Found 6 hits for monomerid = 50287087 Target/Host
(Institution) | Ligand | Target/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 | pH | Temp
°C |
|---|
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
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
| CHEMBL
PC cid
PC sid
UniChem
| Article
| 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)) | 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
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
| Article
| 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 | |
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
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
antibodypedia
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
| Article
| 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 | |
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
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
| Article
| 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)) | 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
KEGG
UniProtKB/SwissProt
DrugBank
antibodypedia
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
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 | |
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
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
| Article
| 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 | |
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