Compile Data Set for Download or QSAR
Report error Found 77 Enz. Inhib. hit(s) with all data for entry = 50005358
TargetProto-oncogene tyrosine-protein kinase Src(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50036013BDBM50036013(1,3N,3N-trimethyl-2-(3-dimethylcarbamoyl-1-methyl-...)
Affinity DataIC50: 500nMAssay Description:Inhibitory concentration of the against pp60v-src tyrosine kinase obtained from v-src baculovirus-infected insect cellsMore 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 Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 3351BDBM3351(CHEMBL336174 | 2-amino-3-[2-({3-[2-amino-2-(benzyl...)
Affinity DataIC50: 600nMAssay Description:Inhibitory concentration of the against pp60v-src tyrosine kinase obtained from v-src baculovirus-infected insect cellsMore 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 Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50036020BDBM50036020(2-(3-carbamoyl-1-methyl-1H-2-indolyldisulfanyl)-1-...)
Affinity DataIC50: 800nMAssay Description:Inhibitory concentration of the against pp60v-src tyrosine kinase obtained from v-src baculovirus-infected insect cellsMore 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 Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50036001BDBM50036001(4-{2-[3-(4-carboxybenzylcarbamoyl)-1-methyl-1H-2-i...)
Affinity DataIC50: 800nMAssay Description:Inhibitory concentration of the against pp60v-src tyrosine kinase obtained from v-src baculovirus-infected insect cellsMore 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 Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50035999BDBM50035999(({2-[3-(Carboxymethyl-carbamoyl)-1-methyl-1H-indol...)
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibitory concentration of the against pp60v-src tyrosine kinase obtained from v-src baculovirus-infected insect cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50036014BDBM50036014(3N-benzyl-2-(3-benzylcarbamoyl-1-methyl-1H-2-indol...)
Affinity DataIC50: 1.70E+3nMAssay Description:Inhibitory concentration compound against EFGR tyrosine kinase obtained from plasma membrane vesicles from cultured A431 cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 3350BDBM3350(N,1-dimethyl-2-{[1-methyl-3-(methylcarbamoyl)-1H-i...)
Affinity DataIC50: 1.80E+3nMAssay Description:Inhibitory concentration compound against EFGR tyrosine kinase obtained from plasma membrane vesicles from cultured A431 cellsMore 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 Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50035995BDBM50035995(methyl 4-{1-methyl-2-[1-methyl-3-(4-methyloxycarbo...)
Affinity DataIC50: 2.50E+3nMAssay Description:Inhibitory concentration of the against pp60v-src tyrosine kinase obtained from v-src baculovirus-infected insect cellsMore 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 Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50036015BDBM50036015([2-(3-Benzoyl-1-methyl-1H-indol-2-yldisulfanyl)-1-...)
Affinity DataIC50: 2.60E+3nMAssay Description:Inhibitory concentration of the against pp60v-src tyrosine kinase obtained from v-src baculovirus-infected insect cellsMore 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 Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 4016BDBM4016(1-methyl-2-{[1-methyl-3-(phenylcarbamoyl)-1H-indol...)
Affinity DataIC50: 3.20E+3nMAssay Description:Inhibitory concentration of the against pp60v-src tyrosine kinase obtained from v-src baculovirus-infected insect cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 3351BDBM3351(CHEMBL336174 | 2-amino-3-[2-({3-[2-amino-2-(benzyl...)
Affinity DataIC50: 3.30E+3nMAssay Description:Inhibitory concentration compound against EFGR tyrosine kinase obtained from plasma membrane vesicles from cultured A431 cellsMore 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 Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50036024BDBM50036024(2-{2-[3-(2-carboxyphenylcarbamoyl)-1-methyl-1H-2-i...)
Affinity DataIC50: 3.50E+3nMAssay Description:Inhibitory concentration of the against pp60v-src tyrosine kinase obtained from v-src baculovirus-infected insect cellsMore 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 Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50035993BDBM50035993(4-{2-[3-(4-carboxybenzoyl)-1-methyl-1H-2-indolyldi...)
Affinity DataIC50: 4.00E+3nMAssay Description:Inhibitory concentration of the against pp60v-src tyrosine kinase obtained from v-src baculovirus-infected insect cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 3979BDBM3979(2,2 -Dithiobis(1H-indole-3-propanoic acid) | 3-(2-...)
Affinity DataIC50: 4.20E+3nMAssay Description:Inhibitory concentration compound against EFGR tyrosine kinase obtained from plasma membrane vesicles from cultured A431 cellsMore 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 Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50036010BDBM50036010(methyl 4-{1-methyl-2-[1-methyl-3-(4-methyloxycarbo...)
Affinity DataIC50: 4.20E+3nMAssay Description:Inhibitory concentration of the against pp60v-src tyrosine kinase obtained from v-src baculovirus-infected insect cellsMore 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 Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50036016BDBM50036016(4-{2-[3-(4-carboxyphenylcarbamoyl)-1-methyl-1H-2-i...)
Affinity DataIC50: 4.30E+3nMAssay Description:Inhibitory concentration of the against pp60v-src tyrosine kinase obtained from v-src baculovirus-infected insect cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 4022BDBM4022(5-chloro-2-{[5-chloro-1-methyl-3-(phenylcarbamoyl)...)
Affinity DataIC50: 4.30E+3nMAssay Description:Inhibitory concentration compound against EFGR tyrosine kinase obtained from plasma membrane vesicles from cultured A431 cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50036020BDBM50036020(2-(3-carbamoyl-1-methyl-1H-2-indolyldisulfanyl)-1-...)
Affinity DataIC50: 4.70E+3nMAssay Description:Inhibitory concentration compound against EFGR tyrosine kinase obtained from plasma membrane vesicles from cultured A431 cellsMore 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 Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 3979BDBM3979(2,2 -Dithiobis(1H-indole-3-propanoic acid) | 3-(2-...)
Affinity DataIC50: 5.10E+3nMAssay Description:Inhibitory concentration of the against pp60v-src tyrosine kinase obtained from v-src baculovirus-infected insect cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50036001BDBM50036001(4-{2-[3-(4-carboxybenzylcarbamoyl)-1-methyl-1H-2-i...)
Affinity DataIC50: 5.30E+3nMAssay Description:Inhibitory concentration compound against EFGR tyrosine kinase obtained from plasma membrane vesicles from cultured A431 cellsMore 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 Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50035996BDBM50035996(3-{2-[3-(3-carboxyphenylcarbamoyl)-1-methyl-1H-2-i...)
Affinity DataIC50: 5.30E+3nMAssay Description:Inhibitory concentration of the against pp60v-src tyrosine kinase obtained from v-src baculovirus-infected insect cellsMore 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 Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50036017BDBM50036017(methyl 3-{1-methyl-2-[1-methyl-3-(3-methyloxycarbo...)
Affinity DataIC50: 5.40E+3nMAssay Description:Inhibitory concentration of the against pp60v-src tyrosine kinase obtained from v-src baculovirus-infected insect cellsMore 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 Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50036009BDBM50036009(di[3-(4-methylphenylsulfonyl)-1H-2-indolyl] disulf...)
Affinity DataIC50: 5.50E+3nMAssay Description:Inhibitory concentration of the against pp60v-src tyrosine kinase obtained from v-src baculovirus-infected insect cellsMore 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 Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50036006BDBM50036006(1,3N-dimethyl-3N-phenyl-2-[1-methyl-3-methyl(pheny...)
Affinity DataIC50: 5.50E+3nMAssay Description:Inhibitory concentration of the against pp60v-src tyrosine kinase obtained from v-src baculovirus-infected insect cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50035993BDBM50035993(4-{2-[3-(4-carboxybenzoyl)-1-methyl-1H-2-indolyldi...)
Affinity DataIC50: 5.50E+3nMAssay Description:Inhibitory concentration compound against EFGR tyrosine kinase obtained from plasma membrane vesicles from cultured A431 cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50036012BDBM50036012(1-[2-(3-Acetyl-1-methyl-1H-indol-2-yldisulfanyl)-1...)
Affinity DataIC50: 5.60E+3nMAssay Description:Inhibitory concentration compound against EFGR tyrosine kinase obtained from plasma membrane vesicles from cultured A431 cellsMore 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 Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 4028BDBM4028(1-methyl-2-{[1-methyl-3-(phenylcarbamoyl)-5-(trifl...)
Affinity DataIC50: 5.80E+3nMAssay Description:Inhibitory concentration of the against pp60v-src tyrosine kinase obtained from v-src baculovirus-infected insect cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50036011BDBM50036011(methyl 4-{1-methyl-2-[1-methyl-3-(4-methyloxycarbo...)
Affinity DataIC50: 6.10E+3nMAssay Description:Inhibitory concentration compound against EFGR tyrosine kinase obtained from plasma membrane vesicles from cultured A431 cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50036004BDBM50036004(3N-methyl-2-(3-methylcarbamoyl-1H-2-indolyldisulfa...)
Affinity DataIC50: 6.10E+3nMAssay Description:Inhibitory concentration compound against EFGR tyrosine kinase obtained from plasma membrane vesicles from cultured A431 cellsMore 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 Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 3350BDBM3350(N,1-dimethyl-2-{[1-methyl-3-(methylcarbamoyl)-1H-i...)
Affinity DataIC50: 6.70E+3nMAssay Description:Inhibitory concentration of the against pp60v-src tyrosine kinase obtained from v-src baculovirus-infected insect cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50036019BDBM50036019(2-(3-cyano-1-methyl-1H-2-indolyldisulfanyl)-1-meth...)
Affinity DataIC50: 6.90E+3nMAssay Description:Inhibitory concentration compound against EFGR tyrosine kinase obtained from plasma membrane vesicles from cultured A431 cellsMore 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 Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50036011BDBM50036011(methyl 4-{1-methyl-2-[1-methyl-3-(4-methyloxycarbo...)
Affinity DataIC50: 7.10E+3nMAssay Description:Inhibitory concentration of the against pp60v-src tyrosine kinase obtained from v-src baculovirus-infected insect cellsMore 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 Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50035998BDBM50035998(3N-phenyl-2-(3-phenylcarbamoyl-1H-2-indolyldisulfa...)
Affinity DataIC50: 7.60E+3nMAssay Description:Inhibitory concentration of the against pp60v-src tyrosine kinase obtained from v-src baculovirus-infected insect cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50036023BDBM50036023({2-[3-(Furan-2-carbonyl)-1-methyl-1H-indol-2-yldis...)
Affinity DataIC50: 7.70E+3nMAssay Description:Inhibitory concentration compound against EFGR tyrosine kinase obtained from plasma membrane vesicles from cultured A431 cellsMore 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 Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50036004BDBM50036004(3N-methyl-2-(3-methylcarbamoyl-1H-2-indolyldisulfa...)
Affinity DataIC50: 7.90E+3nMAssay Description:Inhibitory concentration of the against pp60v-src tyrosine kinase obtained from v-src baculovirus-infected insect cellsMore 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 Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50036014BDBM50036014(3N-benzyl-2-(3-benzylcarbamoyl-1-methyl-1H-2-indol...)
Affinity DataIC50: 8.00E+3nMAssay Description:Inhibitory concentration of the against pp60v-src tyrosine kinase obtained from v-src baculovirus-infected insect cellsMore 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 Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50036023BDBM50036023({2-[3-(Furan-2-carbonyl)-1-methyl-1H-indol-2-yldis...)
Affinity DataIC50: 8.30E+3nMAssay Description:Inhibitory concentration of the against pp60v-src tyrosine kinase obtained from v-src baculovirus-infected insect cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50035999BDBM50035999(({2-[3-(Carboxymethyl-carbamoyl)-1-methyl-1H-indol...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibitory concentration compound against EFGR tyrosine kinase obtained from plasma membrane vesicles from cultured A431 cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 4016BDBM4016(1-methyl-2-{[1-methyl-3-(phenylcarbamoyl)-1H-indol...)
Affinity DataIC50: 1.09E+4nMAssay Description:Inhibitory concentration compound against EFGR tyrosine kinase obtained from plasma membrane vesicles from cultured A431 cellsMore 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 Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50036012BDBM50036012(1-[2-(3-Acetyl-1-methyl-1H-indol-2-yldisulfanyl)-1...)
Affinity DataIC50: 1.15E+4nMAssay Description:Inhibitory concentration of the against pp60v-src tyrosine kinase obtained from v-src baculovirus-infected insect cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50035996BDBM50035996(3-{2-[3-(3-carboxyphenylcarbamoyl)-1-methyl-1H-2-i...)
Affinity DataIC50: 1.20E+4nMAssay Description:Inhibitory concentration compound against EFGR tyrosine kinase obtained from plasma membrane vesicles from cultured A431 cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50035995BDBM50035995(methyl 4-{1-methyl-2-[1-methyl-3-(4-methyloxycarbo...)
Affinity DataIC50: 1.30E+4nMAssay Description:Inhibitory concentration compound against EFGR tyrosine kinase obtained from plasma membrane vesicles from cultured A431 cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50036008BDBM50036008(3N-benzyl-2-(3-benzylcarbamoyl-1H-2-indolyldisulfa...)
Affinity DataIC50: 1.50E+4nMAssay Description:Inhibitory concentration compound against EFGR tyrosine kinase obtained from plasma membrane vesicles from cultured A431 cellsMore 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 Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50036000BDBM50036000(3N-(2-dimethylaminoethyl)-2-[3-(2-dimethylaminoeth...)
Affinity DataIC50: 1.52E+4nMAssay Description:Inhibitory concentration of the against pp60v-src tyrosine kinase obtained from v-src baculovirus-infected insect cellsMore 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 Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50036022BDBM50036022(methyl 2-{1-methyl-2-[1-methyl-3-(2-methyloxycarbo...)
Affinity DataIC50: 1.56E+4nMAssay Description:Inhibitory concentration of the against pp60v-src tyrosine kinase obtained from v-src baculovirus-infected insect cellsMore 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 Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50036008BDBM50036008(3N-benzyl-2-(3-benzylcarbamoyl-1H-2-indolyldisulfa...)
Affinity DataIC50: 1.63E+4nMAssay Description:Inhibitory concentration of the against pp60v-src tyrosine kinase obtained from v-src baculovirus-infected insect cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50036016BDBM50036016(4-{2-[3-(4-carboxyphenylcarbamoyl)-1-methyl-1H-2-i...)
Affinity DataIC50: 1.69E+4nMAssay Description:Inhibitory concentration compound against EFGR tyrosine kinase obtained from plasma membrane vesicles from cultured A431 cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50036000BDBM50036000(3N-(2-dimethylaminoethyl)-2-[3-(2-dimethylaminoeth...)
Affinity DataIC50: 1.75E+4nMAssay Description:Inhibitory concentration compound against EFGR tyrosine kinase obtained from plasma membrane vesicles from cultured A431 cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50036013BDBM50036013(1,3N,3N-trimethyl-2-(3-dimethylcarbamoyl-1-methyl-...)
Affinity DataIC50: 2.12E+4nMAssay Description:Inhibitory concentration compound against EFGR tyrosine kinase obtained from plasma membrane vesicles from cultured A431 cellsMore 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 Auckland

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50036003BDBM50036003(3N-(2,3-dihydroxypropyl)-2-[3-(2,3-dihydroxypropyl...)
Affinity DataIC50: 2.25E+4nMAssay Description:Inhibitory concentration of the against pp60v-src tyrosine kinase obtained from v-src baculovirus-infected insect cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
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