Found 8 hits for monomerid = 50290424 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)) | BDBM50290424
((3-Nitro-phenyl)-(4-pyridin-2-yl-pyrimidin-2-yl)-a...)Show InChI InChI=1S/C15H11N5O2/c21-20(22)12-5-3-4-11(10-12)18-15-17-9-7-14(19-15)13-6-1-2-8-16-13/h1-10H,(H,17,18,19) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| 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 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 | |
Protein kinase C delta type
(Homo sapiens (Human)) | BDBM50290424
((3-Nitro-phenyl)-(4-pyridin-2-yl-pyrimidin-2-yl)-a...)Show InChI InChI=1S/C15H11N5O2/c21-20(22)12-5-3-4-11(10-12)18-15-17-9-7-14(19-15)13-6-1-2-8-16-13/h1-10H,(H,17,18,19) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
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 | |
Epidermal growth factor receptor
(Homo sapiens (Human)) | BDBM50290424
((3-Nitro-phenyl)-(4-pyridin-2-yl-pyrimidin-2-yl)-a...)Show InChI InChI=1S/C15H11N5O2/c21-20(22)12-5-3-4-11(10-12)18-15-17-9-7-14(19-15)13-6-1-2-8-16-13/h1-10H,(H,17,18,19) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
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 | |
Platelet-derived growth factor receptor alpha/beta
(Homo sapiens (Human)) | BDBM50290424
((3-Nitro-phenyl)-(4-pyridin-2-yl-pyrimidin-2-yl)-a...)Show InChI InChI=1S/C15H11N5O2/c21-20(22)12-5-3-4-11(10-12)18-15-17-9-7-14(19-15)13-6-1-2-8-16-13/h1-10H,(H,17,18,19) | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
DrugBank antibodypedia antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
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 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 | |
Proto-oncogene tyrosine-protein kinase Src
(Homo sapiens (Human)) | BDBM50290424
((3-Nitro-phenyl)-(4-pyridin-2-yl-pyrimidin-2-yl)-a...)Show InChI InChI=1S/C15H11N5O2/c21-20(22)12-5-3-4-11(10-12)18-15-17-9-7-14(19-15)13-6-1-2-8-16-13/h1-10H,(H,17,18,19) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
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 | |
Breakpoint cluster region protein/Tyrosine-protein kinase ABL1
(Homo sapiens (Human)) | BDBM50290424
((3-Nitro-phenyl)-(4-pyridin-2-yl-pyrimidin-2-yl)-a...)Show InChI InChI=1S/C15H11N5O2/c21-20(22)12-5-3-4-11(10-12)18-15-17-9-7-14(19-15)13-6-1-2-8-16-13/h1-10H,(H,17,18,19) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | 1.20E+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 catalytic subunit alpha/beta/gamma
(Homo sapiens (Human)) | BDBM50290424
((3-Nitro-phenyl)-(4-pyridin-2-yl-pyrimidin-2-yl)-a...)Show InChI InChI=1S/C15H11N5O2/c21-20(22)12-5-3-4-11(10-12)18-15-17-9-7-14(19-15)13-6-1-2-8-16-13/h1-10H,(H,17,18,19) | PDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia antibodypedia antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
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 A. |
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)) | BDBM50290424
((3-Nitro-phenyl)-(4-pyridin-2-yl-pyrimidin-2-yl)-a...)Show InChI InChI=1S/C15H11N5O2/c21-20(22)12-5-3-4-11(10-12)18-15-17-9-7-14(19-15)13-6-1-2-8-16-13/h1-10H,(H,17,18,19) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| 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 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 | |