BDBM50614163 CHEMBL5288779

SMILES c1ccc(cc1)CNc2c3c(cncn3)c4ccc(cc4n2)C(=O)O

InChI Key InChIKey=HEVVNKYNJCSHFA-UHFFFAOYSA-N

Data  15 IC50

PDB links: 1 PDB ID matches this monomer.

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 15 hits for monomerid = 50614163   

TargetCasein kinase II subunit alpha(Human)
University of North Carolina At Chapel Hill

Curated by ChEMBL
LigandPNGBDBM50614163(CHEMBL5288779)
Affinity DataIC50: 920nMAssay Description:Inhibition of C-terminal Nano-Luc fused human CK2alpha expressed in HEK293 cells using NanoBRET NanoGlo substrate in presence of tracer K10 by NanoBR...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/22/2024
Entry Details
PubMedPDB3D3D Structure (crystal)
TargetCasein kinase II subunit alpha'(Human)
University of North Carolina At Chapel Hill

Curated by ChEMBL
LigandPNGBDBM50614163(CHEMBL5288779)
Affinity DataIC50: 200nMAssay Description:Inhibition of C-terminal Nano-Luc fused human CK2alpha' expressed in HEK293 cells using NanoBRET NanoGlo substrate in presence of tracer K5 by NanoBR...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/22/2024
Entry Details
PubMedPDB3D3D Structure (crystal)
TargetCasein kinase II subunit alpha(Human)
University of North Carolina At Chapel Hill

Curated by ChEMBL
LigandPNGBDBM50614163(CHEMBL5288779)
Affinity DataIC50: 3.00E+3nMAssay Description:Inhibition of wild type human CK2alpha in presence of ATP by radiometric kinase assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/22/2024
Entry Details
PubMedPDB3D3D Structure (crystal)
TargetCasein kinase II subunit alpha'(Human)
University of North Carolina At Chapel Hill

Curated by ChEMBL
LigandPNGBDBM50614163(CHEMBL5288779)
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of wild type human CK2alpha' in presence of ATP by radiometric kinase assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/22/2024
Entry Details
PubMedPDB3D3D Structure (crystal)
TargetDeath-associated protein kinase 3(Human)
University of North Carolina At Chapel Hill

Curated by ChEMBL
LigandPNGBDBM50614163(CHEMBL5288779)
Affinity DataIC50: 1.50E+6nMAssay Description:Inhibition of wild type human DAPK3 in presence of ATP by radiometric kinase assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/22/2024
Entry Details
PubMed
TargetHomeodomain-interacting protein kinase 1(Human)
University of North Carolina At Chapel Hill

Curated by ChEMBL
LigandPNGBDBM50614163(CHEMBL5288779)
Affinity DataIC50: 1.80E+6nMAssay Description:Inhibition of wild type human HIPK1 in presence of ATP by radiometric kinase assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/22/2024
Entry Details
PubMed
TargetDeath-associated protein kinase 2(Human)
University of North Carolina At Chapel Hill

Curated by ChEMBL
LigandPNGBDBM50614163(CHEMBL5288779)
Affinity DataIC50: 1.50E+6nMAssay Description:Inhibition of wild type human DAPK2 in presence of ATP by radiometric kinase assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/22/2024
Entry Details
PubMed
TargetHomeodomain-interacting protein kinase 3(Human)
University of North Carolina At Chapel Hill

Curated by ChEMBL
LigandPNGBDBM50614163(CHEMBL5288779)
Affinity DataIC50: 9.00E+5nMAssay Description:Inhibition of wild type human HIPK3 in presence of ATP by radiometric kinase assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/22/2024
Entry Details
PubMed
TargetMyosin light chain kinase family member 4(Human)
University of North Carolina At Chapel Hill

Curated by ChEMBL
LigandPNGBDBM50614163(CHEMBL5288779)
Affinity DataIC50: 1.00E+7nMAssay Description:Inhibition of wild type human MYLK4 in presence of ATP by radiometric kinase assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/22/2024
Entry Details
PubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform(Human)
University of North Carolina At Chapel Hill

Curated by ChEMBL
LigandPNGBDBM50614163(CHEMBL5288779)
Affinity DataIC50: 5.30E+6nMAssay Description:Inhibition of wild type human PIK3CG in presence of ATP by radiometric kinase assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/22/2024
Entry Details
PubMed
TargetPhosphatidylinositol 3-kinase C2 domain-containing subunit gamma(Human)
University of North Carolina At Chapel Hill

Curated by ChEMBL
LigandPNGBDBM50614163(CHEMBL5288779)
Affinity DataIC50: 4.50E+6nMAssay Description:Inhibition of wild type human PIK3C2G in presence of ATP by radiometric kinase assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/22/2024
Entry Details
PubMed
TargetDual specificity tyrosine-phosphorylation-regulated kinase 1A(Human)
University of North Carolina At Chapel Hill

Curated by ChEMBL
LigandPNGBDBM50614163(CHEMBL5288779)
Affinity DataIC50: 7.60E+5nMAssay Description:Inhibition of wild type human DYRK1A in presence of ATP by radiometric kinase assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/22/2024
Entry Details
PubMed
TargetHomeodomain-interacting protein kinase 2(Human)
University of North Carolina At Chapel Hill

Curated by ChEMBL
LigandPNGBDBM50614163(CHEMBL5288779)
Affinity DataIC50: 6.00E+5nMAssay Description:Inhibition of wild type human HIPK2 in presence of ATP by radiometric kinase assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/22/2024
Entry Details
PubMed
TargetSerine/threonine-protein kinase 17B(Human)
University of North Carolina At Chapel Hill

Curated by ChEMBL
LigandPNGBDBM50614163(CHEMBL5288779)
Affinity DataIC50: 2.80E+6nMAssay Description:Inhibition of wild type human DRAK2 in presence of ATP by radiometric kinase assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/22/2024
Entry Details
PubMed
TargetMitogen-activated protein kinase kinase kinase 19(Human)
University of North Carolina At Chapel Hill

Curated by ChEMBL
LigandPNGBDBM50614163(CHEMBL5288779)
Affinity DataIC50: 3.70E+6nMAssay Description:Inhibition of wild type human YSK4 in presence of ATP by radiometric kinase assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/22/2024
Entry Details
PubMed