Found 8 hits for monomerid = 50290429 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)) | BDBM50290429
(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) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt UniProtKB/TrEMBL
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article
| n/a | n/a | 320 | n/a | n/a | n/a | n/a | n/a | n/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
(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) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| 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 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
(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) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt UniProtKB/TrEMBL
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| 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 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
(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) | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article
| n/a | n/a | 1.00E+3 | n/a | n/a | n/a | n/a | n/a | n/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
(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) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt UniProtKB/TrEMBL
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article
| n/a | n/a | 1.90E+3 | n/a | n/a | n/a | n/a | n/a | n/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
(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) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt UniProtKB/TrEMBL
B.MOAD DrugBank antibodypedia antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 1.91E+3 | n/a | n/a | n/a | n/a | n/a | n/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
(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) | PDB
KEGG
UniProtKB/SwissProt UniProtKB/TrEMBL
B.MOAD antibodypedia antibodypedia antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| 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 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
(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) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| 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 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 | |