Compile Data Set for Download or QSAR
Report error Found 42 Enz. Inhib. hit(s) with all data for entry = 50005236
TargetReceptor tyrosine-protein kinase erbB-2(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50489209BDBM50489209(Metachromin P)
Affinity DataIC50: 4.17E+4nMAssay Description:Inhibition of HER2 (unknown origin) by Z-LYTE assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/31/2020
Entry Details Article
PubMed
TargetReceptor tyrosine-protein kinase erbB-2(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50489219BDBM50489219(Metachromin Q)
Affinity DataIC50: 5.09E+4nMAssay Description:Inhibition of HER2 (unknown origin) by Z-LYTE assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/31/2020
Entry Details Article
PubMed
TargetReceptor tyrosine-protein kinase erbB-2(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50489210BDBM50489210(Metachromin O)
Affinity DataIC50: 6.05E+4nMAssay Description:Inhibition of HER2 (unknown origin) by Z-LYTE assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/31/2020
Entry Details Article
PubMed
TargetReceptor tyrosine-protein kinase erbB-2(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50489202BDBM50489202(Nakijiquinone C)
Affinity DataIC50: 6.95E+4nMAssay Description:Inhibition of HER2 (unknown origin) by Z-LYTE assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/31/2020
Entry Details Article
PubMed
TargetReceptor tyrosine-protein kinase erbB-2(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50489205BDBM50489205(CHEMBL2315697)
Affinity DataIC50: 7.89E+4nMAssay Description:Inhibition of HER2 (unknown origin) by Z-LYTE assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/31/2020
Entry Details Article
PubMed
TargetReceptor tyrosine-protein kinase erbB-2(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50489212BDBM50489212(CHEMBL2315699)
Affinity DataIC50: 8.34E+4nMAssay Description:Inhibition of HER2 (unknown origin) by Z-LYTE assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/31/2020
Entry Details Article
PubMed
TargetReceptor tyrosine-protein kinase erbB-2(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50489218BDBM50489218(CHEMBL2315408)
Affinity DataIC50: 8.97E+4nMAssay Description:Inhibition of HER2 (unknown origin) by Z-LYTE assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/31/2020
Entry Details Article
PubMed
TargetReceptor tyrosine-protein kinase erbB-2(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50489201BDBM50489201(CHEMBL2315696)
Affinity DataIC50: 1.03E+5nMAssay Description:Inhibition of HER2 (unknown origin) by Z-LYTE assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/31/2020
Entry Details Article
PubMed
TargetReceptor tyrosine-protein kinase erbB-2(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50489204BDBM50489204(CHEMBL2315698)
Affinity DataIC50: 1.42E+5nMAssay Description:Inhibition of HER2 (unknown origin) by Z-LYTE assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/31/2020
Entry Details Article
PubMed
TargetReceptor tyrosine-protein kinase erbB-2(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50489214BDBM50489214(CHEMBL2315409)
Affinity DataIC50: 1.79E+5nMAssay Description:Inhibition of HER2 (unknown origin) by Z-LYTE assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/31/2020
Entry Details Article
PubMed
TargetReceptor tyrosine-protein kinase erbB-2(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50489215BDBM50489215(Metachromin M)
Affinity DataIC50: 1.96E+5nMAssay Description:Inhibition of HER2 (unknown origin) by Z-LYTE assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/31/2020
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50489214BDBM50489214(CHEMBL2315409)
Affinity DataIC50: 2.10E+5nMAssay Description:Inhibition of EGFR (unknown origin) by Z-LYTE assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/31/2020
Entry Details Article
PubMed
TargetReceptor tyrosine-protein kinase erbB-2(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50489207BDBM50489207(CHEMBL2315406)
Affinity DataIC50: 2.15E+5nMAssay Description:Inhibition of HER2 (unknown origin) by Z-LYTE assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/31/2020
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50489213BDBM50489213(CHEMBL2315410)
Affinity DataIC50: 2.69E+5nMAssay Description:Inhibition of EGFR (unknown origin) by Z-LYTE assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/31/2020
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50489202BDBM50489202(Nakijiquinone C)
Affinity DataIC50: 2.89E+5nMAssay Description:Inhibition of EGFR (unknown origin) by Z-LYTE assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/31/2020
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50489204BDBM50489204(CHEMBL2315698)
Affinity DataIC50: 2.93E+5nMAssay Description:Inhibition of EGFR (unknown origin) by Z-LYTE assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/31/2020
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50489205BDBM50489205(CHEMBL2315697)
Affinity DataIC50: 2.93E+5nMAssay Description:Inhibition of EGFR (unknown origin) by Z-LYTE assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/31/2020
Entry Details Article
PubMed
TargetReceptor tyrosine-protein kinase erbB-2(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50489211BDBM50489211(Metachromin L)
Affinity DataIC50: 3.11E+5nMAssay Description:Inhibition of HER2 (unknown origin) by Z-LYTE assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/31/2020
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50489212BDBM50489212(CHEMBL2315699)
Affinity DataIC50: 3.33E+5nMAssay Description:Inhibition of EGFR (unknown origin) by Z-LYTE assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/31/2020
Entry Details Article
PubMed
TargetReceptor tyrosine-protein kinase erbB-2(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50489221BDBM50489221(Metachromin N)
Affinity DataIC50: 4.26E+5nMAssay Description:Inhibition of HER2 (unknown origin) by Z-LYTE assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/31/2020
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50489201BDBM50489201(CHEMBL2315696)
Affinity DataIC50: 4.35E+5nMAssay Description:Inhibition of EGFR (unknown origin) by Z-LYTE assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/31/2020
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50489218BDBM50489218(CHEMBL2315408)
Affinity DataIC50: 4.48E+5nMAssay Description:Inhibition of EGFR (unknown origin) by Z-LYTE assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/31/2020
Entry Details Article
PubMed
TargetReceptor tyrosine-protein kinase erbB-2(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50489213BDBM50489213(CHEMBL2315410)
Affinity DataIC50: 4.48E+5nMAssay Description:Inhibition of HER2 (unknown origin) by Z-LYTE assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/31/2020
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50489210BDBM50489210(Metachromin O)
Affinity DataIC50: 4.48E+5nMAssay Description:Inhibition of EGFR (unknown origin) by Z-LYTE assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/31/2020
Entry Details Article
PubMed
TargetReceptor tyrosine-protein kinase erbB-2(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50489208BDBM50489208(CHEMBL2315405)
Affinity DataIC50: 4.48E+5nMAssay Description:Inhibition of HER2 (unknown origin) by Z-LYTE assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/31/2020
Entry Details Article
PubMed
TargetReceptor tyrosine-protein kinase erbB-2(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50489220BDBM50489220(CHEMBL2315407)
Affinity DataIC50: 4.48E+5nMAssay Description:Inhibition of HER2 (unknown origin) by Z-LYTE assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/31/2020
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50489208BDBM50489208(CHEMBL2315405)
Affinity DataIC50: 4.48E+5nMAssay Description:Inhibition of EGFR (unknown origin) by Z-LYTE assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/31/2020
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50489221BDBM50489221(Metachromin N)
Affinity DataIC50: 4.48E+5nMAssay Description:Inhibition of EGFR (unknown origin) by Z-LYTE assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/31/2020
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50489207BDBM50489207(CHEMBL2315406)
Affinity DataIC50: 4.48E+5nMAssay Description:Inhibition of EGFR (unknown origin) by Z-LYTE assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/31/2020
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50489220BDBM50489220(CHEMBL2315407)
Affinity DataIC50: 4.48E+5nMAssay Description:Inhibition of EGFR (unknown origin) by Z-LYTE assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/31/2020
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50489217BDBM50489217(CHEMBL2315695)
Affinity DataIC50: 4.63E+5nMAssay Description:Inhibition of EGFR (unknown origin) by Z-LYTE assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/31/2020
Entry Details Article
PubMed
TargetReceptor tyrosine-protein kinase erbB-2(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50489206BDBM50489206(CHEMBL2315411)
Affinity DataIC50: 4.63E+5nMAssay Description:Inhibition of HER2 (unknown origin) by Z-LYTE assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/31/2020
Entry Details Article
PubMed
TargetReceptor tyrosine-protein kinase erbB-2(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50489217BDBM50489217(CHEMBL2315695)
Affinity DataIC50: 4.63E+5nMAssay Description:Inhibition of HER2 (unknown origin) by Z-LYTE assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/31/2020
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50489209BDBM50489209(Metachromin P)
Affinity DataIC50: 4.63E+5nMAssay Description:Inhibition of EGFR (unknown origin) by Z-LYTE assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/31/2020
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50489219BDBM50489219(Metachromin Q)
Affinity DataIC50: 4.63E+5nMAssay Description:Inhibition of EGFR (unknown origin) by Z-LYTE assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/31/2020
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50489206BDBM50489206(CHEMBL2315411)
Affinity DataIC50: 4.63E+5nMAssay Description:Inhibition of EGFR (unknown origin) by Z-LYTE assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/31/2020
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50489211BDBM50489211(Metachromin L)
Affinity DataIC50: 4.90E+5nMAssay Description:Inhibition of EGFR (unknown origin) by Z-LYTE assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/31/2020
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50489215BDBM50489215(Metachromin M)
Affinity DataIC50: 4.98E+5nMAssay Description:Inhibition of EGFR (unknown origin) by Z-LYTE assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/31/2020
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50489216BDBM50489216(Metachromin C)
Affinity DataIC50: 5.57E+5nMAssay Description:Inhibition of EGFR (unknown origin) by Z-LYTE assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/31/2020
Entry Details Article
PubMed
TargetReceptor tyrosine-protein kinase erbB-2(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50489203BDBM50489203(METACHROMIN A)
Affinity DataIC50: 5.57E+5nMAssay Description:Inhibition of HER2 (unknown origin) by Z-LYTE assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/31/2020
Entry Details Article
PubMed
TargetReceptor tyrosine-protein kinase erbB-2(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50489216BDBM50489216(Metachromin C)
Affinity DataIC50: 5.57E+5nMAssay Description:Inhibition of HER2 (unknown origin) by Z-LYTE assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/31/2020
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50489203BDBM50489203(METACHROMIN A)
Affinity DataIC50: 5.57E+5nMAssay Description:Inhibition of EGFR (unknown origin) by Z-LYTE assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/31/2020
Entry Details Article
PubMed