Found 90 hits of Enzyme Inhibition Constant Data Target/Host
(Institution) | Ligand | Target/Host
Links | Ligand
Links | Trg + Lig
Links | Ki
nM | ΔG°
kJ/mole | IC50
nM | Kd
nM | EC50/IC50
nM | koff
s-1 | kon
M-1s-1 | pH | Temp
°C |
|---|
Platelet-derived growth factor receptor alpha/beta
(Homo sapiens (Human)) | BDBM50287090
(4-Chloro-N-[4-methyl-3-(4-pyridin-3-yl-pyrimidin-2...)Show SMILES Cc1ccc(NC(=O)c2ccc(Cl)cc2)cc1Nc1nccc(n1)-c1cccnc1 Show InChI InChI=1S/C23H18ClN5O/c1-15-4-9-19(27-22(30)16-5-7-18(24)8-6-16)13-21(15)29-23-26-12-10-20(28-23)17-3-2-11-25-14-17/h2-14H,1H3,(H,27,30)(H,26,28,29) | PDB
Reactome pathway
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| CHEMBL
PC cid
PC sid
UniChem
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| Article
| n/a | n/a | 10 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of tyrosine kinase(PDGF-R) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Platelet-derived growth factor receptor alpha/beta
(Homo sapiens (Human)) | BDBM50175491
(4-Methyl-N-[4-methyl-3-(4-pyridin-3-yl-pyrimidin-2...)Show SMILES Cc1ccc(cc1)C(=O)Nc1ccc(C)c(Nc2nccc(n2)-c2cccnc2)c1 Show InChI InChI=1S/C24H21N5O/c1-16-5-8-18(9-6-16)23(30)27-20-10-7-17(2)22(14-20)29-24-26-13-11-21(28-24)19-4-3-12-25-15-19/h3-15H,1-2H3,(H,27,30)(H,26,28,29) | PDB
Reactome pathway
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| CHEMBL
PC cid
PC sid
UniChem
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| Article
| n/a | n/a | 10 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of tyrosine kinase(PDGF-R) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Platelet-derived growth factor receptor alpha/beta
(Homo sapiens (Human)) | BDBM50287091
(CHEMBL20252 | Naphthalene-2-carboxylic acid [4-met...)Show SMILES Cc1ccc(NC(=O)c2ccc3ccccc3c2)cc1Nc1nccc(n1)-c1cccnc1 Show InChI InChI=1S/C27H21N5O/c1-18-8-11-23(30-26(33)21-10-9-19-5-2-3-6-20(19)15-21)16-25(18)32-27-29-14-12-24(31-27)22-7-4-13-28-17-22/h2-17H,1H3,(H,30,33)(H,29,31,32) | PDB
Reactome pathway
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| CHEMBL
PC cid
PC sid
UniChem
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| Article
| n/a | n/a | 50 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of tyrosine kinase(PDGF-R) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Platelet-derived growth factor receptor alpha/beta
(Homo sapiens (Human)) | BDBM50240407
(CHEMBL20926 | N-(4-methyl-3-(4-(pyridin-3-yl)pyrim...)Show SMILES Cc1ccc(NC(=O)c2ccccc2)cc1Nc1nccc(n1)-c1cccnc1 Show InChI InChI=1S/C23H19N5O/c1-16-9-10-19(26-22(29)17-6-3-2-4-7-17)14-21(16)28-23-25-13-11-20(27-23)18-8-5-12-24-15-18/h2-15H,1H3,(H,26,29)(H,25,27,28) | PDB
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| Article
| n/a | n/a | 100 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of tyrosine kinase(PDGF-R) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Platelet-derived growth factor receptor alpha/beta
(Homo sapiens (Human)) | BDBM50287094
(CHEMBL278630 | N-[4-Chloro-3-(4-pyridin-3-yl-pyrim...)Show SMILES Clc1ccc(NC(=O)c2ccccc2)cc1Nc1nccc(n1)-c1cccnc1 Show InChI InChI=1S/C22H16ClN5O/c23-18-9-8-17(26-21(29)15-5-2-1-3-6-15)13-20(18)28-22-25-12-10-19(27-22)16-7-4-11-24-14-16/h1-14H,(H,26,29)(H,25,27,28) | PDB
Reactome pathway
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| CHEMBL
PC cid
PC sid
UniChem
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| Article
| n/a | n/a | 150 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of tyrosine kinase(PDGF-R) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Platelet-derived growth factor receptor alpha/beta
(Homo sapiens (Human)) | BDBM50287096
(2-Methoxy-N-[4-methyl-3-(4-pyridin-3-yl-pyrimidin-...)Show SMILES COc1ccccc1C(=O)Nc1ccc(C)c(Nc2nccc(n2)-c2cccnc2)c1 Show InChI InChI=1S/C24H21N5O2/c1-16-9-10-18(27-23(30)19-7-3-4-8-22(19)31-2)14-21(16)29-24-26-13-11-20(28-24)17-6-5-12-25-15-17/h3-15H,1-2H3,(H,27,30)(H,26,28,29) | PDB
Reactome pathway
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PC sid
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| Article
| n/a | n/a | 300 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of tyrosine kinase(PDGF-R) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Protein kinase C alpha type
(Homo sapiens (Human)) | BDBM50175493
(CHEMBL277931 | N-[3-(4-Pyridin-3-yl-pyrimidin-2-yl...)Show SMILES O=C(Nc1cccc(Nc2nccc(n2)-c2cccnc2)c1)c1ccccc1 Show InChI InChI=1S/C22H17N5O/c28-21(16-6-2-1-3-7-16)25-18-9-4-10-19(14-18)26-22-24-13-11-20(27-22)17-8-5-12-23-15-17/h1-15H,(H,25,28)(H,24,26,27) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
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| CHEMBL
PC cid
PC sid
UniChem
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| Article
| n/a | n/a | 1.20E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of serine/threonine kinase(PKC-alpha) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Platelet-derived growth factor receptor alpha/beta
(Homo sapiens (Human)) | BDBM50287092
(CHEMBL277430 | N-Benzoyl-N-[4-methyl-3-(4-pyridin-...)Show SMILES Cc1ccc(cc1Nc1nccc(n1)-c1cccnc1)N(C(=O)c1ccccc1)C(=O)c1ccccc1 Show InChI InChI=1S/C30H23N5O2/c1-21-14-15-25(19-27(21)34-30-32-18-16-26(33-30)24-13-8-17-31-20-24)35(28(36)22-9-4-2-5-10-22)29(37)23-11-6-3-7-12-23/h2-20H,1H3,(H,32,33,34) | PDB
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PC cid
PC sid
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| Article
| n/a | n/a | 2.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of tyrosine kinase(PDGF-R) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Platelet-derived growth factor receptor alpha/beta
(Homo sapiens (Human)) | BDBM50175493
(CHEMBL277931 | N-[3-(4-Pyridin-3-yl-pyrimidin-2-yl...)Show SMILES O=C(Nc1cccc(Nc2nccc(n2)-c2cccnc2)c1)c1ccccc1 Show InChI InChI=1S/C22H17N5O/c28-21(16-6-2-1-3-7-16)25-18-9-4-10-19(14-18)26-22-24-13-11-20(27-22)17-8-5-12-23-15-17/h1-15H,(H,25,28)(H,24,26,27) | PDB
Reactome pathway
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| CHEMBL
PC cid
PC sid
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| Article
| n/a | n/a | 5.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of tyrosine kinase(PDGF-R) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Platelet-derived growth factor receptor alpha/beta
(Homo sapiens (Human)) | BDBM50287087
(CHEMBL21078 | N-[4-Methyl-3-(4-thiophen-2-yl-pyrim...)Show SMILES Cc1ccc(NC(=O)c2ccccc2)cc1Nc1nccc(n1)-c1cccs1 Show InChI InChI=1S/C22H18N4OS/c1-15-9-10-17(24-21(27)16-6-3-2-4-7-16)14-19(15)26-22-23-12-11-18(25-22)20-8-5-13-28-20/h2-14H,1H3,(H,24,27)(H,23,25,26) | PDB
Reactome pathway
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PC cid
PC sid
UniChem
| Article
| n/a | n/a | >1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of tyrosine kinase(PDGF-R) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Platelet-derived growth factor receptor alpha/beta
(Homo sapiens (Human)) | BDBM50287088
(CHEMBL21086 | N-[4-Methoxy-3-(4-pyridin-3-yl-pyrim...)Show SMILES COc1ccc(NC(=O)c2ccccc2)cc1Nc1nccc(n1)-c1cccnc1 Show InChI InChI=1S/C23H19N5O2/c1-30-21-10-9-18(26-22(29)16-6-3-2-4-7-16)14-20(21)28-23-25-13-11-19(27-23)17-8-5-12-24-15-17/h2-15H,1H3,(H,26,29)(H,25,27,28) | PDB
Reactome pathway
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| Article
| n/a | n/a | >1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of tyrosine kinase(PDGF-R) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Protein kinase C alpha type
(Homo sapiens (Human)) | BDBM50287088
(CHEMBL21086 | N-[4-Methoxy-3-(4-pyridin-3-yl-pyrim...)Show SMILES COc1ccc(NC(=O)c2ccccc2)cc1Nc1nccc(n1)-c1cccnc1 Show InChI InChI=1S/C23H19N5O2/c1-30-21-10-9-18(26-22(29)16-6-3-2-4-7-16)14-20(21)28-23-25-13-11-19(27-23)17-8-5-12-24-15-17/h2-15H,1H3,(H,26,29)(H,25,27,28) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
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| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
| n/a | n/a | 1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of serine/threonine kinase(PKC-alpha) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Platelet-derived growth factor receptor alpha/beta
(Homo sapiens (Human)) | BDBM50287097
(4-Methyl-N*3*-(4-pyridin-3-yl-pyrimidin-2-yl)-benz...)Show InChI InChI=1S/C16H15N5/c1-11-4-5-13(17)9-15(11)21-16-19-8-6-14(20-16)12-3-2-7-18-10-12/h2-10H,17H2,1H3,(H,19,20,21) | PDB
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| Article
| n/a | n/a | >1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of tyrosine kinase(PDGF-R) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Platelet-derived growth factor receptor alpha/beta
(Homo sapiens (Human)) | BDBM50287098
(CHEMBL21079 | N-{4-Methyl-3-[4-(1-oxy-pyridin-3-yl...)Show SMILES Cc1ccc(NC(=O)c2ccccc2)cc1Nc1nccc(n1)-c1ccc[n+]([O-])c1 Show InChI InChI=1S/C23H19N5O2/c1-16-9-10-19(25-22(29)17-6-3-2-4-7-17)14-21(16)27-23-24-12-11-20(26-23)18-8-5-13-28(30)15-18/h2-15H,1H3,(H,25,29)(H,24,26,27) | PDB
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| n/a | n/a | >1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of tyrosine kinase(PDGF-R) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Platelet-derived growth factor receptor alpha/beta
(Homo sapiens (Human)) | BDBM50287095
(4,N*1*-Dimethyl-N*3*-(4-pyridin-3-yl-pyrimidin-2-y...)Show InChI InChI=1S/C17H17N5/c1-12-5-6-14(18-2)10-16(12)22-17-20-9-7-15(21-17)13-4-3-8-19-11-13/h3-11,18H,1-2H3,(H,20,21,22) | PDB
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| n/a | n/a | >1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of tyrosine kinase(PDGF-R) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Proto-oncogene tyrosine-protein kinase Src
(Homo sapiens (Human)) | BDBM50175493
(CHEMBL277931 | N-[3-(4-Pyridin-3-yl-pyrimidin-2-yl...)Show SMILES O=C(Nc1cccc(Nc2nccc(n2)-c2cccnc2)c1)c1ccccc1 Show InChI InChI=1S/C22H17N5O/c28-21(16-6-2-1-3-7-16)25-18-9-4-10-19(14-18)26-22-24-13-11-20(27-22)17-8-5-12-23-15-17/h1-15H,(H,25,28)(H,24,26,27) | PDB
MMDB
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PC cid
PC sid
UniChem
Patents
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| Article
| n/a | n/a | 1.57E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of tyrosine kinase(c-Src) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Protein kinase C delta type
(Homo sapiens (Human)) | BDBM50175493
(CHEMBL277931 | N-[3-(4-Pyridin-3-yl-pyrimidin-2-yl...)Show SMILES O=C(Nc1cccc(Nc2nccc(n2)-c2cccnc2)c1)c1ccccc1 Show InChI InChI=1S/C22H17N5O/c28-21(16-6-2-1-3-7-16)25-18-9-4-10-19(14-18)26-22-24-13-11-20(27-22)17-8-5-12-23-15-17/h1-15H,(H,25,28)(H,24,26,27) | PDB
MMDB
NCI pathway
Reactome pathway
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| CHEMBL
PC cid
PC sid
UniChem
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| Article
| n/a | n/a | 2.30E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of serine/threonine kinase(PKC-delta) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Epidermal growth factor receptor
(Homo sapiens (Human)) | BDBM50287089
(CHEMBL278287 | N-Methyl-N-[4-methyl-3-(4-pyridin-3...)Show SMILES CN(C(=O)c1ccccc1)c1ccc(C)c(Nc2nccc(n2)-c2cccnc2)c1 Show InChI InChI=1S/C24H21N5O/c1-17-10-11-20(29(2)23(30)18-7-4-3-5-8-18)15-22(17)28-24-26-14-12-21(27-24)19-9-6-13-25-16-19/h3-16H,1-2H3,(H,26,27,28) | PDB
MMDB
KEGG
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| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
| n/a | n/a | 4.90E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of tyrosine kinase Epidermal growth factor receptor |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Epidermal growth factor receptor
(Homo sapiens (Human)) | BDBM50175493
(CHEMBL277931 | N-[3-(4-Pyridin-3-yl-pyrimidin-2-yl...)Show SMILES O=C(Nc1cccc(Nc2nccc(n2)-c2cccnc2)c1)c1ccccc1 Show InChI InChI=1S/C22H17N5O/c28-21(16-6-2-1-3-7-16)25-18-9-4-10-19(14-18)26-22-24-13-11-20(27-22)17-8-5-12-23-15-17/h1-15H,(H,25,28)(H,24,26,27) | PDB
MMDB
KEGG
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| CHEMBL
PC cid
PC sid
UniChem
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| Article
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of tyrosine kinase Epidermal growth factor receptor |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Platelet-derived growth factor receptor alpha/beta
(Homo sapiens (Human)) | BDBM50240406
(CHEMBL423288 | N-(4-methyl-3-(4-(pyridin-3-yl)pyri...)Show InChI InChI=1S/C18H17N5O/c1-12-5-6-15(21-13(2)24)10-17(12)23-18-20-9-7-16(22-18)14-4-3-8-19-11-14/h3-11H,1-2H3,(H,21,24)(H,20,22,23) | PDB
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| n/a | n/a | 5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of tyrosine kinase(PDGF-R) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Protein kinase C alpha type
(Homo sapiens (Human)) | BDBM50287095
(4,N*1*-Dimethyl-N*3*-(4-pyridin-3-yl-pyrimidin-2-y...)Show InChI InChI=1S/C17H17N5/c1-12-5-6-14(18-2)10-16(12)22-17-20-9-7-15(21-17)13-4-3-8-19-11-13/h3-11,18H,1-2H3,(H,20,21,22) | PDB
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| n/a | n/a | 7.10E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of serine/threonine kinase(PKC-alpha) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Protein kinase C alpha type
(Homo sapiens (Human)) | BDBM50240407
(CHEMBL20926 | N-(4-methyl-3-(4-(pyridin-3-yl)pyrim...)Show SMILES Cc1ccc(NC(=O)c2ccccc2)cc1Nc1nccc(n1)-c1cccnc1 Show InChI InChI=1S/C23H19N5O/c1-16-9-10-19(26-22(29)17-6-3-2-4-7-17)14-21(16)28-23-25-13-11-20(27-23)18-8-5-12-24-15-18/h2-15H,1H3,(H,26,29)(H,25,27,28) | PDB
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| n/a | n/a | 7.20E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of serine/threonine kinase(PKC-alpha) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Epidermal growth factor receptor
(Homo sapiens (Human)) | BDBM50287092
(CHEMBL277430 | N-Benzoyl-N-[4-methyl-3-(4-pyridin-...)Show SMILES Cc1ccc(cc1Nc1nccc(n1)-c1cccnc1)N(C(=O)c1ccccc1)C(=O)c1ccccc1 Show InChI InChI=1S/C30H23N5O2/c1-21-14-15-25(19-27(21)34-30-32-18-16-26(33-30)24-13-8-17-31-20-24)35(28(36)22-9-4-2-5-10-22)29(37)23-11-6-3-7-12-23/h2-20H,1H3,(H,32,33,34) | PDB
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| n/a | n/a | 7.50E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of tyrosine kinase Epidermal growth factor receptor |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Protein kinase C alpha type
(Homo sapiens (Human)) | BDBM50287089
(CHEMBL278287 | N-Methyl-N-[4-methyl-3-(4-pyridin-3...)Show SMILES CN(C(=O)c1ccccc1)c1ccc(C)c(Nc2nccc(n2)-c2cccnc2)c1 Show InChI InChI=1S/C24H21N5O/c1-17-10-11-20(29(2)23(30)18-7-4-3-5-8-18)15-22(17)28-24-26-14-12-21(27-24)19-9-6-13-25-16-19/h3-16H,1-2H3,(H,26,27,28) | PDB
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| n/a | n/a | 8.50E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of serine/threonine kinase(PKC-alpha) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Protein kinase C alpha type
(Homo sapiens (Human)) | BDBM50287096
(2-Methoxy-N-[4-methyl-3-(4-pyridin-3-yl-pyrimidin-...)Show SMILES COc1ccccc1C(=O)Nc1ccc(C)c(Nc2nccc(n2)-c2cccnc2)c1 Show InChI InChI=1S/C24H21N5O2/c1-16-9-10-18(27-23(30)19-7-3-4-8-22(19)31-2)14-21(16)29-24-26-13-11-20(28-24)17-6-5-12-25-15-17/h3-15H,1-2H3,(H,27,30)(H,26,28,29) | PDB
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| n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of serine/threonine kinase(PKC-alpha) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Protein kinase C delta type
(Homo sapiens (Human)) | BDBM50287094
(CHEMBL278630 | N-[4-Chloro-3-(4-pyridin-3-yl-pyrim...)Show SMILES Clc1ccc(NC(=O)c2ccccc2)cc1Nc1nccc(n1)-c1cccnc1 Show InChI InChI=1S/C22H16ClN5O/c23-18-9-8-17(26-21(29)15-5-2-1-3-6-15)13-20(18)28-22-25-12-10-19(27-22)16-7-4-11-24-14-16/h1-14H,(H,26,29)(H,25,27,28) | PDB
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| n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of serine/threonine kinase(PKC-delta) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Proto-oncogene tyrosine-protein kinase Src
(Homo sapiens (Human)) | BDBM50175491
(4-Methyl-N-[4-methyl-3-(4-pyridin-3-yl-pyrimidin-2...)Show SMILES Cc1ccc(cc1)C(=O)Nc1ccc(C)c(Nc2nccc(n2)-c2cccnc2)c1 Show InChI InChI=1S/C24H21N5O/c1-16-5-8-18(9-6-16)23(30)27-20-10-7-17(2)22(14-20)29-24-26-13-11-21(28-24)19-4-3-12-25-15-19/h3-15H,1-2H3,(H,27,30)(H,26,28,29) | PDB
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| n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of tyrosine kinase(c-Src) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
cAMP-dependent protein kinase catalytic subunit alpha/beta/gamma
(Homo sapiens (Human)) | BDBM50287091
(CHEMBL20252 | Naphthalene-2-carboxylic acid [4-met...)Show SMILES Cc1ccc(NC(=O)c2ccc3ccccc3c2)cc1Nc1nccc(n1)-c1cccnc1 Show InChI InChI=1S/C27H21N5O/c1-18-8-11-23(30-26(33)21-10-9-19-5-2-3-6-20(19)15-21)16-25(18)32-27-29-14-12-24(31-27)22-7-4-13-28-17-22/h2-17H,1H3,(H,30,33)(H,29,31,32) | PDB
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| n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of tyrosine kinase(PDGF-R) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Proto-oncogene tyrosine-protein kinase Src
(Homo sapiens (Human)) | BDBM50240407
(CHEMBL20926 | N-(4-methyl-3-(4-(pyridin-3-yl)pyrim...)Show SMILES Cc1ccc(NC(=O)c2ccccc2)cc1Nc1nccc(n1)-c1cccnc1 Show InChI InChI=1S/C23H19N5O/c1-16-9-10-19(26-22(29)17-6-3-2-4-7-17)14-21(16)28-23-25-13-11-20(27-23)18-8-5-12-24-15-18/h2-15H,1H3,(H,26,29)(H,25,27,28) | PDB
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| n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of tyrosine kinase(c-Src) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Protein kinase C alpha type
(Homo sapiens (Human)) | BDBM50287091
(CHEMBL20252 | Naphthalene-2-carboxylic acid [4-met...)Show SMILES Cc1ccc(NC(=O)c2ccc3ccccc3c2)cc1Nc1nccc(n1)-c1cccnc1 Show InChI InChI=1S/C27H21N5O/c1-18-8-11-23(30-26(33)21-10-9-19-5-2-3-6-20(19)15-21)16-25(18)32-27-29-14-12-24(31-27)22-7-4-13-28-17-22/h2-17H,1H3,(H,30,33)(H,29,31,32) | PDB
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| n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of serine/threonine kinase(PKC-alpha) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Protein kinase C alpha type
(Homo sapiens (Human)) | BDBM50287090
(4-Chloro-N-[4-methyl-3-(4-pyridin-3-yl-pyrimidin-2...)Show SMILES Cc1ccc(NC(=O)c2ccc(Cl)cc2)cc1Nc1nccc(n1)-c1cccnc1 Show InChI InChI=1S/C23H18ClN5O/c1-15-4-9-19(27-22(30)16-5-7-18(24)8-6-16)13-21(15)29-23-26-12-10-20(28-23)17-3-2-11-25-14-17/h2-14H,1H3,(H,27,30)(H,26,28,29) | PDB
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| n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of serine/threonine kinase(PKC-alpha) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Epidermal growth factor receptor
(Homo sapiens (Human)) | BDBM50287088
(CHEMBL21086 | N-[4-Methoxy-3-(4-pyridin-3-yl-pyrim...)Show SMILES COc1ccc(NC(=O)c2ccccc2)cc1Nc1nccc(n1)-c1cccnc1 Show InChI InChI=1S/C23H19N5O2/c1-30-21-10-9-18(26-22(29)16-6-3-2-4-7-16)14-20(21)28-23-25-13-11-19(27-23)17-8-5-12-24-15-17/h2-15H,1H3,(H,26,29)(H,25,27,28) | PDB
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| n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of tyrosine kinase Epidermal growth factor receptor |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Epidermal growth factor receptor
(Homo sapiens (Human)) | BDBM50240406
(CHEMBL423288 | N-(4-methyl-3-(4-(pyridin-3-yl)pyri...)Show InChI InChI=1S/C18H17N5O/c1-12-5-6-15(21-13(2)24)10-17(12)23-18-20-9-7-16(22-18)14-4-3-8-19-11-14/h3-11H,1-2H3,(H,21,24)(H,20,22,23) | PDB
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| n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of tyrosine kinase Epidermal growth factor receptor |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Epidermal growth factor receptor
(Homo sapiens (Human)) | BDBM50287093
((2-Methyl-5-nitro-phenyl)-(4-pyridin-3-yl-pyrimidi...)Show SMILES Cc1ccc(cc1Nc1nccc(n1)-c1cccnc1)[N+]([O-])=O Show InChI InChI=1S/C16H13N5O2/c1-11-4-5-13(21(22)23)9-15(11)20-16-18-8-6-14(19-16)12-3-2-7-17-10-12/h2-10H,1H3,(H,18,19,20) | PDB
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| n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of tyrosine kinase Epidermal growth factor receptor |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Epidermal growth factor receptor
(Homo sapiens (Human)) | BDBM50287094
(CHEMBL278630 | N-[4-Chloro-3-(4-pyridin-3-yl-pyrim...)Show SMILES Clc1ccc(NC(=O)c2ccccc2)cc1Nc1nccc(n1)-c1cccnc1 Show InChI InChI=1S/C22H16ClN5O/c23-18-9-8-17(26-21(29)15-5-2-1-3-6-15)13-20(18)28-22-25-12-10-19(27-22)16-7-4-11-24-14-16/h1-14H,(H,26,29)(H,25,27,28) | PDB
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| n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of tyrosine kinase Epidermal growth factor receptor |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
cAMP-dependent protein kinase catalytic subunit alpha/beta/gamma
(Homo sapiens (Human)) | BDBM50287090
(4-Chloro-N-[4-methyl-3-(4-pyridin-3-yl-pyrimidin-2...)Show SMILES Cc1ccc(NC(=O)c2ccc(Cl)cc2)cc1Nc1nccc(n1)-c1cccnc1 Show InChI InChI=1S/C23H18ClN5O/c1-15-4-9-19(27-22(30)16-5-7-18(24)8-6-16)13-21(15)29-23-26-12-10-20(28-23)17-3-2-11-25-14-17/h2-14H,1H3,(H,27,30)(H,26,28,29) | PDB
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| n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of serine/threonine kinase(PKA) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Protein kinase C delta type
(Homo sapiens (Human)) | BDBM50287087
(CHEMBL21078 | N-[4-Methyl-3-(4-thiophen-2-yl-pyrim...)Show SMILES Cc1ccc(NC(=O)c2ccccc2)cc1Nc1nccc(n1)-c1cccs1 Show InChI InChI=1S/C22H18N4OS/c1-15-9-10-17(24-21(27)16-6-3-2-4-7-16)14-19(15)26-22-23-12-11-18(25-22)20-8-5-13-28-20/h2-14H,1H3,(H,24,27)(H,23,25,26) | PDB
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| n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of serine/threonine kinase(PKC-delta) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Epidermal growth factor receptor
(Homo sapiens (Human)) | BDBM50287095
(4,N*1*-Dimethyl-N*3*-(4-pyridin-3-yl-pyrimidin-2-y...)Show InChI InChI=1S/C17H17N5/c1-12-5-6-14(18-2)10-16(12)22-17-20-9-7-15(21-17)13-4-3-8-19-11-13/h3-11,18H,1-2H3,(H,20,21,22) | PDB
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| n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of tyrosine kinase Epidermal growth factor receptor |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Platelet-derived growth factor receptor alpha/beta
(Homo sapiens (Human)) | BDBM50287093
((2-Methyl-5-nitro-phenyl)-(4-pyridin-3-yl-pyrimidi...)Show SMILES Cc1ccc(cc1Nc1nccc(n1)-c1cccnc1)[N+]([O-])=O Show InChI InChI=1S/C16H13N5O2/c1-11-4-5-13(21(22)23)9-15(11)20-16-18-8-6-14(19-16)12-3-2-7-17-10-12/h2-10H,1H3,(H,18,19,20) | PDB
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| n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of tyrosine kinase(PDGF-R) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Proto-oncogene tyrosine-protein kinase Src
(Homo sapiens (Human)) | BDBM50287087
(CHEMBL21078 | N-[4-Methyl-3-(4-thiophen-2-yl-pyrim...)Show SMILES Cc1ccc(NC(=O)c2ccccc2)cc1Nc1nccc(n1)-c1cccs1 Show InChI InChI=1S/C22H18N4OS/c1-15-9-10-17(24-21(27)16-6-3-2-4-7-16)14-19(15)26-22-23-12-11-18(25-22)20-8-5-13-28-20/h2-14H,1H3,(H,24,27)(H,23,25,26) | PDB
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| n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of tyrosine kinase(c-Src) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Proto-oncogene tyrosine-protein kinase Src
(Homo sapiens (Human)) | BDBM50287096
(2-Methoxy-N-[4-methyl-3-(4-pyridin-3-yl-pyrimidin-...)Show SMILES COc1ccccc1C(=O)Nc1ccc(C)c(Nc2nccc(n2)-c2cccnc2)c1 Show InChI InChI=1S/C24H21N5O2/c1-16-9-10-18(27-23(30)19-7-3-4-8-22(19)31-2)14-21(16)29-24-26-13-11-20(28-24)17-6-5-12-25-15-17/h3-15H,1-2H3,(H,27,30)(H,26,28,29) | PDB
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| n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of tyrosine kinase(c-Src) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Protein kinase C delta type
(Homo sapiens (Human)) | BDBM50287088
(CHEMBL21086 | N-[4-Methoxy-3-(4-pyridin-3-yl-pyrim...)Show SMILES COc1ccc(NC(=O)c2ccccc2)cc1Nc1nccc(n1)-c1cccnc1 Show InChI InChI=1S/C23H19N5O2/c1-30-21-10-9-18(26-22(29)16-6-3-2-4-7-16)14-20(21)28-23-25-13-11-19(27-23)17-8-5-12-24-15-17/h2-15H,1H3,(H,26,29)(H,25,27,28) | PDB
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| n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of serine/threonine kinase(PKC-delta) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Protein kinase C alpha type
(Homo sapiens (Human)) | BDBM50175491
(4-Methyl-N-[4-methyl-3-(4-pyridin-3-yl-pyrimidin-2...)Show SMILES Cc1ccc(cc1)C(=O)Nc1ccc(C)c(Nc2nccc(n2)-c2cccnc2)c1 Show InChI InChI=1S/C24H21N5O/c1-16-5-8-18(9-6-16)23(30)27-20-10-7-17(2)22(14-20)29-24-26-13-11-21(28-24)19-4-3-12-25-15-19/h3-15H,1-2H3,(H,27,30)(H,26,28,29) | PDB
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| n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of serine/threonine kinase(PKC-alpha) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Epidermal growth factor receptor
(Homo sapiens (Human)) | BDBM50175491
(4-Methyl-N-[4-methyl-3-(4-pyridin-3-yl-pyrimidin-2...)Show SMILES Cc1ccc(cc1)C(=O)Nc1ccc(C)c(Nc2nccc(n2)-c2cccnc2)c1 Show InChI InChI=1S/C24H21N5O/c1-16-5-8-18(9-6-16)23(30)27-20-10-7-17(2)22(14-20)29-24-26-13-11-21(28-24)19-4-3-12-25-15-19/h3-15H,1-2H3,(H,27,30)(H,26,28,29) | PDB
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| n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of tyrosine kinase Epidermal growth factor receptor |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Epidermal growth factor receptor
(Homo sapiens (Human)) | BDBM50287096
(2-Methoxy-N-[4-methyl-3-(4-pyridin-3-yl-pyrimidin-...)Show SMILES COc1ccccc1C(=O)Nc1ccc(C)c(Nc2nccc(n2)-c2cccnc2)c1 Show InChI InChI=1S/C24H21N5O2/c1-16-9-10-18(27-23(30)19-7-3-4-8-22(19)31-2)14-21(16)29-24-26-13-11-20(28-24)17-6-5-12-25-15-17/h3-15H,1-2H3,(H,27,30)(H,26,28,29) | PDB
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| n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of tyrosine kinase Epidermal growth factor receptor |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Proto-oncogene tyrosine-protein kinase Src
(Homo sapiens (Human)) | BDBM50240406
(CHEMBL423288 | N-(4-methyl-3-(4-(pyridin-3-yl)pyri...)Show InChI InChI=1S/C18H17N5O/c1-12-5-6-15(21-13(2)24)10-17(12)23-18-20-9-7-16(22-18)14-4-3-8-19-11-14/h3-11H,1-2H3,(H,21,24)(H,20,22,23) | PDB
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| n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of tyrosine kinase(c-Src) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Protein kinase C delta type
(Homo sapiens (Human)) | BDBM50287089
(CHEMBL278287 | N-Methyl-N-[4-methyl-3-(4-pyridin-3...)Show SMILES CN(C(=O)c1ccccc1)c1ccc(C)c(Nc2nccc(n2)-c2cccnc2)c1 Show InChI InChI=1S/C24H21N5O/c1-17-10-11-20(29(2)23(30)18-7-4-3-5-8-18)15-22(17)28-24-26-14-12-21(27-24)19-9-6-13-25-16-19/h3-16H,1-2H3,(H,26,27,28) | PDB
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| n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of serine/threonine kinase(PKC-delta) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Protein kinase C delta type
(Homo sapiens (Human)) | BDBM50287098
(CHEMBL21079 | N-{4-Methyl-3-[4-(1-oxy-pyridin-3-yl...)Show SMILES Cc1ccc(NC(=O)c2ccccc2)cc1Nc1nccc(n1)-c1ccc[n+]([O-])c1 Show InChI InChI=1S/C23H19N5O2/c1-16-9-10-19(25-22(29)17-6-3-2-4-7-17)14-21(16)27-23-24-12-11-20(26-23)18-8-5-13-28(30)15-18/h2-15H,1H3,(H,25,29)(H,24,26,27) | PDB
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| n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of serine/threonine kinase(PKC-delta) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Protein kinase C alpha type
(Homo sapiens (Human)) | BDBM50287092
(CHEMBL277430 | N-Benzoyl-N-[4-methyl-3-(4-pyridin-...)Show SMILES Cc1ccc(cc1Nc1nccc(n1)-c1cccnc1)N(C(=O)c1ccccc1)C(=O)c1ccccc1 Show InChI InChI=1S/C30H23N5O2/c1-21-14-15-25(19-27(21)34-30-32-18-16-26(33-30)24-13-8-17-31-20-24)35(28(36)22-9-4-2-5-10-22)29(37)23-11-6-3-7-12-23/h2-20H,1H3,(H,32,33,34) | PDB
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| n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of serine/threonine kinase(PKC-alpha) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Proto-oncogene tyrosine-protein kinase Src
(Homo sapiens (Human)) | BDBM50287091
(CHEMBL20252 | Naphthalene-2-carboxylic acid [4-met...)Show SMILES Cc1ccc(NC(=O)c2ccc3ccccc3c2)cc1Nc1nccc(n1)-c1cccnc1 Show InChI InChI=1S/C27H21N5O/c1-18-8-11-23(30-26(33)21-10-9-19-5-2-3-6-20(19)15-21)16-25(18)32-27-29-14-12-24(31-27)22-7-4-13-28-17-22/h2-17H,1H3,(H,30,33)(H,29,31,32) | PDB
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| n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of tyrosine kinase(c-Src) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Proto-oncogene tyrosine-protein kinase Src
(Homo sapiens (Human)) | BDBM50287093
((2-Methyl-5-nitro-phenyl)-(4-pyridin-3-yl-pyrimidi...)Show SMILES Cc1ccc(cc1Nc1nccc(n1)-c1cccnc1)[N+]([O-])=O Show InChI InChI=1S/C16H13N5O2/c1-11-4-5-13(21(22)23)9-15(11)20-16-18-8-6-14(19-16)12-3-2-7-17-10-12/h2-10H,1H3,(H,18,19,20) | PDB
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| n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of tyrosine kinase(c-Src) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Platelet-derived growth factor receptor alpha/beta
(Homo sapiens (Human)) | BDBM50287089
(CHEMBL278287 | N-Methyl-N-[4-methyl-3-(4-pyridin-3...)Show SMILES CN(C(=O)c1ccccc1)c1ccc(C)c(Nc2nccc(n2)-c2cccnc2)c1 Show InChI InChI=1S/C24H21N5O/c1-17-10-11-20(29(2)23(30)18-7-4-3-5-8-18)15-22(17)28-24-26-14-12-21(27-24)19-9-6-13-25-16-19/h3-16H,1-2H3,(H,26,27,28) | PDB
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| n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of tyrosine kinase(PDGF-R) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
cAMP-dependent protein kinase catalytic subunit alpha/beta/gamma
(Homo sapiens (Human)) | BDBM50175491
(4-Methyl-N-[4-methyl-3-(4-pyridin-3-yl-pyrimidin-2...)Show SMILES Cc1ccc(cc1)C(=O)Nc1ccc(C)c(Nc2nccc(n2)-c2cccnc2)c1 Show InChI InChI=1S/C24H21N5O/c1-16-5-8-18(9-6-16)23(30)27-20-10-7-17(2)22(14-20)29-24-26-13-11-21(28-24)19-4-3-12-25-15-19/h3-15H,1-2H3,(H,27,30)(H,26,28,29) | PDB
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| n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of serine/threonine kinase(PKA) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Protein kinase C alpha type
(Homo sapiens (Human)) | BDBM50287094
(CHEMBL278630 | N-[4-Chloro-3-(4-pyridin-3-yl-pyrim...)Show SMILES Clc1ccc(NC(=O)c2ccccc2)cc1Nc1nccc(n1)-c1cccnc1 Show InChI InChI=1S/C22H16ClN5O/c23-18-9-8-17(26-21(29)15-5-2-1-3-6-15)13-20(18)28-22-25-12-10-19(27-22)16-7-4-11-24-14-16/h1-14H,(H,26,29)(H,25,27,28) | PDB
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| n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of serine/threonine kinase(PKC-alpha) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Protein kinase C alpha type
(Homo sapiens (Human)) | BDBM50287097
(4-Methyl-N*3*-(4-pyridin-3-yl-pyrimidin-2-yl)-benz...)Show InChI InChI=1S/C16H15N5/c1-11-4-5-13(17)9-15(11)21-16-19-8-6-14(20-16)12-3-2-7-18-10-12/h2-10H,17H2,1H3,(H,19,20,21) | PDB
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| n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of serine/threonine kinase(PKC-alpha) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Epidermal growth factor receptor
(Homo sapiens (Human)) | BDBM50287090
(4-Chloro-N-[4-methyl-3-(4-pyridin-3-yl-pyrimidin-2...)Show SMILES Cc1ccc(NC(=O)c2ccc(Cl)cc2)cc1Nc1nccc(n1)-c1cccnc1 Show InChI InChI=1S/C23H18ClN5O/c1-15-4-9-19(27-22(30)16-5-7-18(24)8-6-16)13-21(15)29-23-26-12-10-20(28-23)17-3-2-11-25-14-17/h2-14H,1H3,(H,27,30)(H,26,28,29) | PDB
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TBA
Curated by ChEMBL
| Assay Description
Inhibition of tyrosine kinase Epidermal growth factor receptor |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Epidermal growth factor receptor
(Homo sapiens (Human)) | BDBM50287091
(CHEMBL20252 | Naphthalene-2-carboxylic acid [4-met...)Show SMILES Cc1ccc(NC(=O)c2ccc3ccccc3c2)cc1Nc1nccc(n1)-c1cccnc1 Show InChI InChI=1S/C27H21N5O/c1-18-8-11-23(30-26(33)21-10-9-19-5-2-3-6-20(19)15-21)16-25(18)32-27-29-14-12-24(31-27)22-7-4-13-28-17-22/h2-17H,1H3,(H,30,33)(H,29,31,32) | PDB
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TBA
Curated by ChEMBL
| Assay Description
Inhibition of tyrosine kinase Epidermal growth factor receptor |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Epidermal growth factor receptor
(Homo sapiens (Human)) | BDBM50287087
(CHEMBL21078 | N-[4-Methyl-3-(4-thiophen-2-yl-pyrim...)Show SMILES Cc1ccc(NC(=O)c2ccccc2)cc1Nc1nccc(n1)-c1cccs1 Show InChI InChI=1S/C22H18N4OS/c1-15-9-10-17(24-21(27)16-6-3-2-4-7-16)14-19(15)26-22-23-12-11-18(25-22)20-8-5-13-28-20/h2-14H,1H3,(H,24,27)(H,23,25,26) | PDB
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TBA
Curated by ChEMBL
| Assay Description
Inhibition of tyrosine kinase Epidermal growth factor receptor |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Proto-oncogene tyrosine-protein kinase Src
(Homo sapiens (Human)) | BDBM50287097
(4-Methyl-N*3*-(4-pyridin-3-yl-pyrimidin-2-yl)-benz...)Show InChI InChI=1S/C16H15N5/c1-11-4-5-13(17)9-15(11)21-16-19-8-6-14(20-16)12-3-2-7-18-10-12/h2-10H,17H2,1H3,(H,19,20,21) | PDB
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TBA
Curated by ChEMBL
| Assay Description
Inhibition of tyrosine kinase(c-Src) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Protein kinase C alpha type
(Homo sapiens (Human)) | BDBM50240406
(CHEMBL423288 | N-(4-methyl-3-(4-(pyridin-3-yl)pyri...)Show InChI InChI=1S/C18H17N5O/c1-12-5-6-15(21-13(2)24)10-17(12)23-18-20-9-7-16(22-18)14-4-3-8-19-11-14/h3-11H,1-2H3,(H,21,24)(H,20,22,23) | PDB
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TBA
Curated by ChEMBL
| Assay Description
Inhibition of serine/threonine kinase(PKC-alpha) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Protein kinase C alpha type
(Homo sapiens (Human)) | BDBM50287098
(CHEMBL21079 | N-{4-Methyl-3-[4-(1-oxy-pyridin-3-yl...)Show SMILES Cc1ccc(NC(=O)c2ccccc2)cc1Nc1nccc(n1)-c1ccc[n+]([O-])c1 Show InChI InChI=1S/C23H19N5O2/c1-16-9-10-19(25-22(29)17-6-3-2-4-7-17)14-21(16)27-23-24-12-11-20(26-23)18-8-5-13-28(30)15-18/h2-15H,1H3,(H,25,29)(H,24,26,27) | PDB
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TBA
Curated by ChEMBL
| Assay Description
Inhibition of serine/threonine kinase(PKC-alpha) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Epidermal growth factor receptor
(Homo sapiens (Human)) | BDBM50287097
(4-Methyl-N*3*-(4-pyridin-3-yl-pyrimidin-2-yl)-benz...)Show InChI InChI=1S/C16H15N5/c1-11-4-5-13(17)9-15(11)21-16-19-8-6-14(20-16)12-3-2-7-18-10-12/h2-10H,17H2,1H3,(H,19,20,21) | PDB
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TBA
Curated by ChEMBL
| Assay Description
Inhibition of tyrosine kinase Epidermal growth factor receptor |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Protein kinase C delta type
(Homo sapiens (Human)) | BDBM50287095
(4,N*1*-Dimethyl-N*3*-(4-pyridin-3-yl-pyrimidin-2-y...)Show InChI InChI=1S/C17H17N5/c1-12-5-6-14(18-2)10-16(12)22-17-20-9-7-15(21-17)13-4-3-8-19-11-13/h3-11,18H,1-2H3,(H,20,21,22) | PDB
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Similars
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| n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of serine/threonine kinase(PKC-delta) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Proto-oncogene tyrosine-protein kinase Src
(Homo sapiens (Human)) | BDBM50287090
(4-Chloro-N-[4-methyl-3-(4-pyridin-3-yl-pyrimidin-2...)Show SMILES Cc1ccc(NC(=O)c2ccc(Cl)cc2)cc1Nc1nccc(n1)-c1cccnc1 Show InChI InChI=1S/C23H18ClN5O/c1-15-4-9-19(27-22(30)16-5-7-18(24)8-6-16)13-21(15)29-23-26-12-10-20(28-23)17-3-2-11-25-14-17/h2-14H,1H3,(H,27,30)(H,26,28,29) | PDB
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TBA
Curated by ChEMBL
| Assay Description
Inhibition of tyrosine kinase(c-Src) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Protein kinase C delta type
(Homo sapiens (Human)) | BDBM50287092
(CHEMBL277430 | N-Benzoyl-N-[4-methyl-3-(4-pyridin-...)Show SMILES Cc1ccc(cc1Nc1nccc(n1)-c1cccnc1)N(C(=O)c1ccccc1)C(=O)c1ccccc1 Show InChI InChI=1S/C30H23N5O2/c1-21-14-15-25(19-27(21)34-30-32-18-16-26(33-30)24-13-8-17-31-20-24)35(28(36)22-9-4-2-5-10-22)29(37)23-11-6-3-7-12-23/h2-20H,1H3,(H,32,33,34) | PDB
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TBA
Curated by ChEMBL
| Assay Description
Inhibition of serine/threonine kinase(PKC-delta) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Protein kinase C alpha type
(Homo sapiens (Human)) | BDBM50287087
(CHEMBL21078 | N-[4-Methyl-3-(4-thiophen-2-yl-pyrim...)Show SMILES Cc1ccc(NC(=O)c2ccccc2)cc1Nc1nccc(n1)-c1cccs1 Show InChI InChI=1S/C22H18N4OS/c1-15-9-10-17(24-21(27)16-6-3-2-4-7-16)14-19(15)26-22-23-12-11-18(25-22)20-8-5-13-28-20/h2-14H,1H3,(H,24,27)(H,23,25,26) | PDB
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| n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of serine/threonine kinase(PKC-alpha) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Epidermal growth factor receptor
(Homo sapiens (Human)) | BDBM50287098
(CHEMBL21079 | N-{4-Methyl-3-[4-(1-oxy-pyridin-3-yl...)Show SMILES Cc1ccc(NC(=O)c2ccccc2)cc1Nc1nccc(n1)-c1ccc[n+]([O-])c1 Show InChI InChI=1S/C23H19N5O2/c1-16-9-10-19(25-22(29)17-6-3-2-4-7-17)14-21(16)27-23-24-12-11-20(26-23)18-8-5-13-28(30)15-18/h2-15H,1H3,(H,25,29)(H,24,26,27) | PDB
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| n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of tyrosine kinase Epidermal growth factor receptor |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Epidermal growth factor receptor
(Homo sapiens (Human)) | BDBM50240407
(CHEMBL20926 | N-(4-methyl-3-(4-(pyridin-3-yl)pyrim...)Show SMILES Cc1ccc(NC(=O)c2ccccc2)cc1Nc1nccc(n1)-c1cccnc1 Show InChI InChI=1S/C23H19N5O/c1-16-9-10-19(26-22(29)17-6-3-2-4-7-17)14-21(16)28-23-25-13-11-20(27-23)18-8-5-12-24-15-18/h2-15H,1H3,(H,26,29)(H,25,27,28) | PDB
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TBA
Curated by ChEMBL
| Assay Description
Inhibition of tyrosine kinase Epidermal growth factor receptor |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
cAMP-dependent protein kinase catalytic subunit alpha/beta/gamma
(Homo sapiens (Human)) | BDBM50287096
(2-Methoxy-N-[4-methyl-3-(4-pyridin-3-yl-pyrimidin-...)Show SMILES COc1ccccc1C(=O)Nc1ccc(C)c(Nc2nccc(n2)-c2cccnc2)c1 Show InChI InChI=1S/C24H21N5O2/c1-16-9-10-18(27-23(30)19-7-3-4-8-22(19)31-2)14-21(16)29-24-26-13-11-20(28-24)17-6-5-12-25-15-17/h3-15H,1-2H3,(H,27,30)(H,26,28,29) | PDB
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TBA
Curated by ChEMBL
| Assay Description
Inhibition of tyrosine kinase(PDGF-R) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
cAMP-dependent protein kinase catalytic subunit alpha/beta/gamma
(Homo sapiens (Human)) | BDBM50287098
(CHEMBL21079 | N-{4-Methyl-3-[4-(1-oxy-pyridin-3-yl...)Show SMILES Cc1ccc(NC(=O)c2ccccc2)cc1Nc1nccc(n1)-c1ccc[n+]([O-])c1 Show InChI InChI=1S/C23H19N5O2/c1-16-9-10-19(25-22(29)17-6-3-2-4-7-17)14-21(16)27-23-24-12-11-20(26-23)18-8-5-13-28(30)15-18/h2-15H,1H3,(H,25,29)(H,24,26,27) | PDB
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TBA
Curated by ChEMBL
| Assay Description
Inhibition of serine/threonine kinase(PKA) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
cAMP-dependent protein kinase catalytic subunit alpha/beta/gamma
(Homo sapiens (Human)) | BDBM50240407
(CHEMBL20926 | N-(4-methyl-3-(4-(pyridin-3-yl)pyrim...)Show SMILES Cc1ccc(NC(=O)c2ccccc2)cc1Nc1nccc(n1)-c1cccnc1 Show InChI InChI=1S/C23H19N5O/c1-16-9-10-19(26-22(29)17-6-3-2-4-7-17)14-21(16)28-23-25-13-11-20(27-23)18-8-5-12-24-15-18/h2-15H,1H3,(H,26,29)(H,25,27,28) | PDB
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TBA
Curated by ChEMBL
| Assay Description
Inhibition of serine/threonine kinase(PKA) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
cAMP-dependent protein kinase catalytic subunit alpha/beta/gamma
(Homo sapiens (Human)) | BDBM50240406
(CHEMBL423288 | N-(4-methyl-3-(4-(pyridin-3-yl)pyri...)Show InChI InChI=1S/C18H17N5O/c1-12-5-6-15(21-13(2)24)10-17(12)23-18-20-9-7-16(22-18)14-4-3-8-19-11-14/h3-11H,1-2H3,(H,21,24)(H,20,22,23) | PDB
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TBA
Curated by ChEMBL
| Assay Description
Inhibition of serine/threonine kinase(PKA) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Protein kinase C delta type
(Homo sapiens (Human)) | BDBM50287091
(CHEMBL20252 | Naphthalene-2-carboxylic acid [4-met...)Show SMILES Cc1ccc(NC(=O)c2ccc3ccccc3c2)cc1Nc1nccc(n1)-c1cccnc1 Show InChI InChI=1S/C27H21N5O/c1-18-8-11-23(30-26(33)21-10-9-19-5-2-3-6-20(19)15-21)16-25(18)32-27-29-14-12-24(31-27)22-7-4-13-28-17-22/h2-17H,1H3,(H,30,33)(H,29,31,32) | PDB
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TBA
Curated by ChEMBL
| Assay Description
Inhibition of serine/threonine kinase(PKC-delta) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Protein kinase C delta type
(Homo sapiens (Human)) | BDBM50287090
(4-Chloro-N-[4-methyl-3-(4-pyridin-3-yl-pyrimidin-2...)Show SMILES Cc1ccc(NC(=O)c2ccc(Cl)cc2)cc1Nc1nccc(n1)-c1cccnc1 Show InChI InChI=1S/C23H18ClN5O/c1-15-4-9-19(27-22(30)16-5-7-18(24)8-6-16)13-21(15)29-23-26-12-10-20(28-23)17-3-2-11-25-14-17/h2-14H,1H3,(H,27,30)(H,26,28,29) | PDB
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| n/a | n/a | >5.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of serine/threonine kinase(PKC-delta) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
cAMP-dependent protein kinase catalytic subunit alpha/beta/gamma
(Homo sapiens (Human)) | BDBM50287095
(4,N*1*-Dimethyl-N*3*-(4-pyridin-3-yl-pyrimidin-2-y...)Show InChI InChI=1S/C17H17N5/c1-12-5-6-14(18-2)10-16(12)22-17-20-9-7-15(21-17)13-4-3-8-19-11-13/h3-11,18H,1-2H3,(H,20,21,22) | PDB
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TBA
Curated by ChEMBL
| Assay Description
Inhibition of serine/threonine kinase(PKA) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
cAMP-dependent protein kinase catalytic subunit alpha/beta/gamma
(Homo sapiens (Human)) | BDBM50287093
((2-Methyl-5-nitro-phenyl)-(4-pyridin-3-yl-pyrimidi...)Show SMILES Cc1ccc(cc1Nc1nccc(n1)-c1cccnc1)[N+]([O-])=O Show InChI InChI=1S/C16H13N5O2/c1-11-4-5-13(21(22)23)9-15(11)20-16-18-8-6-14(19-16)12-3-2-7-17-10-12/h2-10H,1H3,(H,18,19,20) | PDB
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TBA
Curated by ChEMBL
| Assay Description
Inhibition of tyrosine kinase(PDGF-R) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Protein kinase C delta type
(Homo sapiens (Human)) | BDBM50287096
(2-Methoxy-N-[4-methyl-3-(4-pyridin-3-yl-pyrimidin-...)Show SMILES COc1ccccc1C(=O)Nc1ccc(C)c(Nc2nccc(n2)-c2cccnc2)c1 Show InChI InChI=1S/C24H21N5O2/c1-16-9-10-18(27-23(30)19-7-3-4-8-22(19)31-2)14-21(16)29-24-26-13-11-20(28-24)17-6-5-12-25-15-17/h3-15H,1-2H3,(H,27,30)(H,26,28,29) | PDB
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| n/a | n/a | >5.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of serine/threonine kinase(PKC-delta) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
cAMP-dependent protein kinase catalytic subunit alpha/beta/gamma
(Homo sapiens (Human)) | BDBM50287097
(4-Methyl-N*3*-(4-pyridin-3-yl-pyrimidin-2-yl)-benz...)Show InChI InChI=1S/C16H15N5/c1-11-4-5-13(17)9-15(11)21-16-19-8-6-14(20-16)12-3-2-7-18-10-12/h2-10H,17H2,1H3,(H,19,20,21) | PDB
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| n/a | n/a | >5.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of tyrosine kinase(PDGF-R) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
cAMP-dependent protein kinase catalytic subunit alpha/beta/gamma
(Homo sapiens (Human)) | BDBM50287088
(CHEMBL21086 | N-[4-Methoxy-3-(4-pyridin-3-yl-pyrim...)Show SMILES COc1ccc(NC(=O)c2ccccc2)cc1Nc1nccc(n1)-c1cccnc1 Show InChI InChI=1S/C23H19N5O2/c1-30-21-10-9-18(26-22(29)16-6-3-2-4-7-16)14-20(21)28-23-25-13-11-19(27-23)17-8-5-12-24-15-17/h2-15H,1H3,(H,26,29)(H,25,27,28) | PDB
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| n/a | n/a | >5.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of tyrosine kinase(PDGF-R) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Protein kinase C delta type
(Homo sapiens (Human)) | BDBM50175491
(4-Methyl-N-[4-methyl-3-(4-pyridin-3-yl-pyrimidin-2...)Show SMILES Cc1ccc(cc1)C(=O)Nc1ccc(C)c(Nc2nccc(n2)-c2cccnc2)c1 Show InChI InChI=1S/C24H21N5O/c1-16-5-8-18(9-6-16)23(30)27-20-10-7-17(2)22(14-20)29-24-26-13-11-21(28-24)19-4-3-12-25-15-19/h3-15H,1-2H3,(H,27,30)(H,26,28,29) | PDB
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| n/a | n/a | >5.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of serine/threonine kinase(PKC-delta) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
cAMP-dependent protein kinase catalytic subunit alpha/beta/gamma
(Homo sapiens (Human)) | BDBM50287092
(CHEMBL277430 | N-Benzoyl-N-[4-methyl-3-(4-pyridin-...)Show SMILES Cc1ccc(cc1Nc1nccc(n1)-c1cccnc1)N(C(=O)c1ccccc1)C(=O)c1ccccc1 Show InChI InChI=1S/C30H23N5O2/c1-21-14-15-25(19-27(21)34-30-32-18-16-26(33-30)24-13-8-17-31-20-24)35(28(36)22-9-4-2-5-10-22)29(37)23-11-6-3-7-12-23/h2-20H,1H3,(H,32,33,34) | PDB
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| n/a | n/a | >5.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of serine/threonine kinase(PKA) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Protein kinase C alpha type
(Homo sapiens (Human)) | BDBM50287093
((2-Methyl-5-nitro-phenyl)-(4-pyridin-3-yl-pyrimidi...)Show SMILES Cc1ccc(cc1Nc1nccc(n1)-c1cccnc1)[N+]([O-])=O Show InChI InChI=1S/C16H13N5O2/c1-11-4-5-13(21(22)23)9-15(11)20-16-18-8-6-14(19-16)12-3-2-7-17-10-12/h2-10H,1H3,(H,18,19,20) | PDB
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| n/a | n/a | >5.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of serine/threonine kinase(PKC-alpha) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Protein kinase C delta type
(Homo sapiens (Human)) | BDBM50287093
((2-Methyl-5-nitro-phenyl)-(4-pyridin-3-yl-pyrimidi...)Show SMILES Cc1ccc(cc1Nc1nccc(n1)-c1cccnc1)[N+]([O-])=O Show InChI InChI=1S/C16H13N5O2/c1-11-4-5-13(21(22)23)9-15(11)20-16-18-8-6-14(19-16)12-3-2-7-17-10-12/h2-10H,1H3,(H,18,19,20) | PDB
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| n/a | n/a | >5.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of serine/threonine kinase(PKC-delta) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Protein kinase C delta type
(Homo sapiens (Human)) | BDBM50287097
(4-Methyl-N*3*-(4-pyridin-3-yl-pyrimidin-2-yl)-benz...)Show InChI InChI=1S/C16H15N5/c1-11-4-5-13(17)9-15(11)21-16-19-8-6-14(20-16)12-3-2-7-18-10-12/h2-10H,17H2,1H3,(H,19,20,21) | PDB
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| n/a | n/a | >5.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of serine/threonine kinase(PKC-delta) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
cAMP-dependent protein kinase catalytic subunit alpha/beta/gamma
(Homo sapiens (Human)) | BDBM50175493
(CHEMBL277931 | N-[3-(4-Pyridin-3-yl-pyrimidin-2-yl...)Show SMILES O=C(Nc1cccc(Nc2nccc(n2)-c2cccnc2)c1)c1ccccc1 Show InChI InChI=1S/C22H17N5O/c28-21(16-6-2-1-3-7-16)25-18-9-4-10-19(14-18)26-22-24-13-11-20(27-22)17-8-5-12-23-15-17/h1-15H,(H,25,28)(H,24,26,27) | PDB
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| n/a | n/a | >5.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of tyrosine kinase(PDGF-R) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Protein kinase C delta type
(Homo sapiens (Human)) | BDBM50240407
(CHEMBL20926 | N-(4-methyl-3-(4-(pyridin-3-yl)pyrim...)Show SMILES Cc1ccc(NC(=O)c2ccccc2)cc1Nc1nccc(n1)-c1cccnc1 Show InChI InChI=1S/C23H19N5O/c1-16-9-10-19(26-22(29)17-6-3-2-4-7-17)14-21(16)28-23-25-13-11-20(27-23)18-8-5-12-24-15-18/h2-15H,1H3,(H,26,29)(H,25,27,28) | PDB
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| n/a | n/a | >5.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of serine/threonine kinase(PKC-delta) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
cAMP-dependent protein kinase catalytic subunit alpha/beta/gamma
(Homo sapiens (Human)) | BDBM50287087
(CHEMBL21078 | N-[4-Methyl-3-(4-thiophen-2-yl-pyrim...)Show SMILES Cc1ccc(NC(=O)c2ccccc2)cc1Nc1nccc(n1)-c1cccs1 Show InChI InChI=1S/C22H18N4OS/c1-15-9-10-17(24-21(27)16-6-3-2-4-7-16)14-19(15)26-22-23-12-11-18(25-22)20-8-5-13-28-20/h2-14H,1H3,(H,24,27)(H,23,25,26) | PDB
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| n/a | n/a | >5.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of serine/threonine kinase(PKA) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
cAMP-dependent protein kinase catalytic subunit alpha/beta/gamma
(Homo sapiens (Human)) | BDBM50287094
(CHEMBL278630 | N-[4-Chloro-3-(4-pyridin-3-yl-pyrim...)Show SMILES Clc1ccc(NC(=O)c2ccccc2)cc1Nc1nccc(n1)-c1cccnc1 Show InChI InChI=1S/C22H16ClN5O/c23-18-9-8-17(26-21(29)15-5-2-1-3-6-15)13-20(18)28-22-25-12-10-19(27-22)16-7-4-11-24-14-16/h1-14H,(H,26,29)(H,25,27,28) | PDB
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| n/a | n/a | >5.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of tyrosine kinase(PDGF-R) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
cAMP-dependent protein kinase catalytic subunit alpha/beta/gamma
(Homo sapiens (Human)) | BDBM50287089
(CHEMBL278287 | N-Methyl-N-[4-methyl-3-(4-pyridin-3...)Show SMILES CN(C(=O)c1ccccc1)c1ccc(C)c(Nc2nccc(n2)-c2cccnc2)c1 Show InChI InChI=1S/C24H21N5O/c1-17-10-11-20(29(2)23(30)18-7-4-3-5-8-18)15-22(17)28-24-26-14-12-21(27-24)19-9-6-13-25-16-19/h3-16H,1-2H3,(H,26,27,28) | PDB
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TBA
Curated by ChEMBL
| Assay Description
Inhibition of serine/threonine kinase(PKA) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
Protein kinase C delta type
(Homo sapiens (Human)) | BDBM50240406
(CHEMBL423288 | N-(4-methyl-3-(4-(pyridin-3-yl)pyri...)Show InChI InChI=1S/C18H17N5O/c1-12-5-6-15(21-13(2)24)10-17(12)23-18-20-9-7-16(22-18)14-4-3-8-19-11-14/h3-11H,1-2H3,(H,21,24)(H,20,22,23) | PDB
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| n/a | n/a | >5.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of serine/threonine kinase(PKC-delta) |
Bioorg Med Chem Lett 6: 1221-1226 (1996)
Article DOI: 10.1016/0960-894X(96)00197-7
BindingDB Entry DOI: 10.7270/Q2348KBG |
More data for this
Ligand-Target Pair | |
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