BDBM50425672 CHEMBL2315584

SMILES CN(c1ncccc1CNc1c(cnc2[nH]c(cc12)-c1ccc(F)cc1)C(F)(F)F)S(C)(=O)=O

InChI Key InChIKey=UCQJUBOMLHYQTJ-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 = 50425672   

TargetFocal adhesion kinase 1(Human)
Merck Serono

Curated by ChEMBL
LigandPNGBDBM50425672(CHEMBL2315584)
Affinity DataIC50:  2.02E+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(Human)
Merck Serono

Curated by ChEMBL
LigandPNGBDBM50425672(CHEMBL2315584)
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(Human)
Merck Serono

Curated by ChEMBL
LigandPNGBDBM50425672(CHEMBL2315584)
Affinity DataIC50:  37nMAssay 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