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Report error Found 30 Enz. Inhib. hit(s) with all data for entry = 50019459
TargetFocal adhesion kinase 1(Human)
Shenyang Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50568532(CHEMBL4742157)
Affinity DataIC50: 0.400nMAssay Description:Inhibition of FAK (unknown origin)More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetFocal adhesion kinase 1(Human)
Shenyang Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM418817(US10450297, Example 317 | US10450297, Example 318 ...)
Affinity DataIC50: 0.600nMAssay Description:Inhibition of FAK (unknown origin)More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetFocal adhesion kinase 1(Human)
Shenyang Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM134067(US8846689, 69)
Affinity DataIC50: 1nMAssay Description:Inhibition of FAK (unknown origin)More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetFocal adhesion kinase 1(Human)
Shenyang Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM379139(2-(2-(2-Methoxy-4-morpholinophenylamino)-5-(triflu...)
Affinity DataIC50: 1.5nMAssay Description:Inhibition of GST-fused FAK (411 to 686 residues)(unknown origin) expressed in baculovirus expression system using poly(Glu:Tyr) as substrate incubat...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetFocal adhesion kinase 1(Human)
Shenyang Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50334594(2-(5-chloro-2-(2-methoxy-4-morpholinophenylamino)p...)
Affinity DataIC50: 5.5nMAssay Description:Inhibition of FAK (unknown origin)More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMedPDB3D3D Structure (crystal)
TargetFocal adhesion kinase 1(Human)
Shenyang Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50334594(2-(5-chloro-2-(2-methoxy-4-morpholinophenylamino)p...)
Affinity DataIC50: 6.30nMAssay Description:Inhibition of FAK (unknown origin) incubated for 50 mins in presence of substrate/ATP by HTRF assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMedPDB3D3D Structure (crystal)
TargetFocal adhesion kinase 1(Human)
Shenyang Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50619421(CHEMBL5429220)
Affinity DataIC50: 6.70nMAssay Description:Inhibition of FAK (unknown origin) incubated for 50 mins in presence of substrate/ATP by HTRF assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetFocal adhesion kinase 1(Human)
Shenyang Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50619407(CHEMBL5406670)
Affinity DataIC50: 8.70nMAssay Description:Inhibition of FAK (unknown origin) incubated for 50 mins in presence of substrate/ATP by HTRF assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetFocal adhesion kinase 1(Human)
Shenyang Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50619412(CHEMBL5402799)
Affinity DataIC50: 9.60nMAssay Description:Inhibition of FAK (unknown origin) incubated for 50 mins in presence of substrate/ATP by HTRF assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetFocal adhesion kinase 1(Human)
Shenyang Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50619418(CHEMBL5420280)
Affinity DataIC50: 10nMAssay Description:Inhibition of FAK (unknown origin) incubated for 50 mins in presence of substrate/ATP by HTRF assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetFocal adhesion kinase 1(Human)
Shenyang Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50619411(CHEMBL5414280)
Affinity DataIC50: 11nMAssay Description:Inhibition of FAK (unknown origin) incubated for 50 mins in presence of substrate/ATP by HTRF assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetFocal adhesion kinase 1(Human)
Shenyang Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50619408(CHEMBL5434288)
Affinity DataIC50: 14nMAssay Description:Inhibition of FAK (unknown origin) incubated for 50 mins in presence of substrate/ATP by HTRF assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetFocal adhesion kinase 1(Human)
Shenyang Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50619415(CHEMBL5433832)
Affinity DataIC50: 15nMAssay Description:Inhibition of FAK (unknown origin) incubated for 50 mins in presence of substrate/ATP by HTRF assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetFocal adhesion kinase 1(Human)
Shenyang Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50619420(CHEMBL5433341)
Affinity DataIC50: 16nMAssay Description:Inhibition of FAK (unknown origin) incubated for 50 mins in presence of substrate/ATP by HTRF assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetFocal adhesion kinase 1(Human)
Shenyang Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50619416(CHEMBL5394494)
Affinity DataIC50: 16nMAssay Description:Inhibition of FAK (unknown origin) incubated for 50 mins in presence of substrate/ATP by HTRF assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetFocal adhesion kinase 1(Human)
Shenyang Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50619409(CHEMBL5414496)
Affinity DataIC50: 17nMAssay Description:Inhibition of FAK (unknown origin) incubated for 50 mins in presence of substrate/ATP by HTRF assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetFocal adhesion kinase 1(Human)
Shenyang Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50619414(CHEMBL5415868)
Affinity DataIC50: 18nMAssay Description:Inhibition of FAK (unknown origin) incubated for 50 mins in presence of substrate/ATP by HTRF assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetFocal adhesion kinase 1(Human)
Shenyang Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50619410(CHEMBL5427011)
Affinity DataIC50: 20nMAssay Description:Inhibition of FAK (unknown origin) incubated for 50 mins in presence of substrate/ATP by HTRF assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetFocal adhesion kinase 1(Human)
Shenyang Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50619419(CHEMBL5431569)
Affinity DataIC50: 28nMAssay Description:Inhibition of FAK (unknown origin) incubated for 50 mins in presence of substrate/ATP by HTRF assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetFocal adhesion kinase 1(Human)
Shenyang Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50619422(CHEMBL5396970)
Affinity DataIC50: 29nMAssay Description:Inhibition of FAK (unknown origin) incubated for 50 mins in presence of substrate/ATP by HTRF assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetFocal adhesion kinase 1(Human)
Shenyang Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50619417(CHEMBL5417189)
Affinity DataIC50: 32nMAssay Description:Inhibition of FAK (unknown origin) incubated for 50 mins in presence of substrate/ATP by HTRF assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetFocal adhesion kinase 1(Human)
Shenyang Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50619423(CHEMBL5431438)
Affinity DataIC50: 32nMAssay Description:Inhibition of FAK (unknown origin) incubated for 50 mins in presence of substrate/ATP by HTRF assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetFocal adhesion kinase 1(Human)
Shenyang Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50619405(CHEMBL5412700)
Affinity DataIC50: 119nMAssay Description:Inhibition of FAK (unknown origin) incubated for 50 mins in presence of substrate/ATP by HTRF assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetFocal adhesion kinase 1(Human)
Shenyang Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50619413(CHEMBL5421155)
Affinity DataIC50: 149nMAssay Description:Inhibition of FAK (unknown origin) incubated for 50 mins in presence of substrate/ATP by HTRF assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetFocal adhesion kinase 1(Human)
Shenyang Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50619406(CHEMBL5405166)
Affinity DataIC50: 163nMAssay Description:Inhibition of FAK (unknown origin) incubated for 50 mins in presence of substrate/ATP by HTRF assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetFocal adhesion kinase 1(Human)
Shenyang Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50619402(CHEMBL5414360)
Affinity DataIC50: 240nMAssay Description:Inhibition of FAK (unknown origin) incubated for 50 mins in presence of substrate/ATP by HTRF assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetFocal adhesion kinase 1(Human)
Shenyang Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50619401(CHEMBL5425967)
Affinity DataIC50: 328nMAssay Description:Inhibition of FAK (unknown origin) incubated for 50 mins in presence of substrate/ATP by HTRF assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetFocal adhesion kinase 1(Human)
Shenyang Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50619400(CHEMBL5422250)
Affinity DataIC50: 356nMAssay Description:Inhibition of FAK (unknown origin) incubated for 50 mins in presence of substrate/ATP by HTRF assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetFocal adhesion kinase 1(Human)
Shenyang Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50619403(CHEMBL5431011)
Affinity DataIC50: 361nMAssay Description:Inhibition of FAK (unknown origin) incubated for 50 mins in presence of substrate/ATP by HTRF assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetFocal adhesion kinase 1(Human)
Shenyang Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50619404(CHEMBL5402091)
Affinity DataIC50: 413nMAssay Description:Inhibition of FAK (unknown origin) incubated for 50 mins in presence of substrate/ATP by HTRF assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed