Compile Data Set for Download or QSAR
Report error Found 88 Enz. Inhib. hit(s) with all data for entry = 50018189
TargetEpidermal growth factor receptor(Human)
Imclone Systems

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50192487BDBM50192487((7,8-dimethoxy-10,11-dihydro-5H-2,4,5,11-tetraaza-...)
Affinity DataIC50: 150nMAssay Description:Inhibition of EGFR measured as pGAT-biotin peptide phosphorylation in presence of 2.0 uM ATP by HTRF assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Imclone Systems

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50192474BDBM50192474(benzyl-(7,8-dimethoxy-10,11-dihydro-5H-2,4,5,11-te...)
Affinity DataIC50: 200nMAssay Description:Inhibition of EGFR measured as pGAT-biotin peptide phosphorylation in presence of 2.0 uM ATP by HTRF assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Imclone Systems

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50192477BDBM50192477((3-chloro-2-fluoro-phenyl)-(7,8-dimethoxy-10,11-di...)
Affinity DataIC50: 300nMAssay Description:Inhibition of EGFR measured as pGAT-biotin peptide phosphorylation in presence of 2.0 uM ATP by HTRF assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Imclone Systems

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50180448BDBM50180448((3-Bromo-phenyl)-(7,8-dimethoxy-10,11-dihydro-5-ox...)
Affinity DataIC50: 300nMAssay Description:Inhibition of EGFR measured as pGAT-biotin peptide phosphorylation in presence of 2.0 uM ATP by HTRF assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Imclone Systems

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50192498BDBM50192498((3-chloro-4-fluoro-benzyl)-(7,8-dimethoxy-10,11-di...)
Affinity DataIC50: 300nMAssay Description:Inhibition of EGFR measured as pGAT-biotin peptide phosphorylation in presence of 2.0 uM ATP by HTRF assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Imclone Systems

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50180448BDBM50180448((3-Bromo-phenyl)-(7,8-dimethoxy-10,11-dihydro-5-ox...)
Affinity DataIC50: 500nMAssay Description:Inhibition of EGFR autophosphorylation in DiFi cells by ELISAMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Imclone Systems

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50192487BDBM50192487((7,8-dimethoxy-10,11-dihydro-5H-2,4,5,11-tetraaza-...)
Affinity DataIC50: 500nMAssay Description:Inhibition of EGFR autophosphorylation in DiFi cells by ELISAMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Imclone Systems

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50192471BDBM50192471((7,8-dimethoxy-10,11-dihydro-5-oxa-2,4,11-triaza-d...)
Affinity DataIC50: 500nMAssay Description:Inhibition of EGFR measured as pGAT-biotin peptide phosphorylation in presence of 2.0 uM ATP by HTRF assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Imclone Systems

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50192478BDBM50192478(1-(3-bromo-phenoxy)-7,8-dimethoxy-10,11-dihydro-5-...)
Affinity DataIC50: 700nMAssay Description:Inhibition of EGFR measured as pGAT-biotin peptide phosphorylation in presence of 2.0 uM ATP by HTRF assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Imclone Systems

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50180453BDBM50180453((3-Chloro-4-fluoro-phenyl)-(7,8-dimethoxy-10,11-di...)
Affinity DataIC50: 700nMAssay Description:Inhibition of EGFR autophosphorylation in DiFi cells by ELISAMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Imclone Systems

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50192497BDBM50192497((7,8-dimethoxy-10,11-dihydro-5H-2,4,5,11-tetraaza-...)
Affinity DataIC50: 800nMAssay Description:Inhibition of EGFR measured as pGAT-biotin peptide phosphorylation in presence of 2.0 uM ATP by HTRF assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Imclone Systems

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50192501BDBM50192501((7,8-dimethoxy-10,11-dihydro-5-oxa-2,4,11-triaza-d...)
Affinity DataIC50: 900nMAssay Description:Inhibition of EGFR autophosphorylation in DiFi cells by ELISAMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Imclone Systems

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50192474BDBM50192474(benzyl-(7,8-dimethoxy-10,11-dihydro-5H-2,4,5,11-te...)
Affinity DataIC50: 900nMAssay Description:Inhibition of EGFR autophosphorylation in DiFi cells by ELISAMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Imclone Systems

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50192496BDBM50192496(1-(3-chloro-phenylsulfanyl)-7,8-dimethoxy-10,11-di...)
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of EGFR measured as pGAT-biotin peptide phosphorylation in presence of 2.0 uM ATP by HTRF assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Imclone Systems

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50192479BDBM50192479((5-chloro-2-fluoro-phenyl)-(7,8-dimethoxy-10,11-di...)
Affinity DataIC50: 1.10E+3nMAssay Description:Inhibition of EGFR measured as pGAT-biotin peptide phosphorylation in presence of 2.0 uM ATP by HTRF assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Imclone Systems

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50192480BDBM50192480((7,8-dimethoxy-10,11-dihydro-5-oxa-2,4,11-triaza-d...)
Affinity DataIC50: 1.20E+3nMAssay Description:Inhibition of EGFR measured as pGAT-biotin peptide phosphorylation in presence of 2.0 uM ATP by HTRF assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Imclone Systems

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50192489BDBM50192489(1-(3-bromo-phenylsulfanyl)-7,8-dimethoxy-10,11-dih...)
Affinity DataIC50: 1.20E+3nMAssay Description:Inhibition of EGFR autophosphorylation in DiFi cells by ELISAMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Imclone Systems

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50180453BDBM50180453((3-Chloro-4-fluoro-phenyl)-(7,8-dimethoxy-10,11-di...)
Affinity DataIC50: 1.20E+3nMAssay Description:Inhibition of EGFR measured as pGAT-biotin peptide phosphorylation in presence of 2.0 uM ATP by HTRF assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Imclone Systems

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50192473BDBM50192473(7-(3-bromophenoxy)-13,14-dimethoxy-9-methyl-2-oxa-...)
Affinity DataIC50: 1.20E+3nMAssay Description:Inhibition of EGFR measured as pGAT-biotin peptide phosphorylation in presence of 2.0 uM ATP by HTRF assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Imclone Systems

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50192489BDBM50192489(1-(3-bromo-phenylsulfanyl)-7,8-dimethoxy-10,11-dih...)
Affinity DataIC50: 1.30E+3nMAssay Description:Inhibition of EGFR measured as pGAT-biotin peptide phosphorylation in presence of 2.0 uM ATP by HTRF assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Imclone Systems

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50192500BDBM50192500((3-bromo-phenyl)-(7,8-dimethoxy-10,11-dihydro-5H-2...)
Affinity DataIC50: 1.50E+3nMAssay Description:Inhibition of EGFR measured as pGAT-biotin peptide phosphorylation in presence of 2.0 uM ATP by HTRF assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Imclone Systems

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50192483BDBM50192483(1-(3-bromo-phenylsulfanyl)-7,8-dimethoxy-10,11-dih...)
Affinity DataIC50: 1.60E+3nMAssay Description:Inhibition of EGFR measured as pGAT-biotin peptide phosphorylation in presence of 2.0 uM ATP by HTRF assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Imclone Systems

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50192498BDBM50192498((3-chloro-4-fluoro-benzyl)-(7,8-dimethoxy-10,11-di...)
Affinity DataIC50: 1.60E+3nMAssay Description:Inhibition of EGFR autophosphorylation in DiFi cells by ELISAMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Imclone Systems

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50192478BDBM50192478(1-(3-bromo-phenoxy)-7,8-dimethoxy-10,11-dihydro-5-...)
Affinity DataIC50: 1.80E+3nMAssay Description:Inhibition of EGFR autophosphorylation in DiFi cells by ELISAMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetVascular endothelial growth factor receptor 2(Human)
Imclone Systems

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50192474BDBM50192474(benzyl-(7,8-dimethoxy-10,11-dihydro-5H-2,4,5,11-te...)
Affinity DataIC50: 2.00E+3nMAssay Description:Inhibition of KDR measured as pGAT-biotin peptide phosphorylation by HTRF assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetVascular endothelial growth factor receptor 2(Human)
Imclone Systems

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50192498BDBM50192498((3-chloro-4-fluoro-benzyl)-(7,8-dimethoxy-10,11-di...)
Affinity DataIC50: 2.00E+3nMAssay Description:Inhibition of KDR measured as pGAT-biotin peptide phosphorylation by HTRF assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetVascular endothelial growth factor receptor 2(Human)
Imclone Systems

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50192497BDBM50192497((7,8-dimethoxy-10,11-dihydro-5H-2,4,5,11-tetraaza-...)
Affinity DataIC50: 2.00E+3nMAssay Description:Inhibition of KDR measured as pGAT-biotin peptide phosphorylation by HTRF assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetVascular endothelial growth factor receptor 2(Human)
Imclone Systems

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50192487BDBM50192487((7,8-dimethoxy-10,11-dihydro-5H-2,4,5,11-tetraaza-...)
Affinity DataIC50: 2.00E+3nMAssay Description:Inhibition of KDR measured as pGAT-biotin peptide phosphorylation by HTRF assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Imclone Systems

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50192471BDBM50192471((7,8-dimethoxy-10,11-dihydro-5-oxa-2,4,11-triaza-d...)
Affinity DataIC50: 2.30E+3nMAssay Description:Inhibition of EGFR autophosphorylation in DiFi cells by ELISAMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Imclone Systems

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50192496BDBM50192496(1-(3-chloro-phenylsulfanyl)-7,8-dimethoxy-10,11-di...)
Affinity DataIC50: 2.40E+3nMAssay Description:Inhibition of EGFR autophosphorylation in DiFi cells by ELISAMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Imclone Systems

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50192475BDBM50192475(1-(3-chloro-phenylsulfanyl)-7,8-dimethoxy-10,11-di...)
Affinity DataIC50: 2.90E+3nMAssay Description:Inhibition of EGFR measured as pGAT-biotin peptide phosphorylation in presence of 2.0 uM ATP by HTRF assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Imclone Systems

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50192501BDBM50192501((7,8-dimethoxy-10,11-dihydro-5-oxa-2,4,11-triaza-d...)
Affinity DataIC50: 3.20E+3nMAssay Description:Inhibition of EGFR measured as pGAT-biotin peptide phosphorylation in presence of 2.0 uM ATP by HTRF assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Imclone Systems

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50192493BDBM50192493((2-chloro-4-fluoro-phenyl)-(7,8-dimethoxy-10,11-di...)
Affinity DataIC50: 3.40E+3nMAssay Description:Inhibition of EGFR measured as pGAT-biotin peptide phosphorylation in presence of 2.0 uM ATP by HTRF assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Imclone Systems

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50192479BDBM50192479((5-chloro-2-fluoro-phenyl)-(7,8-dimethoxy-10,11-di...)
Affinity DataIC50: 3.90E+3nMAssay Description:Inhibition of EGFR autophosphorylation in DiFi cells by ELISAMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Imclone Systems

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50192472BDBM50192472((7,8-dimethoxy-10,11-dihydro-5-oxa-2,4,11-triaza-d...)
Affinity DataIC50: 4.40E+3nMAssay Description:Inhibition of EGFR autophosphorylation in DiFi cells by ELISAMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Imclone Systems

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50192477BDBM50192477((3-chloro-2-fluoro-phenyl)-(7,8-dimethoxy-10,11-di...)
Affinity DataIC50: 4.60E+3nMAssay Description:Inhibition of EGFR autophosphorylation in DiFi cells by ELISAMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Imclone Systems

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50192486BDBM50192486(1-(3-chloro-2-fluoro-phenoxy)-7,8-dimethoxy-10,11-...)
Affinity DataIC50: 4.60E+3nMAssay Description:Inhibition of EGFR measured as pGAT-biotin peptide phosphorylation in presence of 2.0 uM ATP by HTRF assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Imclone Systems

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50192491BDBM50192491(benzothiazol-6-yl-(7,8-dimethoxy-10,11-dihydro-5-o...)
Affinity DataIC50: 5.60E+3nMAssay Description:Inhibition of EGFR measured as pGAT-biotin peptide phosphorylation in presence of 2.0 uM ATP by HTRF assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Imclone Systems

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50192509BDBM50192509((3-bromo-phenyl)-(7,8-dimethoxy-10,11-dihydro-5-th...)
Affinity DataIC50: 5.90E+3nMAssay Description:Inhibition of EGFR measured as pGAT-biotin peptide phosphorylation in presence of 2.0 uM ATP by HTRF assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Imclone Systems

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50192473BDBM50192473(7-(3-bromophenoxy)-13,14-dimethoxy-9-methyl-2-oxa-...)
Affinity DataIC50: 6.10E+3nMAssay Description:Inhibition of EGFR autophosphorylation in DiFi cells by ELISAMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Imclone Systems

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50192490BDBM50192490((7,8-dimethoxy-10,11-dihydro-5-oxa-2,4,11-triaza-d...)
Affinity DataIC50: 7.10E+3nMAssay Description:Inhibition of EGFR measured as pGAT-biotin peptide phosphorylation in presence of 2.0 uM ATP by HTRF assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Imclone Systems

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50192472BDBM50192472((7,8-dimethoxy-10,11-dihydro-5-oxa-2,4,11-triaza-d...)
Affinity DataIC50: 7.40E+3nMAssay Description:Inhibition of EGFR measured as pGAT-biotin peptide phosphorylation in presence of 2.0 uM ATP by HTRF assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Imclone Systems

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50192490BDBM50192490((7,8-dimethoxy-10,11-dihydro-5-oxa-2,4,11-triaza-d...)
Affinity DataIC50: 7.60E+3nMAssay Description:Inhibition of EGFR autophosphorylation in DiFi cells by ELISAMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Imclone Systems

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50192512BDBM50192512((3-chloro-4-fluoro-phenyl)-(7,8-dimethoxy-10,11-di...)
Affinity DataIC50: 8.20E+3nMAssay Description:Inhibition of EGFR measured as pGAT-biotin peptide phosphorylation in presence of 2.0 uM ATP by HTRF assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Imclone Systems

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50192484BDBM50192484((4-bromo-phenyl)-(7,8-dimethoxy-10,11-dihydro-5-ox...)
Affinity DataIC50: 8.70E+3nMAssay Description:Inhibition of EGFR measured as pGAT-biotin peptide phosphorylation in presence of 2.0 uM ATP by HTRF assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetVascular endothelial growth factor receptor 2(Human)
Imclone Systems

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50192473BDBM50192473(7-(3-bromophenoxy)-13,14-dimethoxy-9-methyl-2-oxa-...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of KDR measured as pGAT-biotin peptide phosphorylation by HTRF assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetVascular endothelial growth factor receptor 2(Human)
Imclone Systems

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50180448BDBM50180448((3-Bromo-phenyl)-(7,8-dimethoxy-10,11-dihydro-5-ox...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of KDR measured as pGAT-biotin peptide phosphorylation by HTRF assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetVascular endothelial growth factor receptor 2(Human)
Imclone Systems

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50192501BDBM50192501((7,8-dimethoxy-10,11-dihydro-5-oxa-2,4,11-triaza-d...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of KDR measured as pGAT-biotin peptide phosphorylation by HTRF assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetVascular endothelial growth factor receptor 2(Human)
Imclone Systems

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50192476BDBM50192476((3-bromo-phenyl)-(7,8-dimethoxy-3-methyl-10,11-dih...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of KDR measured as pGAT-biotin peptide phosphorylation by HTRF assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetVascular endothelial growth factor receptor 2(Human)
Imclone Systems

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50192477BDBM50192477((3-chloro-2-fluoro-phenyl)-(7,8-dimethoxy-10,11-di...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of KDR measured as pGAT-biotin peptide phosphorylation by HTRF assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
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