7-met...)
Affinity DataIC50: 0.330nMpH: 7.5 T: 2°CAssay Description:Src kinase activity was measured in an ELISA format. IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the tra...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/15/2005
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 6471BDBM6471(4-[(2,4-dichloro-5-methoxyphenyl)amino]-7-methoxy-...)
Affinity DataIC50: 0.460nMpH: 7.5 T: 2°CAssay Description:Src kinase activity was measured in an ELISA format. IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the tra...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/15/2005
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 6476BDBM6476(4-[(2-chloro-4-fluoro-5-methoxyphenyl)amino]-7-met...)
Affinity DataIC50: 0.480nMpH: 7.5 T: 2°CAssay Description:Src kinase activity was measured in an ELISA format. IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the tra...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/15/2005
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 6475BDBM6475(4-[(2-chloro-5-methoxy-4-methylphenyl)amino]-8-[2-...)
Affinity DataIC50: 0.550nMpH: 7.5 T: 2°CAssay Description:Src kinase activity was measured in an ELISA format. IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the tra...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/15/2005
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 6473BDBM6473(4-[(2,4-dichloro-5-methoxyphenyl)amino]-8-[2-(4-hy...)
Affinity DataIC50: 0.720nMpH: 7.5 T: 2°CAssay Description:Src kinase activity was measured in an ELISA format. IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the tra...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/15/2005
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 6463BDBM6463(4-[(2,4-dichloro-5-methoxyphenyl)amino]-8-methoxy-...)
Affinity DataIC50: 1.10nMpH: 7.5 T: 2°CAssay Description:Src kinase activity was measured in an ELISA format. IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the tra...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/15/2005
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 6467BDBM6467(8-methoxy-7-[2-(morpholin-4-yl)ethoxy]-4-[(3,4,5-t...)
Affinity DataIC50: 1.20nMpH: 7.5 T: 2°CAssay Description:Src kinase activity was measured in an ELISA format. IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the tra...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/15/2005
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 4552BDBM4552(CHEMBL288441 | SKI-606 | 4-[(2,4-Dichloro-5-methox...)
Affinity DataIC50: 1.20nMpH: 7.5 T: 2°CAssay Description:Src kinase activity was measured in an ELISA format. IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the tra...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/15/2005
Entry Details Article
PubMedPDB3D3D Structure (crystal)
LigandChemical structure of BindingDB Monomer ID 6477BDBM6477(CHEMBL335025 | 4-[(4-chloro-5-methoxy-2-methylphen...)
Affinity DataIC50: 1.40nMpH: 7.5 T: 2°CAssay Description:Src kinase activity was measured in an ELISA format. IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the tra...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/15/2005
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 6461BDBM6461(4-[(4-chloro-5-methoxy-2-methylphenyl)amino]-8-met...)
Affinity DataIC50: 1.5nMpH: 7.5 T: 2°CAssay Description:Src kinase activity was measured in an ELISA format. IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the tra...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/15/2005
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 6462BDBM6462(4-[(2,4-dichloro-5-methoxyphenyl)amino]-8-methoxy-...)
Affinity DataIC50: 1.80nMpH: 7.5 T: 2°CAssay Description:Src kinase activity was measured in an ELISA format. IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the tra...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/15/2005
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 6464BDBM6464(4-[(2,4-dichloro-5-methoxyphenyl)amino]-7-[2-(4-hy...)
Affinity DataIC50: 2.10nMpH: 7.5 T: 2°CAssay Description:Src kinase activity was measured in an ELISA format. IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the tra...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/15/2005
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 6460BDBM6460(4-[(4-chloro-5-methoxy-2-methylphenyl)amino]-8-met...)
Affinity DataIC50: 2.10nMpH: 7.5 T: 2°CAssay Description:Src kinase activity was measured in an ELISA format. IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the tra...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/15/2005
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 6465BDBM6465(4-[(2-chloro-5-methoxy-4-methylphenyl)amino]-8-met...)
Affinity DataIC50: 2.5nMpH: 7.5 T: 2°CAssay Description:Src kinase activity was measured in an ELISA format. IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the tra...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/15/2005
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 6466BDBM6466(8-methoxy-7-[2-(4-methylpiperazin-1-yl)ethoxy]-4-[...)
Affinity DataIC50: 2.60nMpH: 7.5 T: 2°CAssay Description:Src kinase activity was measured in an ELISA format. IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the tra...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/15/2005
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 6468BDBM6468(4-[(2,4-dichlorophenyl)amino]-8-methoxy-7-[2-(morp...)
Affinity DataIC50: 13nMpH: 7.5 T: 2°CAssay Description:Src kinase activity was measured in an ELISA format. IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the tra...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/15/2005
Entry Details Article
PubMed