BDBM50175493 CHEMBL277931::N-[3-(4-Pyridin-3-yl-pyrimidin-2-ylamino)-phenyl]-benzamide

SMILES O=C(Nc1cccc(Nc2nccc(n2)-c2cccnc2)c1)c1ccccc1

InChI Key InChIKey=ZVXCXEJBPDCMRL-UHFFFAOYSA-N

Data  18 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 18 hits for monomerid = 50175493   

TargetProtein kinase C alpha type(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50175493(CHEMBL277931 | N-[3-(4-Pyridin-3-yl-pyrimidin-2-yl...)
Affinity DataIC50:  1.20E+3nMAssay Description:Inhibition of protein kinase C alpha.More data for this Ligand-Target Pair
In DepthDetails Article
LigandPNGBDBM50175493(CHEMBL277931 | N-[3-(4-Pyridin-3-yl-pyrimidin-2-yl...)
Affinity DataIC50: >5.00E+5nMAssay Description:Inhibition of protein kinase A.More data for this Ligand-Target Pair
In DepthDetails Article
TargetPlatelet-derived growth factor receptor alpha/beta(Homo sapiens (Human))
Organon Laboratories

Curated by ChEMBL
LigandPNGBDBM50175493(CHEMBL277931 | N-[3-(4-Pyridin-3-yl-pyrimidin-2-yl...)
Affinity DataIC50:  5.00E+3nMAssay Description:Inhibitory concentration against platelet-derived growth factor receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein kinase C alpha type(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50175493(CHEMBL277931 | N-[3-(4-Pyridin-3-yl-pyrimidin-2-yl...)
Affinity DataIC50:  1.20E+3nMAssay Description:Inhibitory concentration against protein kinase C alphaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase ABL1(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50175493(CHEMBL277931 | N-[3-(4-Pyridin-3-yl-pyrimidin-2-yl...)
Affinity DataIC50:  400nMAssay Description:Inhibition of v-Abl tyrosine kinase.More data for this Ligand-Target Pair
In DepthDetails Article
TargetProtein kinase C delta type(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50175493(CHEMBL277931 | N-[3-(4-Pyridin-3-yl-pyrimidin-2-yl...)
Affinity DataIC50:  2.30E+4nMAssay Description:Inhibition of protein kinase C delta.More data for this Ligand-Target Pair
In DepthDetails Article
TargetEpidermal growth factor receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50175493(CHEMBL277931 | N-[3-(4-Pyridin-3-yl-pyrimidin-2-yl...)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of the epidermal growth factor receptor.More data for this Ligand-Target Pair
In DepthDetails Article
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50175493(CHEMBL277931 | N-[3-(4-Pyridin-3-yl-pyrimidin-2-yl...)
Affinity DataIC50:  1.57E+4nMAssay Description:Inhibition of c-Src-tyrosine kinase.More data for this Ligand-Target Pair
In DepthDetails Article
TargetEpidermal growth factor receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50175493(CHEMBL277931 | N-[3-(4-Pyridin-3-yl-pyrimidin-2-yl...)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of tyrosine kinase Epidermal growth factor receptorMore data for this Ligand-Target Pair
In DepthDetails Article
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50175493(CHEMBL277931 | N-[3-(4-Pyridin-3-yl-pyrimidin-2-yl...)
Affinity DataIC50:  1.57E+4nMAssay Description:Inhibition of tyrosine kinase(c-Src)More data for this Ligand-Target Pair
In DepthDetails Article
TargetProtein kinase C delta type(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50175493(CHEMBL277931 | N-[3-(4-Pyridin-3-yl-pyrimidin-2-yl...)
Affinity DataIC50:  2.30E+4nMAssay Description:Inhibition of serine/threonine kinase(PKC-delta)More data for this Ligand-Target Pair
In DepthDetails Article
TargetTyrosine-protein kinase ABL1(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50175493(CHEMBL277931 | N-[3-(4-Pyridin-3-yl-pyrimidin-2-yl...)
Affinity DataIC50:  400nMAssay Description:Inhibitory concentration against v-Abl tyrosine kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50175493(CHEMBL277931 | N-[3-(4-Pyridin-3-yl-pyrimidin-2-yl...)
Affinity DataIC50:  1.57E+4nMAssay Description:Inhibitory concentration against Src kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBreakpoint cluster region protein/Tyrosine-protein kinase ABL1(Homo sapiens (Human))
The First People'S Hospital Of Hangzhou

Curated by ChEMBL
LigandPNGBDBM50175493(CHEMBL277931 | N-[3-(4-Pyridin-3-yl-pyrimidin-2-yl...)
Affinity DataIC50:  398nMAssay Description:Inhibition of BCR-ABL kinase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlatelet-derived growth factor receptor alpha/beta(Homo sapiens (Human))
Organon Laboratories

Curated by ChEMBL
LigandPNGBDBM50175493(CHEMBL277931 | N-[3-(4-Pyridin-3-yl-pyrimidin-2-yl...)
Affinity DataIC50:  5.00E+3nMAssay Description:Inhibition of tyrosine kinase(PDGF-R)More data for this Ligand-Target Pair
In DepthDetails Article
LigandPNGBDBM50175493(CHEMBL277931 | N-[3-(4-Pyridin-3-yl-pyrimidin-2-yl...)
Affinity DataIC50: >5.00E+5nMAssay Description:Inhibition of tyrosine kinase(PDGF-R)More data for this Ligand-Target Pair
In DepthDetails Article
TargetPlatelet-derived growth factor receptor alpha/beta(Homo sapiens (Human))
Organon Laboratories

Curated by ChEMBL
LigandPNGBDBM50175493(CHEMBL277931 | N-[3-(4-Pyridin-3-yl-pyrimidin-2-yl...)
Affinity DataIC50:  5.00E+3nMAssay Description:Inhibition of the platelet-derived growth factor receptor.More data for this Ligand-Target Pair
In DepthDetails Article
TargetProtein kinase C alpha type(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50175493(CHEMBL277931 | N-[3-(4-Pyridin-3-yl-pyrimidin-2-yl...)
Affinity DataIC50:  1.20E+3nMAssay Description:Inhibition of serine/threonine kinase(PKC-alpha)More data for this Ligand-Target Pair
In DepthDetails Article