Compile Data Set for Download or QSAR
Report error Found 16 Enz. Inhib. hit(s) with all data for entry = 50023815
TargetFocal adhesion kinase 1(Human)
Beijing Normal University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50668598BDBM50668598(CHEMBL6189535)
Affinity DataIC50: 0.870nMAssay Description:Inhibition of FAK (unknown origin) by HTRF assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetFocal adhesion kinase 1(Human)
Beijing Normal University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 418817BDBM418817(US10450297, Example 317 | US10450297, Example 318 ...)
Affinity DataIC50: 1.5nMAssay Description:Inhibition of FAK (unknown origin) by HTRF assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetFocal adhesion kinase 1(Human)
Beijing Normal University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50668599BDBM50668599(CHEMBL6192379)
Affinity DataIC50: 3.40nMAssay Description:Inhibition of FAK (unknown origin) by HTRF assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetFocal adhesion kinase 1(Human)
Beijing Normal University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50668600BDBM50668600(CHEMBL6192544)
Affinity DataIC50: 3.5nMAssay Description:Inhibition of FAK (unknown origin) by HTRF assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetFocal adhesion kinase 1(Human)
Beijing Normal University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50668603BDBM50668603(CHEMBL6188680)
Affinity DataIC50: 6.80nMAssay Description:Inhibition of FAK (unknown origin) by HTRF assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetFocal adhesion kinase 1(Human)
Beijing Normal University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50668605BDBM50668605(CHEMBL6188917)
Affinity DataIC50: 9.90nMAssay Description:Inhibition of FAK (unknown origin) by HTRF assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetFocal adhesion kinase 1(Human)
Beijing Normal University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50668606BDBM50668606(CHEMBL6188768)
Affinity DataIC50: 11nMAssay Description:Inhibition of FAK (unknown origin) by HTRF assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetFocal adhesion kinase 1(Human)
Beijing Normal University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50668601BDBM50668601(CHEMBL6190099)
Affinity DataIC50: 26nMAssay Description:Inhibition of FAK (unknown origin) by HTRF assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetFocal adhesion kinase 1(Human)
Beijing Normal University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50668609BDBM50668609(CHEMBL6188878)
Affinity DataIC50: 33nMAssay Description:Inhibition of FAK (unknown origin) by HTRF assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetFocal adhesion kinase 1(Human)
Beijing Normal University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50668608BDBM50668608(CHEMBL6189653)
Affinity DataIC50: 47nMAssay Description:Inhibition of FAK (unknown origin) by HTRF assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetFocal adhesion kinase 1(Human)
Beijing Normal University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50668610BDBM50668610(CHEMBL6189849)
Affinity DataIC50: 47nMAssay Description:Inhibition of FAK (unknown origin) by HTRF assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetFocal adhesion kinase 1(Human)
Beijing Normal University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50668604BDBM50668604(CHEMBL6191041)
Affinity DataIC50: 56nMAssay Description:Inhibition of FAK (unknown origin) by HTRF assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetFocal adhesion kinase 1(Human)
Beijing Normal University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50668602BDBM50668602(CHEMBL6188852)
Affinity DataIC50: 65nMAssay Description:Inhibition of FAK (unknown origin) by HTRF assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetFocal adhesion kinase 1(Human)
Beijing Normal University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50668607BDBM50668607(CHEMBL6190740)
Affinity DataIC50: 66nMAssay Description:Inhibition of FAK (unknown origin) by HTRF assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetFocal adhesion kinase 1(Human)
Beijing Normal University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50668598BDBM50668598(CHEMBL6189535)
Affinity DataKd:  1.50E+4nMAssay Description:Binding affinity to FAK (unknown origin) assessed as dissociation constant by SPR analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetFocal adhesion kinase 1(Human)
Beijing Normal University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 418817BDBM418817(US10450297, Example 317 | US10450297, Example 318 ...)
Affinity DataKd:  1.60E+4nMAssay Description:Binding affinity to FAK (unknown origin) assessed as dissociation constant by SPR analysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed