Compile Data Set for Download or QSAR
Report error Found 54 Enz. Inhib. hit(s) with all data for entry = 50017425
TargetFocal adhesion kinase 1(Human)
Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50182013BDBM50182013(5-bromo-N4-(pyridin-2-yl)-N2-(3,4,5-trimethoxyphen...)
Affinity DataIC50: 100nMAssay Description:Inhibitory activity against FAKMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetFocal adhesion kinase 1(Human)
Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50181998BDBM50181998(7-(pyridin-3-yl)-N-(3,4,5-trimethoxyphenyl)-7H-pyr...)
Affinity DataIC50: 100nMAssay Description:Inhibitory activity against FAKMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetFocal adhesion kinase 1(Human)
Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50182014BDBM50182014(7-(pyridin-2-yl)-N-(3,4,5-trimethoxyphenyl)-6,7-di...)
Affinity DataIC50: 100nMAssay Description:Inhibitory activity against FAKMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetFocal adhesion kinase 1(Human)
Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50182010BDBM50182010(7-(pyridin-2-yl)-N-(2,4,6-trimethoxyphenyl)-7H-pyr...)
Affinity DataIC50: 200nMAssay Description:Inhibitory activity against FAKMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetFocal adhesion kinase 1(Human)
Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50181975BDBM50181975(8-(pyridin-2-yl)-N-(3,4,5-trimethoxyphenyl)-5,6,7,...)
Affinity DataIC50: 200nMAssay Description:Inhibitory activity against FAKMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetFocal adhesion kinase 1(Human)
Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50181983BDBM50181983(N-(5-methoxy-2-methylphenyl)-7-(pyridin-2-yl)-7H-p...)
Affinity DataIC50: 200nMAssay Description:Inhibitory activity against FAKMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetFocal adhesion kinase 1(Human)
Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50182006BDBM50182006(8-(pyridin-2-yl)-2-(3,4,5-trimethoxyphenylamino)-5...)
Affinity DataIC50: 200nMAssay Description:Inhibitory activity against FAKMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetFocal adhesion kinase 1(Human)
Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50181987BDBM50181987(ethyl 2-(4-(pyridin-2-ylamino)-2-(3,4,5-trimethoxy...)
Affinity DataIC50: 200nMAssay Description:Inhibitory activity against FAKMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetFocal adhesion kinase 1(Human)
Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50181979BDBM50181979(7-(4-methoxypyridin-3-yl)-N-(3,4,5-trimethoxypheny...)
Affinity DataIC50: 300nMAssay Description:Inhibitory activity against FAKMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetFocal adhesion kinase 1(Human)
Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50181968BDBM50181968(7-(pyridin-2-yl)-N-(5,6,7,8-tetrahydronaphthalen-1...)
Affinity DataIC50: 300nMAssay Description:Inhibitory activity against FAKMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetFocal adhesion kinase 1(Human)
Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50182002BDBM50182002(4-methyl-3-(7-(pyridin-2-yl)-7H-pyrrolo[2,3-d]pyri...)
Affinity DataIC50: 400nMAssay Description:Inhibitory activity against FAKMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetFocal adhesion kinase 1(Human)
Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50181981BDBM50181981(7-(4-chloropyridin-3-yl)-N-(3,4,5-trimethoxyphenyl...)
Affinity DataIC50: 500nMAssay Description:Inhibitory activity against FAKMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetFocal adhesion kinase 1(Human)
Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50181999BDBM50181999(7-(thiazol-2-yl)-N-(3,4,5-trimethoxyphenyl)-7H-pyr...)
Affinity DataIC50: 500nMAssay Description:Inhibitory activity against FAKMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetFocal adhesion kinase 1(Human)
Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50181969BDBM50181969(7-(pyridin-2-yl)-N-o-tolyl-7H-pyrrolo[2,3-d]pyrimi...)
Affinity DataIC50: 500nMAssay Description:Inhibitory activity against FAKMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetFocal adhesion kinase 1(Human)
Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50181982BDBM50181982(N-(3-methoxyphenyl)-7-(pyridin-2-yl)-7H-pyrrolo[2,...)
Affinity DataIC50: 600nMAssay Description:Inhibitory activity against FAKMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetFocal adhesion kinase 1(Human)
Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50181986BDBM50181986(N-(2-methyl-5-(quinoxalin-2-yl)phenyl)-7-(pyridin-...)
Affinity DataIC50: 600nMAssay Description:Inhibitory activity against FAKMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetFocal adhesion kinase 1(Human)
Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50182015BDBM50182015(N-(2-methoxyphenyl)-7-(pyridin-2-yl)-7H-pyrrolo[2,...)
Affinity DataIC50: 700nMAssay Description:Inhibitory activity against FAKMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetFocal adhesion kinase 1(Human)
Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50182007BDBM50182007(7-(pyridin-2-yl)-N-m-tolyl-7H-pyrrolo[2,3-d]pyrimi...)
Affinity DataIC50: 700nMAssay Description:Inhibitory activity against FAKMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetFocal adhesion kinase 1(Human)
Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50182005BDBM50182005(N-(2-chlorophenyl)-7-(pyridin-2-yl)-7H-pyrrolo[2,3...)
Affinity DataIC50: 700nMAssay Description:Inhibitory activity against FAKMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetFocal adhesion kinase 1(Human)
Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50182012BDBM50182012(7-(4-fluoropyridin-3-yl)-N-(3,4,5-trimethoxyphenyl...)
Affinity DataIC50: 800nMAssay Description:Inhibitory activity against FAKMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetFocal adhesion kinase 1(Human)
Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50182018BDBM50182018(7-(2-chloropyrimidin-4-yl)-N-(3,4,5-trimethoxyphen...)
Affinity DataIC50: 800nMAssay Description:Inhibitory activity against FAKMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetFocal adhesion kinase 1(Human)
Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50181988BDBM50181988(7-(2-chloropyridin-4-yl)-N-(3,4,5-trimethoxyphenyl...)
Affinity DataIC50: 800nMAssay Description:Inhibitory activity against FAKMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetFocal adhesion kinase 1(Human)
Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50181994BDBM50181994(N-(2-ethylphenyl)-7-(pyridin-2-yl)-7H-pyrrolo[2,3-...)
Affinity DataIC50: 900nMAssay Description:Inhibitory activity against FAKMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetFocal adhesion kinase 1(Human)
Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50182009BDBM50182009(N-(2-(methylthio)phenyl)-7-(pyridin-2-yl)-7H-pyrro...)
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibitory activity against FAKMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetFocal adhesion kinase 1(Human)
Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50182019BDBM50182019(N-(2-fluorophenyl)-7-(pyridin-2-yl)-7H-pyrrolo[2,3...)
Affinity DataIC50: 1.20E+3nMAssay Description:Inhibitory activity against FAKMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetFocal adhesion kinase 1(Human)
Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50181977BDBM50181977(N-(2-bromophenyl)-7-(pyridin-2-yl)-7H-pyrrolo[2,3-...)
Affinity DataIC50: 1.50E+3nMAssay Description:Inhibitory activity against FAKMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetFocal adhesion kinase 1(Human)
Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50181966BDBM50181966(N-(3-(methylthio)phenyl)-7-(pyridin-2-yl)-7H-pyrro...)
Affinity DataIC50: 2.00E+3nMAssay Description:Inhibitory activity against FAKMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetFocal adhesion kinase 1(Human)
Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50181976BDBM50181976(N-(5-iodo-2-methylphenyl)-7-(pyridin-2-yl)-7H-pyrr...)
Affinity DataIC50: 3.00E+3nMAssay Description:Inhibitory activity against FAKMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetFocal adhesion kinase 1(Human)
Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50181973BDBM50181973(7-(pyridin-2-yl)-N-(2-(trifluoromethyl)phenyl)-7H-...)
Affinity DataIC50: 7.00E+3nMAssay Description:Inhibitory activity against FAKMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetFocal adhesion kinase 1(Human)
Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50182000BDBM50182000(7-(2-(pyridin-4-yl)ethyl)-N-(3,4,5-trimethoxypheny...)
Affinity DataIC50: 7.50E+3nMAssay Description:Inhibitory activity against FAKMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetFocal adhesion kinase 1(Human)
Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50181997BDBM50181997(7-(pyridin-3-ylmethyl)-N-(3,4,5-trimethoxyphenyl)-...)
Affinity DataIC50: 7.90E+3nMAssay Description:Inhibitory activity against FAKMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetFocal adhesion kinase 1(Human)
Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50181978BDBM50181978(N-(4-iodo-2-methylphenyl)-7-(pyridin-2-yl)-7H-pyrr...)
Affinity DataIC50: 8.00E+3nMAssay Description:Inhibitory activity against FAKMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetFocal adhesion kinase 1(Human)
Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50181990BDBM50181990(7-(pyridin-4-yl)-N-(3,4,5-trimethoxyphenyl)-7H-pyr...)
Affinity DataIC50: 9.00E+3nMAssay Description:Inhibitory activity against FAKMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetFocal adhesion kinase 1(Human)
Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50181989BDBM50181989(N-benzyl-7-(pyridin-2-yl)-7H-pyrrolo[2,3-d]pyrimid...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibitory activity against FAKMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetFocal adhesion kinase 1(Human)
Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50181991BDBM50181991((4-methyl-3-(7-(pyridin-2-yl)-7H-pyrrolo[2,3-d]pyr...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibitory activity against FAKMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetFocal adhesion kinase 1(Human)
Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50181992BDBM50181992(7-(4-chloropyrimidin-2-yl)-N-(3,4,5-trimethoxyphen...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibitory activity against FAKMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetFocal adhesion kinase 1(Human)
Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50181993BDBM50181993(1-(3-(7-(pyridin-2-yl)-7H-pyrrolo[2,3-d]pyrimidin-...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibitory activity against FAKMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetFocal adhesion kinase 1(Human)
Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50181996BDBM50181996(8-(pyridin-2-yl)-2-(3,4,5-trimethoxyphenylamino)py...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibitory activity against FAKMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetFocal adhesion kinase 1(Human)
Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50181995BDBM50181995(N-(3,4,5-trimethoxybenzyl)-7-(pyridin-2-yl)-7H-pyr...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibitory activity against FAKMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetFocal adhesion kinase 1(Human)
Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50181967BDBM50181967(8-(pyridin-2-yl)-2-(3,4,5-trimethoxyphenylamino)-5...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibitory activity against FAKMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetFocal adhesion kinase 1(Human)
Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50182001BDBM50182001(3-(7-(pyridin-2-yl)-7H-pyrrolo[2,3-d]pyrimidin-2-y...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibitory activity against FAKMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetFocal adhesion kinase 1(Human)
Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50181970BDBM50181970(7-(thiophen-2-yl)-N-(3,4,5-trimethoxyphenyl)-7H-py...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibitory activity against FAKMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetFocal adhesion kinase 1(Human)
Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50182004BDBM50182004(7-(pyridin-2-yl)-N-(4-(trifluoromethyl)phenyl)-7H-...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibitory activity against FAKMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetFocal adhesion kinase 1(Human)
Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50181971BDBM50181971(N-(benzo[d][1,3]dioxol-5-yl)-7-(pyridin-2-yl)-7H-p...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibitory activity against FAKMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetFocal adhesion kinase 1(Human)
Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50181972BDBM50181972(N-(2-methyl-5-nitrophenyl)-7-(pyridin-2-yl)-7H-pyr...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibitory activity against FAKMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetFocal adhesion kinase 1(Human)
Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50182003BDBM50182003(7-(2-(pyridin-3-yl)ethyl)-N-(3,4,5-trimethoxypheny...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibitory activity against FAKMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetFocal adhesion kinase 1(Human)
Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50181974BDBM50181974(N-(1H-indol-6-yl)-7-(pyridin-2-yl)-7H-pyrrolo[2,3-...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibitory activity against FAKMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetFocal adhesion kinase 1(Human)
Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50182008BDBM50182008(N-(5-bromo-2-methylphenyl)-7-(pyridin-2-yl)-7H-pyr...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibitory activity against FAKMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetFocal adhesion kinase 1(Human)
Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50182011BDBM50182011(ethyl 2-(4-chloro-2-(3,4,5-trimethoxyphenylamino)p...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibitory activity against FAKMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetFocal adhesion kinase 1(Human)
Genomics Institute of The Novartis Research Foundation

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50181980BDBM50181980(2-(4-methylpiperazin-1-yl)-7-(pyridin-2-yl)-7H-pyr...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibitory activity against FAKMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
Displayed 1 to 50 (of 54 total ) | Next | Last >>
Jump to: