Compile Data Set for Download or QSAR
Report error Found 46 Enz. Inhib. hit(s) with all data for entry = 521
TargetEpidermal growth factor receptor(Human)
University of Auckland

LigandChemical structure of BindingDB Monomer ID 3309BDBM3309(4-N-(3-bromophenyl)pyrido[4,3-d]pyrimidine-4,7-dia...)
Affinity DataIC50: 10nMpH: 7.4 T: 2°CAssay Description:IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2005
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

LigandChemical structure of BindingDB Monomer ID 3312BDBM3312(7-amino-4-[[3-(trifluoromethyl)phenyl]amino]pyrido...)
Affinity DataIC50: 15nMpH: 7.4 T: 2°CAssay Description:IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2005
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

LigandChemical structure of BindingDB Monomer ID 3327BDBM3327(4-N-(3-methylphenyl)pyrido[4,3-d]pyrimidine-4,7-di...)
Affinity DataIC50: 40nMAssay Description:IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2005
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

LigandChemical structure of BindingDB Monomer ID 3306BDBM3306(4-N-(3-nitrophenyl)pyrido[4,3-d]pyrimidine-4,7-dia...)
Affinity DataIC50: 40nMpH: 7.4 T: 2°CAssay Description:IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2005
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

LigandChemical structure of BindingDB Monomer ID 3326BDBM3326(3-({7-aminopyrido[4,3-d]pyrimidin-4-yl}amino)pheno...)
Affinity DataIC50: 70nMAssay Description:IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2005
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

LigandChemical structure of BindingDB Monomer ID 3310BDBM3310(7-amino-4-[(4-bromophenyl)amino]pyrido[4,3-d]pyrim...)
Affinity DataIC50: 90nMpH: 7.4 T: 2°CAssay Description:IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2005
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

LigandChemical structure of BindingDB Monomer ID 3324BDBM3324(7-amino-4[(3-chlorophenyl)amino]pyrido[4,3-d]pyrim...)
Affinity DataIC50: 120nMAssay Description:IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2005
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

LigandChemical structure of BindingDB Monomer ID 3315BDBM3315(4-N-(3-methoxyphenyl)pyrido[4,3-d]pyrimidine-4,7-d...)
Affinity DataIC50: 130nMpH: 7.4 T: 2°CAssay Description:IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2005
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

LigandChemical structure of BindingDB Monomer ID 3344BDBM3344(4-N-[(2-aminophenyl)methyl]pyrido[4,3-d]pyrimidine...)
Affinity DataIC50: 230nMAssay Description:IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2005
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

LigandChemical structure of BindingDB Monomer ID 3308BDBM3308(7-amino-4-[(2-bromophenyl)amino]pyrido[4,3-d]pyrim...)
Affinity DataIC50: 240nMpH: 7.4 T: 2°CAssay Description:IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2005
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

LigandChemical structure of BindingDB Monomer ID 3304BDBM3304(7-amino-4-(phenylamino)pyrido[4,3-d]pyrimidine | 4...)
Affinity DataIC50: 250nMpH: 7.4 T: 2°CAssay Description:IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2005
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

LigandChemical structure of BindingDB Monomer ID 3325BDBM3325(4-N-(3-iodophenyl)pyrido[4,3-d]pyrimidine-4,7-diam...)
Affinity DataIC50: 260nMAssay Description:IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2005
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

LigandChemical structure of BindingDB Monomer ID 3331BDBM3331(4-N-benzylpyrido[4,3-d]pyrimidine-4,7-diamine | CH...)
Affinity DataIC50: 580nMAssay Description:IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2005
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

LigandChemical structure of BindingDB Monomer ID 3316BDBM3316(4-N-(4-methoxyphenyl)pyrido[4,3-d]pyrimidine-4,7-d...)
Affinity DataIC50: 670nMpH: 7.4 T: 2°CAssay Description:IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2005
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

LigandChemical structure of BindingDB Monomer ID 3323BDBM3323(4-N-(3-fluorophenyl)pyrido[4,3-d]pyrimidine-4,7-di...)
Affinity DataIC50: 840nMAssay Description:IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2005
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

LigandChemical structure of BindingDB Monomer ID 3336BDBM3336(4-N-[(3-bromophenyl)methyl]pyrido[4,3-d]pyrimidine...)
Affinity DataIC50: 1.00E+3nMAssay Description:IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2005
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

LigandChemical structure of BindingDB Monomer ID 3305BDBM3305(7-amino-4-[(2-nitrophenyl)amino]pyrido[4,3-d]pyrim...)
Affinity DataIC50: 1.25E+3nMpH: 7.4 T: 2°CAssay Description:IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2005
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

LigandChemical structure of BindingDB Monomer ID 3318BDBM3318(4-N-(3-aminophenyl)pyrido[4,3-d]pyrimidine-4,7-dia...)
Affinity DataIC50: 1.55E+3nMpH: 7.4 T: 2°CAssay Description:IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2005
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

LigandChemical structure of BindingDB Monomer ID 3335BDBM3335(4-N-[(2-bromophenyl)methyl]pyrido[4,3-d]pyrimidine...)
Affinity DataIC50: 1.67E+3nMAssay Description:IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2005
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

LigandChemical structure of BindingDB Monomer ID 3321BDBM3321(4-N-[3-(dimethylamino)phenyl]pyrido[4,3-d]pyrimidi...)
Affinity DataIC50: 1.79E+3nMAssay Description:IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2005
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

LigandChemical structure of BindingDB Monomer ID 3339BDBM3339(4-N-{[3-(trifluoromethyl)phenyl]methyl}pyrido[4,3-...)
Affinity DataIC50: 1.95E+3nMAssay Description:IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2005
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

LigandChemical structure of BindingDB Monomer ID 3337BDBM3337(4-N-[(4-bromophenyl)methyl]pyrido[4,3-d]pyrimidine...)
Affinity DataIC50: 2.46E+3nMAssay Description:IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2005
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

LigandChemical structure of BindingDB Monomer ID 3342BDBM3342(4-N-[(3-methoxyphenyl)methyl]pyrido[4,3-d]pyrimidi...)
Affinity DataIC50: 2.87E+3nMAssay Description:IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2005
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

LigandChemical structure of BindingDB Monomer ID 3314BDBM3314(4-N-(2-methoxyphenyl)pyrido[4,3-d]pyrimidine-4,7-d...)
Affinity DataIC50: 3.71E+3nMpH: 7.4 T: 2°CAssay Description:IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2005
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

LigandChemical structure of BindingDB Monomer ID 3332BDBM3332(7-amino-4-[[(2-nitrophenyl)methyl]amino]pyrido[4,3...)
Affinity DataIC50: 4.25E+3nMAssay Description:IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2005
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

LigandChemical structure of BindingDB Monomer ID 3313BDBM3313(4-N-[4-(trifluoromethyl)phenyl]pyrido[4,3-d]pyrimi...)
Affinity DataIC50: 4.70E+3nMpH: 7.4 T: 2°CAssay Description:IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2005
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

LigandChemical structure of BindingDB Monomer ID 3322BDBM3322(7-amino-4-[[4-(dimethylamino)phenyl]amino]pyrido[4...)
Affinity DataIC50: 4.86E+3nMAssay Description:IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2005
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

LigandChemical structure of BindingDB Monomer ID 3317BDBM3317(4-N-(2-aminophenyl)pyrido[4,3-d]pyrimidine-4,7-dia...)
Affinity DataIC50: 5.25E+3nMpH: 7.4 T: 2°CAssay Description:IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2005
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

LigandChemical structure of BindingDB Monomer ID 3319BDBM3319(4-N-(4-aminophenyl)pyrido[4,3-d]pyrimidine-4,7-dia...)
Affinity DataIC50: 5.90E+3nMpH: 7.4 T: 2°CAssay Description:IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2005
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

LigandChemical structure of BindingDB Monomer ID 3340BDBM3340(7-amino-4-[[[4-(trifluoromethyl)phenyllmethyl]amin...)
Affinity DataIC50: 8.00E+3nMAssay Description:IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2005
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

LigandChemical structure of BindingDB Monomer ID 3311BDBM3311(7-Amino-4-[2-(trifluoromethyl)phenyl]amino]pyrido[...)
Affinity DataIC50: 1.00E+4nMpH: 7.4 T: 2°CAssay Description:IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2005
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

LigandChemical structure of BindingDB Monomer ID 3328BDBM3328(7-amino-4-[(3-pyridyl)amino]pyrido[4,3-d]pyrimidin...)
Affinity DataIC50: 1.00E+4nMAssay Description:IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2005
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

LigandChemical structure of BindingDB Monomer ID 3345BDBM3345(7-amino-4-[[(3-aminophenyl)methyl]amino]pyrido[4,3...)
Affinity DataIC50: 1.00E+4nMAssay Description:IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2005
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

LigandChemical structure of BindingDB Monomer ID 3329BDBM3329(N-[3-({7-aminopyrido[4,3-d]pyrimidin-4-yl}amino)ph...)
Affinity DataIC50: 1.00E+4nMAssay Description:IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2005
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

LigandChemical structure of BindingDB Monomer ID 3346BDBM3346(4-N-[(4-aminophenyl)methyl]pyrido[4,3-d]pyrimidine...)
Affinity DataIC50: 1.00E+4nMAssay Description:IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2005
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

LigandChemical structure of BindingDB Monomer ID 3330BDBM3330(7-amino-4-[(4-acetamidophenyl)amino]pyrido[4,3-d]p...)
Affinity DataIC50: 1.00E+4nMAssay Description:IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2005
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

LigandChemical structure of BindingDB Monomer ID 3348BDBM3348(4-N-{[3-(dimethylamino)phenyl]methyl}pyrido[4,3-d]...)
Affinity DataIC50: 1.00E+4nMAssay Description:IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2005
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

LigandChemical structure of BindingDB Monomer ID 3334BDBM3334(7-amino-4-[[(4-nitrophenyl)methyl]amino]pyrido[4,3...)
Affinity DataIC50: 1.00E+4nMAssay Description:IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2005
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

LigandChemical structure of BindingDB Monomer ID 3338BDBM3338(4-N-{[2-(trifluoromethyl)phenyl]methyl}pyrido[4,3-...)
Affinity DataIC50: 1.00E+4nMAssay Description:IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2005
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

LigandChemical structure of BindingDB Monomer ID 3333BDBM3333(4-N-[(3-nitrophenyl)methyl]pyrido[4,3-d]pyrimidine...)
Affinity DataIC50: 1.01E+4nMAssay Description:IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2005
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

LigandChemical structure of BindingDB Monomer ID 3307BDBM3307(4-N-(4-nitrophenyl)pyrido[4,3-d]pyrimidine-4,7-dia...)
Affinity DataIC50: 6.50E+4nMpH: 7.4 T: 2°CAssay Description:IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2005
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

LigandChemical structure of BindingDB Monomer ID 3320BDBM3320(4-N-[2-(dimethylamino)phenyl]pyrido[4,3-d]pyrimidi...)
Affinity DataIC50: 6.90E+4nMAssay Description:IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2005
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

LigandChemical structure of BindingDB Monomer ID 3341BDBM3341(4-N-[(2-methoxyphenyl)methyl]pyrido[4,3-d]pyrimidi...)
Affinity DataIC50: 1.00E+5nMAssay Description:IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2005
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

LigandChemical structure of BindingDB Monomer ID 3343BDBM3343(4-N-[(4-methoxyphenyl)methyl]pyrido[4,3-d]pyrimidi...)
Affinity DataIC50: 1.00E+5nMAssay Description:IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2005
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

LigandChemical structure of BindingDB Monomer ID 3347BDBM3347(4-N-{[2-(dimethylamino)phenyl]methyl}pyrido[4,3-d]...)
Affinity DataIC50: 1.00E+5nMAssay Description:IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2005
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

LigandChemical structure of BindingDB Monomer ID 3349BDBM3349(4-N-{[4-(dimethylamino)phenyl]methyl}pyrido[4,3-d]...)
Affinity DataIC50: 1.00E+5nMAssay Description:IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/21/2005
Entry Details Article
PubMed