BDBM50045528 CHEMBL57553::N-(4-Pyridin-3-yl-pyrimidin-2-yl)-benzene-1,3-diamine

SMILES Nc1cccc(Nc2nccc(n2)-c2cccnc2)c1

InChI Key InChIKey=ZQTRXPRIWRFHRY-UHFFFAOYSA-N

Data  9 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 9 hits for monomerid = 50045528   

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

Curated by ChEMBL
LigandPNGBDBM50045528(CHEMBL57553 | N-(4-Pyridin-3-yl-pyrimidin-2-yl)-be...)
Affinity DataIC50:  2.10E+5nMAssay Description:Inhibition of protein kinase C alpha.More data for this Ligand-Target Pair
In DepthDetails Article
TargetEpidermal growth factor receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50045528(CHEMBL57553 | N-(4-Pyridin-3-yl-pyrimidin-2-yl)-be...)
Affinity DataIC50:  5.00E+4nMAssay Description:Inhibition of the epidermal growth factor receptor.More data for this Ligand-Target Pair
In DepthDetails Article
TargetProtein kinase C delta type(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50045528(CHEMBL57553 | N-(4-Pyridin-3-yl-pyrimidin-2-yl)-be...)
Affinity DataIC50: >5.00E+5nMAssay Description:Inhibition of protein kinase C delta.More data for this Ligand-Target Pair
In DepthDetails Article
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50045528(CHEMBL57553 | N-(4-Pyridin-3-yl-pyrimidin-2-yl)-be...)
Affinity DataIC50:  1.40E+4nMAssay Description:Inhibition of c-Src-tyrosine kinase.More data for this Ligand-Target Pair
In DepthDetails Article
TargetPlatelet-derived growth factor receptor alpha/beta(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50045528(CHEMBL57553 | N-(4-Pyridin-3-yl-pyrimidin-2-yl)-be...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of the platelet-derived growth factor receptor.More data for this Ligand-Target Pair
In DepthDetails Article
TargetBreakpoint cluster region protein/Tyrosine-protein kinase ABL1(Homo sapiens (Human))
The First People'S Hospital Of Hangzhou

Curated by ChEMBL
LigandPNGBDBM50045528(CHEMBL57553 | N-(4-Pyridin-3-yl-pyrimidin-2-yl)-be...)
Affinity DataIC50:  708nMAssay Description:Inhibition of BCR-ABL kinase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase ABL1/ABL2(Homo sapiens (Human))
Mcgill University/Royal Victoria Hospital

Curated by ChEMBL
LigandPNGBDBM50045528(CHEMBL57553 | N-(4-Pyridin-3-yl-pyrimidin-2-yl)-be...)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of Abl tyrosine kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50045528(CHEMBL57553 | N-(4-Pyridin-3-yl-pyrimidin-2-yl)-be...)
Affinity DataIC50:  6.00E+3nMAssay Description:Inhibition of the platelet-derived growth factor receptor.More data for this Ligand-Target Pair
In DepthDetails Article
TargetTyrosine-protein kinase ABL1(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50045528(CHEMBL57553 | N-(4-Pyridin-3-yl-pyrimidin-2-yl)-be...)
Affinity DataIC50:  700nMAssay Description:Inhibition of v-Abl tyrosine kinase.More data for this Ligand-Target Pair
In DepthDetails Article