BDBM50287097 4-Methyl-N*3*-(4-pyridin-3-yl-pyrimidin-2-yl)-benzene-1,3-diamine::CHEMBL278103

SMILES Cc1ccc(N)cc1Nc1nccc(n1)-c1cccnc1

InChI Key InChIKey=QGAIPGVQJVGBIA-UHFFFAOYSA-N

Data  15 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 15 hits for monomerid = 50287097   

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

Curated by ChEMBL
LigandPNGBDBM50287097(4-Methyl-N*3*-(4-pyridin-3-yl-pyrimidin-2-yl)-benz...)
Affinity DataIC50:  2.40E+5nMAssay Description:Inhibition of protein kinase C alpha.More data for this Ligand-Target Pair
In DepthDetails Article
TargetHeme oxygenase 1(Rattus norvegicus (rat))
University Of Catania

Curated by ChEMBL
LigandPNGBDBM50287097(4-Methyl-N*3*-(4-pyridin-3-yl-pyrimidin-2-yl)-benz...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of heme oxygenase 1 in Sprague-Dawley rat spleen microsomal fraction assessed as decrease in bilirubin formation using biliverdin reductas...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein kinase C delta type(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50287097(4-Methyl-N*3*-(4-pyridin-3-yl-pyrimidin-2-yl)-benz...)
Affinity DataIC50: >5.00E+5nMAssay 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
LigandPNGBDBM50287097(4-Methyl-N*3*-(4-pyridin-3-yl-pyrimidin-2-yl)-benz...)
Affinity DataIC50: >1.00E+5nMAssay 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
LigandPNGBDBM50287097(4-Methyl-N*3*-(4-pyridin-3-yl-pyrimidin-2-yl)-benz...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of c-Src-tyrosine kinase.More data for this Ligand-Target Pair
In DepthDetails Article
TargetTyrosine-protein kinase ABL1(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50287097(4-Methyl-N*3*-(4-pyridin-3-yl-pyrimidin-2-yl)-benz...)
Affinity DataIC50:  1.50E+3nMAssay Description:Inhibition of v-Abl tyrosine kinase.More data for this Ligand-Target Pair
In DepthDetails Article
TargetEpidermal growth factor receptor(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50287097(4-Methyl-N*3*-(4-pyridin-3-yl-pyrimidin-2-yl)-benz...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of tyrosine kinase Epidermal growth factor receptorMore data for this Ligand-Target Pair
In DepthDetails Article
TargetProtein kinase C delta type(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50287097(4-Methyl-N*3*-(4-pyridin-3-yl-pyrimidin-2-yl)-benz...)
Affinity DataIC50: >5.00E+5nMAssay Description:Inhibition of serine/threonine kinase(PKC-delta)More data for this Ligand-Target Pair
In DepthDetails Article
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50287097(4-Methyl-N*3*-(4-pyridin-3-yl-pyrimidin-2-yl)-benz...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of tyrosine kinase(c-Src)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
LigandPNGBDBM50287097(4-Methyl-N*3*-(4-pyridin-3-yl-pyrimidin-2-yl)-benz...)
Affinity DataIC50:  1.51E+3nMAssay Description:Inhibition of BCR-ABL kinase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50287097(4-Methyl-N*3*-(4-pyridin-3-yl-pyrimidin-2-yl)-benz...)
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))
TBA

Curated by ChEMBL
LigandPNGBDBM50287097(4-Methyl-N*3*-(4-pyridin-3-yl-pyrimidin-2-yl)-benz...)
Affinity DataIC50: >1.00E+4nMAssay 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))
TBA

Curated by ChEMBL
LigandPNGBDBM50287097(4-Methyl-N*3*-(4-pyridin-3-yl-pyrimidin-2-yl)-benz...)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of the platelet-derived growth factor receptor.More data for this Ligand-Target Pair
In DepthDetails Article
LigandPNGBDBM50287097(4-Methyl-N*3*-(4-pyridin-3-yl-pyrimidin-2-yl)-benz...)
Affinity DataIC50: >5.00E+5nMAssay Description:Inhibition of protein kinase A.More data for this Ligand-Target Pair
In DepthDetails Article
TargetProtein kinase C alpha type(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50287097(4-Methyl-N*3*-(4-pyridin-3-yl-pyrimidin-2-yl)-benz...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of serine/threonine kinase(PKC-alpha)More data for this Ligand-Target Pair
In DepthDetails Article