Compile Data Set for Download or QSAR

Found 23 hits of Enzyme Inhibition Constant Data   

TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50286755(8-Methoxy-5,10-dihydro-3H-pyrimido[4,5-b]quinolin-...)copy SMILEScopy InChI
Affinity DataIC50: 500nMAssay Description:Inhibition of cellular oncogene pp60 c-srcMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DJ5FKR
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50132155(7,8-Dimethoxy-5,10-dihydro-1H-pyrimido[4,5-b]quino...)copy SMILEScopy InChI
Affinity DataIC50: 500nMAssay Description:Inhibition of cellular oncogene pp60 c-srcMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DJ5FKR
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50286752(7,8-Dimethoxy-3-methyl-5,10-dihydro-3H-pyrimido[4,...)copy SMILEScopy InChI
Affinity DataIC50: 1.20E+3nMAssay Description:Inhibition of cellular oncogene pp60 c-srcMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DJ5FKR
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50286758(7-Methoxy-5,10-dihydro-3H-pyrimido[4,5-b]quinolin-...)copy SMILEScopy InChI
Affinity DataIC50: 3.70E+3nMAssay Description:Inhibition of cellular oncogene pp60 c-srcMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DJ5FKR
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50286753(5,10-Dihydro-3H-pyrimido[4,5-b]quinolin-4-one | CH...)copy SMILEScopy InChI
Affinity DataIC50: 9.10E+3nMAssay Description:Inhibition of cellular oncogene pp60 c-srcMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DJ5FKR
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50132157(7,8-Dimethoxy-1H-pyrimido[4,5-b]quinolin-4-one | 7...)copy SMILEScopy InChI
Affinity DataIC50: 3.20E+4nMAssay Description:Inhibition of cellular oncogene pp60 c-srcMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DJ5FKR
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50286759(2-Ethyl-5,10-dihydro-3H-pyrimido[4,5-b]quinolin-4-...)copy SMILEScopy InChI
Affinity DataIC50: 3.80E+4nMAssay Description:Inhibition of cellular oncogene pp60 c-srcMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DJ5FKR
TargetEpidermal growth factor receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50132155(7,8-Dimethoxy-5,10-dihydro-1H-pyrimido[4,5-b]quino...)copy SMILEScopy InChI
Affinity DataIC50: 7.50E+4nMAssay Description:Inhibition of epidermal growth factor receptor (EGFR)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DJ5FKR
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50286757(7,8-Dimethoxy-3-(2-morpholin-4-yl-ethyl)-5,10-dihy...)copy SMILEScopy InChI
Affinity DataIC50: 1.05E+5nMAssay Description:Inhibition of cellular oncogene pp60 c-srcMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DJ5FKR
TargetEpidermal growth factor receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50286752(7,8-Dimethoxy-3-methyl-5,10-dihydro-3H-pyrimido[4,...)copy SMILEScopy InChI
Affinity DataIC50: 1.60E+5nMAssay Description:Inhibition of epidermal growth factor receptor (EGFR)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DJ5FKR
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50286751(3,9-Dihydro-pyrimido[4,5-b]indol-4-one | CHEMBL267...)copy SMILEScopy InChI
Affinity DataIC50: 2.93E+5nMAssay Description:Inhibition of cellular oncogene pp60 c-srcMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DJ5FKR
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50286754(10-Ethyl-5,10-dihydro-3H-pyrimido[4,5-b]quinolin-4...)copy SMILEScopy InChI
Affinity DataIC50: 5.50E+5nMAssay Description:Inhibition of cellular oncogene pp60 c-srcMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DJ5FKR
LigandPNGBDBM50132157(7,8-Dimethoxy-1H-pyrimido[4,5-b]quinolin-4-one | 7...)copy SMILEScopy InChI
Affinity DataIC50: 7.50E+5nMAssay Description:Inhibition of cAMP-dependent kinase (Protein kinase A)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DJ5FKR
LigandPNGBDBM50286754(10-Ethyl-5,10-dihydro-3H-pyrimido[4,5-b]quinolin-4...)copy SMILEScopy InChI
Affinity DataIC50: 9.60E+5nMAssay Description:Inhibition of cAMP-dependent kinase (Protein kinase A)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DJ5FKR
LigandPNGBDBM50286757(7,8-Dimethoxy-3-(2-morpholin-4-yl-ethyl)-5,10-dihy...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+6nMAssay Description:Inhibition of cAMP-dependent kinase (Protein kinase A)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DJ5FKR
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50286756(6-Phenylamino-3H-pyrimidin-4-one | CHEMBL7052)copy SMILEScopy InChI
Affinity DataIC50: 1.55E+6nMAssay Description:Inhibition of cellular oncogene pp60 c-srcMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DJ5FKR
LigandPNGBDBM50286753(5,10-Dihydro-3H-pyrimido[4,5-b]quinolin-4-one | CH...)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+6nMAssay Description:Inhibition of cAMP-dependent kinase (Protein kinase A)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DJ5FKR
LigandPNGBDBM50286759(2-Ethyl-5,10-dihydro-3H-pyrimido[4,5-b]quinolin-4-...)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+6nMAssay Description:Inhibition of cAMP-dependent kinase (Protein kinase A)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DJ5FKR
LigandPNGBDBM50286755(8-Methoxy-5,10-dihydro-3H-pyrimido[4,5-b]quinolin-...)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+6nMAssay Description:Inhibition of cAMP-dependent kinase (Protein kinase A)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DJ5FKR
LigandPNGBDBM50286758(7-Methoxy-5,10-dihydro-3H-pyrimido[4,5-b]quinolin-...)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+6nMAssay Description:Inhibition of cAMP-dependent kinase (Protein kinase A)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DJ5FKR
LigandPNGBDBM50286752(7,8-Dimethoxy-3-methyl-5,10-dihydro-3H-pyrimido[4,...)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+6nMAssay Description:Inhibition of cAMP-dependent kinase (Protein kinase A)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DJ5FKR
LigandPNGBDBM50132155(7,8-Dimethoxy-5,10-dihydro-1H-pyrimido[4,5-b]quino...)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+6nMAssay Description:Inhibition of cAMP-dependent kinase (Protein kinase A)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DJ5FKR
LigandPNGBDBM50286756(6-Phenylamino-3H-pyrimidin-4-one | CHEMBL7052)copy SMILEScopy InChI
Affinity DataIC50: 4.00E+6nMAssay Description:Inhibition of cAMP-dependent kinase (Protein kinase A)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DJ5FKR
* indicates data uncertainty>20%