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Found 20 Enz. Inhib. hit(s) with all data for entry = 50015914
TargetFocal adhesion kinase 1(Homo sapiens (Human))
Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50590475(CHEMBL5170906)
Affinity DataIC50:  0.100nMAssay Description:Inhibition of recombinant human FAK (393 to 698 residues) using poly (4:1 Glu, Tyr) peptide as substrate incubated for 60 mins in presence of ATP by ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
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TargetFocal adhesion kinase 1(Homo sapiens (Human))
Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50590490(CHEMBL5198068)
Affinity DataIC50:  0.108nMAssay Description:Inhibition of recombinant human FAK (393 to 698 residues) using poly (4:1 Glu, Tyr) peptide as substrate incubated for 60 mins in presence of ATP by ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
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TargetFocal adhesion kinase 1(Homo sapiens (Human))
Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50590479(CHEMBL5196177)
Affinity DataIC50:  0.117nMAssay Description:Inhibition of recombinant human FAK (393 to 698 residues) using poly (4:1 Glu, Tyr) peptide as substrate incubated for 60 mins in presence of ATP by ...More data for this Ligand-Target Pair
In DepthDetails PubMed
TargetFocal adhesion kinase 1(Homo sapiens (Human))
Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50590489(CHEMBL5176233)
Affinity DataIC50:  0.124nMAssay Description:Inhibition of recombinant human FAK (393 to 698 residues) using poly (4:1 Glu, Tyr) peptide as substrate incubated for 60 mins in presence of ATP by ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
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TargetFocal adhesion kinase 1(Homo sapiens (Human))
Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50590488(CHEMBL5206909)
Affinity DataIC50:  0.153nMAssay Description:Inhibition of recombinant human FAK (393 to 698 residues) using poly (4:1 Glu, Tyr) peptide as substrate incubated for 60 mins in presence of ATP by ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
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TargetFocal adhesion kinase 1(Homo sapiens (Human))
Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50590483(CHEMBL5187385)
Affinity DataIC50:  0.161nMAssay Description:Inhibition of recombinant human FAK (393 to 698 residues) using poly (4:1 Glu, Tyr) peptide as substrate incubated for 60 mins in presence of ATP by ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
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TargetFocal adhesion kinase 1(Homo sapiens (Human))
Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50590484(CHEMBL5190968)
Affinity DataIC50:  0.192nMAssay Description:Inhibition of recombinant human FAK (393 to 698 residues) using poly (4:1 Glu, Tyr) peptide as substrate incubated for 60 mins in presence of ATP by ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetFocal adhesion kinase 1(Homo sapiens (Human))
Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50590485(CHEMBL5177776)
Affinity DataIC50:  0.194nMAssay Description:Inhibition of recombinant human FAK (393 to 698 residues) using poly (4:1 Glu, Tyr) peptide as substrate incubated for 60 mins in presence of ATP by ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetFocal adhesion kinase 1(Homo sapiens (Human))
Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50590474(CHEMBL5176990)
Affinity DataIC50:  0.213nMAssay Description:Inhibition of recombinant human FAK (393 to 698 residues) using poly (4:1 Glu, Tyr) peptide as substrate incubated for 60 mins in presence of ATP by ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetFocal adhesion kinase 1(Homo sapiens (Human))
Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50590477(CHEMBL5204729)
Affinity DataIC50:  0.275nMAssay Description:Inhibition of recombinant human FAK (393 to 698 residues) using poly (4:1 Glu, Tyr) peptide as substrate incubated for 60 mins in presence of ATP by ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetFocal adhesion kinase 1(Homo sapiens (Human))
Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50590482(CHEMBL5186801)
Affinity DataIC50:  0.296nMAssay Description:Inhibition of recombinant human FAK (393 to 698 residues) using poly (4:1 Glu, Tyr) peptide as substrate incubated for 60 mins in presence of ATP by ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetFocal adhesion kinase 1(Homo sapiens (Human))
Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50590487(CHEMBL5199835)
Affinity DataIC50:  0.315nMAssay Description:Inhibition of recombinant human FAK (393 to 698 residues) using poly (4:1 Glu, Tyr) peptide as substrate incubated for 60 mins in presence of ATP by ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetFocal adhesion kinase 1(Homo sapiens (Human))
Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50590476(CHEMBL5178369)
Affinity DataIC50:  0.315nMAssay Description:Inhibition of recombinant human FAK (393 to 698 residues) using poly (4:1 Glu, Tyr) peptide as substrate incubated for 60 mins in presence of ATP by ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetFocal adhesion kinase 1(Homo sapiens (Human))
Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50590486(CHEMBL5177168)
Affinity DataIC50:  0.514nMAssay Description:Inhibition of recombinant human FAK (393 to 698 residues) using poly (4:1 Glu, Tyr) peptide as substrate incubated for 60 mins in presence of ATP by ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetFocal adhesion kinase 1(Homo sapiens (Human))
Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50590473(CHEMBL5192604)
Affinity DataIC50:  0.579nMAssay Description:Inhibition of recombinant human FAK (393 to 698 residues) using poly (4:1 Glu, Tyr) peptide as substrate incubated for 60 mins in presence of ATP by ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetFocal adhesion kinase 1(Homo sapiens (Human))
Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50590481(CHEMBL5180558)
Affinity DataIC50:  0.976nMAssay Description:Inhibition of recombinant human FAK (393 to 698 residues) using poly (4:1 Glu, Tyr) peptide as substrate incubated for 60 mins in presence of ATP by ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetFocal adhesion kinase 1(Homo sapiens (Human))
Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50590480(CHEMBL5195974)
Affinity DataIC50:  1.30nMAssay Description:Inhibition of recombinant human FAK (393 to 698 residues) using poly (4:1 Glu, Tyr) peptide as substrate incubated for 60 mins in presence of ATP by ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetFocal adhesion kinase 1(Homo sapiens (Human))
Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50590478(CHEMBL5197230)
Affinity DataIC50:  1.40nMAssay Description:Inhibition of recombinant human FAK (393 to 698 residues) using poly (4:1 Glu, Tyr) peptide as substrate incubated for 60 mins in presence of ATP by ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
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TargetFocal adhesion kinase 1(Homo sapiens (Human))
Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50334594(2-(5-chloro-2-(2-methoxy-4-morpholinophenylamino)p...)
Affinity DataIC50:  4.5nMAssay Description:Inhibition of recombinant human FAK (393 to 698 residues) using poly (4:1 Glu, Tyr) peptide as substrate incubated for 60 mins in presence of ATP by ...More data for this Ligand-Target Pair
TargetFocal adhesion kinase 1(Homo sapiens (Human))
Dalian Medical University

Curated by ChEMBL
LigandPNGBDBM50590472(CHEMBL5188293)
Affinity DataIC50:  7.60nMAssay Description:Inhibition of recombinant human FAK (393 to 698 residues) using poly (4:1 Glu, Tyr) peptide as substrate incubated for 60 mins in presence of ATP by ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed