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BDBM50290429 2-Methoxy-N-[3-(4-pyridin-3-yl-pyrimidin-2-ylamino)-phenyl]-benzamide::CHEMBL299707

SMILES: COc1ccccc1C(=O)Nc1cccc(Nc2nccc(n2)-c2cccnc2)c1

InChI Key: InChIKey=BSFVNTMWZAAILN-UHFFFAOYSA-N

Data: 8 IC50

Find this compound or compounds like it in BindingDB or PDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 8 hits for monomerid = 50290429   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kcal/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Protein kinase C alpha type


(Homo sapiens (Human))
BDBM50290429
PNG
(2-Methoxy-N-[3-(4-pyridin-3-yl-pyrimidin-2-ylamino...)
Show SMILES COc1ccccc1C(=O)Nc1cccc(Nc2nccc(n2)-c2cccnc2)c1
Show InChI InChI=1S/C23H19N5O2/c1-30-21-10-3-2-9-19(21)22(29)26-17-7-4-8-18(14-17)27-23-25-13-11-20(28-23)16-6-5-12-24-15-16/h2-15H,1H3,(H,26,29)(H,25,27,28)
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Article
n/an/a 320n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibition of protein kinase C alpha.


Bioorg Med Chem Lett 7: 187-192 (1997)


Article DOI: 10.1016/S0960-894X(96)00601-4
BindingDB Entry DOI: 10.7270/Q23X86MF
More data for this
Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))
BDBM50290429
PNG
(2-Methoxy-N-[3-(4-pyridin-3-yl-pyrimidin-2-ylamino...)
Show SMILES COc1ccccc1C(=O)Nc1cccc(Nc2nccc(n2)-c2cccnc2)c1
Show InChI InChI=1S/C23H19N5O2/c1-30-21-10-3-2-9-19(21)22(29)26-17-7-4-8-18(14-17)27-23-25-13-11-20(28-23)16-6-5-12-24-15-16/h2-15H,1H3,(H,26,29)(H,25,27,28)
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n/an/a>1.00E+5n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibition of c-Src-tyrosine kinase.


Bioorg Med Chem Lett 7: 187-192 (1997)


Article DOI: 10.1016/S0960-894X(96)00601-4
BindingDB Entry DOI: 10.7270/Q23X86MF
More data for this
Ligand-Target Pair
Protein kinase C delta type


(Homo sapiens (Human))
BDBM50290429
PNG
(2-Methoxy-N-[3-(4-pyridin-3-yl-pyrimidin-2-ylamino...)
Show SMILES COc1ccccc1C(=O)Nc1cccc(Nc2nccc(n2)-c2cccnc2)c1
Show InChI InChI=1S/C23H19N5O2/c1-30-21-10-3-2-9-19(21)22(29)26-17-7-4-8-18(14-17)27-23-25-13-11-20(28-23)16-6-5-12-24-15-16/h2-15H,1H3,(H,26,29)(H,25,27,28)
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n/an/a>5.00E+5n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibition of protein kinase C delta.


Bioorg Med Chem Lett 7: 187-192 (1997)


Article DOI: 10.1016/S0960-894X(96)00601-4
BindingDB Entry DOI: 10.7270/Q23X86MF
More data for this
Ligand-Target Pair
PDGFR-beta/Platelet-derived growth factor receptor alpha


(Homo sapiens (Human))
BDBM50290429
PNG
(2-Methoxy-N-[3-(4-pyridin-3-yl-pyrimidin-2-ylamino...)
Show SMILES COc1ccccc1C(=O)Nc1cccc(Nc2nccc(n2)-c2cccnc2)c1
Show InChI InChI=1S/C23H19N5O2/c1-30-21-10-3-2-9-19(21)22(29)26-17-7-4-8-18(14-17)27-23-25-13-11-20(28-23)16-6-5-12-24-15-16/h2-15H,1H3,(H,26,29)(H,25,27,28)
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n/an/a 1.00E+3n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibition of the platelet-derived growth factor receptor.


Bioorg Med Chem Lett 7: 187-192 (1997)


Article DOI: 10.1016/S0960-894X(96)00601-4
BindingDB Entry DOI: 10.7270/Q23X86MF
More data for this
Ligand-Target Pair
Tyrosine-protein kinase ABL1


(Homo sapiens (Human))
BDBM50290429
PNG
(2-Methoxy-N-[3-(4-pyridin-3-yl-pyrimidin-2-ylamino...)
Show SMILES COc1ccccc1C(=O)Nc1cccc(Nc2nccc(n2)-c2cccnc2)c1
Show InChI InChI=1S/C23H19N5O2/c1-30-21-10-3-2-9-19(21)22(29)26-17-7-4-8-18(14-17)27-23-25-13-11-20(28-23)16-6-5-12-24-15-16/h2-15H,1H3,(H,26,29)(H,25,27,28)
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n/an/a 1.90E+3n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibition of v-Abl tyrosine kinase.


Bioorg Med Chem Lett 7: 187-192 (1997)


Article DOI: 10.1016/S0960-894X(96)00601-4
BindingDB Entry DOI: 10.7270/Q23X86MF
More data for this
Ligand-Target Pair
Bcr-Abl


(Homo sapiens (Human))
BDBM50290429
PNG
(2-Methoxy-N-[3-(4-pyridin-3-yl-pyrimidin-2-ylamino...)
Show SMILES COc1ccccc1C(=O)Nc1cccc(Nc2nccc(n2)-c2cccnc2)c1
Show InChI InChI=1S/C23H19N5O2/c1-30-21-10-3-2-9-19(21)22(29)26-17-7-4-8-18(14-17)27-23-25-13-11-20(28-23)16-6-5-12-24-15-16/h2-15H,1H3,(H,26,29)(H,25,27,28)
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Article
PubMed
n/an/a 1.91E+3n/an/an/an/an/an/a



The First People's Hospital of Hangzhou

Curated by ChEMBL


Assay Description
Inhibition of BCR-ABL kinase (unknown origin)


Bioorg Med Chem Lett 23: 2442-50 (2013)


Article DOI: 10.1016/j.bmcl.2013.01.113
BindingDB Entry DOI: 10.7270/Q2ZG6TMD
More data for this
Ligand-Target Pair
cAMP-dependent protein kinase (PKA)


(Homo sapiens (Human))
BDBM50290429
PNG
(2-Methoxy-N-[3-(4-pyridin-3-yl-pyrimidin-2-ylamino...)
Show SMILES COc1ccccc1C(=O)Nc1cccc(Nc2nccc(n2)-c2cccnc2)c1
Show InChI InChI=1S/C23H19N5O2/c1-30-21-10-3-2-9-19(21)22(29)26-17-7-4-8-18(14-17)27-23-25-13-11-20(28-23)16-6-5-12-24-15-16/h2-15H,1H3,(H,26,29)(H,25,27,28)
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Article
n/an/a>5.00E+5n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibition of the platelet-derived growth factor receptor.


Bioorg Med Chem Lett 7: 187-192 (1997)


Article DOI: 10.1016/S0960-894X(96)00601-4
BindingDB Entry DOI: 10.7270/Q23X86MF
More data for this
Ligand-Target Pair
Epidermal growth factor receptor


(Homo sapiens (Human))
BDBM50290429
PNG
(2-Methoxy-N-[3-(4-pyridin-3-yl-pyrimidin-2-ylamino...)
Show SMILES COc1ccccc1C(=O)Nc1cccc(Nc2nccc(n2)-c2cccnc2)c1
Show InChI InChI=1S/C23H19N5O2/c1-30-21-10-3-2-9-19(21)22(29)26-17-7-4-8-18(14-17)27-23-25-13-11-20(28-23)16-6-5-12-24-15-16/h2-15H,1H3,(H,26,29)(H,25,27,28)
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n/an/a 1.00E+5n/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Inhibition of the epidermal growth factor receptor.


Bioorg Med Chem Lett 7: 187-192 (1997)


Article DOI: 10.1016/S0960-894X(96)00601-4
BindingDB Entry DOI: 10.7270/Q23X86MF
More data for this
Ligand-Target Pair