BDBM50425667 CHEMBL2315583

SMILES CN(c1ncccc1CNc1c(cnc2[nH]c(cc12)-c1ccnc(C)c1)C#N)S(C)(=O)=O

InChI Key InChIKey=UPABBOVWARPMGK-UHFFFAOYSA-N

Data  2 IC50  1 Kd

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50425667   

TargetFocal adhesion kinase 1(Homo sapiens (Human))
Merck Serono

Curated by ChEMBL
LigandPNGBDBM50425667(CHEMBL2315583)
Affinity DataIC50:  6.50E+3nMAssay Description:Inhibition of FAK in human HT-29 cells assessed as phosphorylation at tyrosine 397 after 45 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFocal adhesion kinase 1(Homo sapiens (Human))
Merck Serono

Curated by ChEMBL
LigandPNGBDBM50425667(CHEMBL2315583)
Affinity DataKd:  24nMAssay Description:Binding affinity to FAK (unknown origin) by surface plasmon resonance analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFocal adhesion kinase 1(Homo sapiens (Human))
Merck Serono

Curated by ChEMBL
LigandPNGBDBM50425667(CHEMBL2315583)
Affinity DataIC50:  220nMAssay Description:Inhibition of FAK (unknown origin) using biotinylated His-TEV-hsFAK(31-686)(K454R) substrate after 2 hrs by scintillation counting analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed