BDBM50379366 CHEMBL2011944

SMILES COc1ccccc1-c1nc2ncc(Br)c(NCC(O)CNC(=O)C3CCC3)c2[nH]1

InChI Key InChIKey=QKAVQJBBCRMGMX-UHFFFAOYSA-N

Data  4 IC50  1 EC50

  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 5 hits for monomerid = 50379366   

TargetAurora kinase B(Human)
Astrazeneca R&D Boston

Curated by ChEMBL
LigandPNGBDBM50379366(CHEMBL2011944)
Affinity DataIC50: 872nMAssay Description:Inhibition of Aurora B kinaseMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetSerine/threonine-protein kinase TBK1(Human)
Astrazeneca R&D Boston

Curated by ChEMBL
LigandPNGBDBM50379366(CHEMBL2011944)
Affinity DataEC50:  35nMAssay Description:Inhibition of TBK1-mediated NFkappaB activation expressed in ds-RNA activated HEK293 cells coexpressing TLR3 after 4.5 hrs by luciferase reporter gen...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetSerine/threonine-protein kinase TBK1(Human)
Astrazeneca R&D Boston

Curated by ChEMBL
LigandPNGBDBM50379366(CHEMBL2011944)
Affinity DataIC50: 32nMAssay Description:Inhibition of recombinant TBK1 using 5FAM-AhxKRRAL(ps)VASLPGL as substrate by microfluidic mobility shift assayMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetInhibitor of nuclear factor kappa-B kinase subunit epsilon(Human)
Astrazeneca R&D Boston

Curated by ChEMBL
LigandPNGBDBM50379366(CHEMBL2011944)
Affinity DataIC50: 102nMAssay Description:Inhibition of Ikkepsilon using 5FAM-AKELDQGSLCTpSFVGTLQ-NH2 as substrate by microfluidic mobility shift assayMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCyclin-dependent kinase 2(Human)
Astrazeneca R&D Boston

Curated by ChEMBL
LigandPNGBDBM50379366(CHEMBL2011944)
Affinity DataIC50: 4.65E+3nMAssay Description:Inhibition of CDK2More data for this Ligand-Target Pair
In DepthDetails Article
PubMed