Compile Data Set for Download or QSAR
Report error Found 14 Enz. Inhib. hit(s) with all data for entry = 50023104
TargetALK tyrosine kinase receptor(Human)
Sungkyunkwan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50362781BDBM50362781(CHEMBL1738797 | US9126931, 366 | Alectinib | 12565...)
Affinity DataIC50: 2.80nMAssay Description:Inhibition of wild type ALK (unknown origin) by Eurofins kinase profiler methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/5/2026
Entry Details
PubMed
TargetALK tyrosine kinase receptor(Human)
Sungkyunkwan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50436850BDBM50436850(CHEMBL2403108 | CERITINIB | US10053458, Comparativ...)
Affinity DataIC50: 2.90nMAssay Description:Inhibition of wild type ALK (unknown origin) by Eurofins kinase profiler methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/5/2026
Entry Details
PubMedPDB3D3D Structure (crystal)
TargetALK tyrosine kinase receptor(Human)
Sungkyunkwan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50185140BDBM50185140(AP-26113 | Brigatinib | US11248003, Example Brigat...)
Affinity DataIC50: 3.5nMAssay Description:Inhibition of wild type ALK (unknown origin) by Eurofins kinase profiler methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/5/2026
Entry Details
PubMedPDB3D3D Structure (crystal)
TargetALK tyrosine kinase receptor(Human)
Sungkyunkwan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50659171BDBM50659171(CHEMBL6151640)
Affinity DataIC50: 5.40nMAssay Description:Inhibition of wild type ALK (unknown origin) by Eurofins kinase profiler methodMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/5/2026
Entry Details
PubMed
TargetALK tyrosine kinase receptor(Human)
Sungkyunkwan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50659166BDBM50659166(CHEMBL6151097)
Affinity DataIC50: 13nMAssay Description:Inhibition of wild type ALK (unknown origin) by Eurofins kinase profiler methodMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/5/2026
Entry Details
PubMed
TargetALK tyrosine kinase receptor(Human)
Sungkyunkwan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50306682BDBM50306682((R)-3-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)-5-(1...)
Affinity DataIC50: 20nMAssay Description:Inhibition of wild type ALK (unknown origin) by Eurofins kinase profiler methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/5/2026
Entry Details
PubMed
TargetALK tyrosine kinase receptor(Human)
Sungkyunkwan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50659173BDBM50659173(CHEMBL6148710)
Affinity DataIC50: 24nMAssay Description:Inhibition of wild type ALK (unknown origin) by Eurofins kinase profiler methodMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/5/2026
Entry Details
PubMed
TargetALK tyrosine kinase receptor(Human)
Sungkyunkwan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50659172BDBM50659172(CHEMBL6161691)
Affinity DataIC50: 25nMAssay Description:Inhibition of wild type ALK (unknown origin) by Eurofins kinase profiler methodMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/5/2026
Entry Details
PubMed
TargetALK tyrosine kinase receptor(Human)
Sungkyunkwan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50659167BDBM50659167(CHEMBL6170640)
Affinity DataIC50: 70nMAssay Description:Inhibition of wild type ALK (unknown origin) by Eurofins kinase profiler methodMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/5/2026
Entry Details
PubMed
TargetEpidermal growth factor receptor(Human)
Sungkyunkwan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50659166BDBM50659166(CHEMBL6151097)
Affinity DataIC50: 97nMAssay Description:Inhibition of EGFR L858R (unknown origin) by Eurofins kinase profiler methodMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/5/2026
Entry Details
PubMed
TargetProto-oncogene tyrosine-protein kinase ROS(Human)
Sungkyunkwan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50659166BDBM50659166(CHEMBL6151097)
Affinity DataIC50: 185nMAssay Description:Inhibition of ROS (unknown origin) by Eurofins kinase profiler methodMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/5/2026
Entry Details
PubMed
TargetALK tyrosine kinase receptor(Human)
Sungkyunkwan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50659169BDBM50659169(CHEMBL6170625)
Affinity DataIC50: 206nMAssay Description:Inhibition of wild type ALK (unknown origin) by Eurofins kinase profiler methodMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/5/2026
Entry Details
PubMed
TargetALK tyrosine kinase receptor(Human)
Sungkyunkwan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50659168BDBM50659168(CHEMBL6143473)
Affinity DataIC50: 225nMAssay Description:Inhibition of wild type ALK (unknown origin) by Eurofins kinase profiler methodMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/5/2026
Entry Details
PubMed
TargetALK tyrosine kinase receptor(Human)
Sungkyunkwan University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50659170BDBM50659170(CHEMBL6142577)
Affinity DataIC50: 630nMAssay Description:Inhibition of wild type ALK (unknown origin) by Eurofins kinase profiler methodMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/5/2026
Entry Details
PubMed