Compile Data Set for Download or QSAR
Report error Found 11 Enz. Inhib. hit(s) with all data for entry = 50004577
TargetFocal adhesion kinase 1(Human)
Nanjing University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 2579BDBM2579(CHEMBL388978 | Staurosporine, 8 | Staurosporin, 4 ...)
Affinity DataEC50:  2.35E+4nMAssay Description:Inhibition of human recombinant full-length FAK assessed as remaining ATP after 4 hrs by Kinase-Glo-luminescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/29/2020
Entry Details Article
PubMed
TargetFocal adhesion kinase 1(Human)
Nanjing University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50484318BDBM50484318(CHEMBL1834747)
Affinity DataEC50:  3.01E+4nMAssay Description:Inhibition of human recombinant full-length FAK assessed as remaining ATP after 4 hrs by Kinase-Glo-luminescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/29/2020
Entry Details Article
PubMed
TargetFocal adhesion kinase 1(Human)
Nanjing University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50484313BDBM50484313(CHEMBL1834737)
Affinity DataEC50:  3.09E+4nMAssay Description:Inhibition of human recombinant full-length FAK assessed as remaining ATP after 4 hrs by Kinase-Glo-luminescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/29/2020
Entry Details Article
PubMed
TargetFocal adhesion kinase 1(Human)
Nanjing University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50484315BDBM50484315(CHEMBL1834746)
Affinity DataEC50:  3.73E+4nMAssay Description:Inhibition of human recombinant full-length FAK assessed as remaining ATP after 4 hrs by Kinase-Glo-luminescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/29/2020
Entry Details Article
PubMed
TargetFocal adhesion kinase 1(Human)
Nanjing University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50484316BDBM50484316(CHEMBL1834741)
Affinity DataEC50:  3.81E+4nMAssay Description:Inhibition of human recombinant full-length FAK assessed as remaining ATP after 4 hrs by Kinase-Glo-luminescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/29/2020
Entry Details Article
PubMed
TargetFocal adhesion kinase 1(Human)
Nanjing University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50484314BDBM50484314(CHEMBL1834693)
Affinity DataEC50:  4.64E+4nMAssay Description:Inhibition of human recombinant full-length FAK assessed as remaining ATP after 4 hrs by Kinase-Glo-luminescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/29/2020
Entry Details Article
PubMed
TargetFocal adhesion kinase 1(Human)
Nanjing University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50484321BDBM50484321(CHEMBL1834689)
Affinity DataEC50:  5.09E+4nMAssay Description:Inhibition of human recombinant full-length FAK assessed as remaining ATP after 4 hrs by Kinase-Glo-luminescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/29/2020
Entry Details Article
PubMed
TargetFocal adhesion kinase 1(Human)
Nanjing University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50484322BDBM50484322(CHEMBL1834743)
Affinity DataEC50:  5.11E+4nMAssay Description:Inhibition of human recombinant full-length FAK assessed as remaining ATP after 4 hrs by Kinase-Glo-luminescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/29/2020
Entry Details Article
PubMed
TargetFocal adhesion kinase 1(Human)
Nanjing University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50484320BDBM50484320(CHEMBL1834739)
Affinity DataEC50:  5.55E+4nMAssay Description:Inhibition of human recombinant full-length FAK assessed as remaining ATP after 4 hrs by Kinase-Glo-luminescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/29/2020
Entry Details Article
PubMed
TargetFocal adhesion kinase 1(Human)
Nanjing University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50484319BDBM50484319(CHEMBL1834738)
Affinity DataEC50:  6.01E+4nMAssay Description:Inhibition of human recombinant full-length FAK assessed as remaining ATP after 4 hrs by Kinase-Glo-luminescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/29/2020
Entry Details Article
PubMed
TargetFocal adhesion kinase 1(Human)
Nanjing University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50484317BDBM50484317(CHEMBL1834690)
Affinity DataEC50:  6.18E+4nMAssay Description:Inhibition of human recombinant full-length FAK assessed as remaining ATP after 4 hrs by Kinase-Glo-luminescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/29/2020
Entry Details Article
PubMed