Found 7 hits for monomerid = 50332083 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 |
Mitogen-activated protein kinase 8
(Homo sapiens (Human)) | BDBM50332083
(2-(4-methoxyphenyl)-N-(2-(2-methyl-1H-imidazol-4-y...)Show InChI InChI=1S/C17H17N3O2S/c1-11-18-10-15(19-11)17-14(7-8-23-17)20-16(21)9-12-3-5-13(22-2)6-4-12/h3-8,10H,9H2,1-2H3,(H,18,19)(H,20,21) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | 2.34E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Elan Pharmaceuticals
Curated by ChEMBL
| Assay Description Inhibition of recombinant JNK1 after 60 mins by TR-FRET assay |
Bioorg Med Chem Lett 20: 7303-7 (2010)
Article DOI: 10.1016/j.bmcl.2010.10.066 BindingDB Entry DOI: 10.7270/Q20865JW |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 9
(Homo sapiens (Human)) | BDBM50332083
(2-(4-methoxyphenyl)-N-(2-(2-methyl-1H-imidazol-4-y...)Show InChI InChI=1S/C17H17N3O2S/c1-11-18-10-15(19-11)17-14(7-8-23-17)20-16(21)9-12-3-5-13(22-2)6-4-12/h3-8,10H,9H2,1-2H3,(H,18,19)(H,20,21) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Elan Pharmaceuticals
Curated by ChEMBL
| Assay Description Inhibition of recombinant JNK2 after 60 mins by TR-FRET assay |
Bioorg Med Chem Lett 20: 7303-7 (2010)
Article DOI: 10.1016/j.bmcl.2010.10.066 BindingDB Entry DOI: 10.7270/Q20865JW |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 10
(Homo sapiens (Human)) | BDBM50332083
(2-(4-methoxyphenyl)-N-(2-(2-methyl-1H-imidazol-4-y...)Show InChI InChI=1S/C17H17N3O2S/c1-11-18-10-15(19-11)17-14(7-8-23-17)20-16(21)9-12-3-5-13(22-2)6-4-12/h3-8,10H,9H2,1-2H3,(H,18,19)(H,20,21) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | 2.70E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Elan Pharmaceuticals
Curated by ChEMBL
| Assay Description Inhibition of recombinant JNK3 after 60 mins by TR-FRET assay |
Bioorg Med Chem Lett 20: 7303-7 (2010)
Article DOI: 10.1016/j.bmcl.2010.10.066 BindingDB Entry DOI: 10.7270/Q20865JW |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 8
(Homo sapiens (Human)) | BDBM50332083
(2-(4-methoxyphenyl)-N-(2-(2-methyl-1H-imidazol-4-y...)Show InChI InChI=1S/C17H17N3O2S/c1-11-18-10-15(19-11)17-14(7-8-23-17)20-16(21)9-12-3-5-13(22-2)6-4-12/h3-8,10H,9H2,1-2H3,(H,18,19)(H,20,21) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| US Patent
| n/a | n/a | >1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
IMAGO PHARMACEUTICALS, INC.
US Patent
| Assay Description (1) Assay buffer #1 with 0.0025% Tween and 1 mM DTT was prepared using JNK buffer stock solution.(2) Assay buffer #2 with 0.025% BSA was prepared usi... |
US Patent US9796706 (2017)
BindingDB Entry DOI: 10.7270/Q24T6MHK |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 14
(Homo sapiens (Human)) | BDBM50332083
(2-(4-methoxyphenyl)-N-(2-(2-methyl-1H-imidazol-4-y...)Show InChI InChI=1S/C17H17N3O2S/c1-11-18-10-15(19-11)17-14(7-8-23-17)20-16(21)9-12-3-5-13(22-2)6-4-12/h3-8,10H,9H2,1-2H3,(H,18,19)(H,20,21) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Elan Pharmaceuticals
Curated by ChEMBL
| Assay Description Inhibition of recombinant p38alpha after 60 mins by TR-FRET assay |
Bioorg Med Chem Lett 20: 7303-7 (2010)
Article DOI: 10.1016/j.bmcl.2010.10.066 BindingDB Entry DOI: 10.7270/Q20865JW |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 10
(Homo sapiens (Human)) | BDBM50332083
(2-(4-methoxyphenyl)-N-(2-(2-methyl-1H-imidazol-4-y...)Show InChI InChI=1S/C17H17N3O2S/c1-11-18-10-15(19-11)17-14(7-8-23-17)20-16(21)9-12-3-5-13(22-2)6-4-12/h3-8,10H,9H2,1-2H3,(H,18,19)(H,20,21) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| US Patent
| n/a | n/a | >1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
IMAGO PHARMACEUTICALS, INC.
US Patent
| Assay Description (1) Assay buffer #1 with 0.0025% Tween and 1 mM DTT was prepared using JNK buffer stock solution.(2) Assay buffer #2 with 0.025% BSA was prepared usi... |
US Patent US9796706 (2017)
BindingDB Entry DOI: 10.7270/Q24T6MHK |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 1
(Homo sapiens (Human)) | BDBM50332083
(2-(4-methoxyphenyl)-N-(2-(2-methyl-1H-imidazol-4-y...)Show InChI InChI=1S/C17H17N3O2S/c1-11-18-10-15(19-11)17-14(7-8-23-17)20-16(21)9-12-3-5-13(22-2)6-4-12/h3-8,10H,9H2,1-2H3,(H,18,19)(H,20,21) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Elan Pharmaceuticals
Curated by ChEMBL
| Assay Description Inhibition of recombinant Erk2 after 60 mins by TR-FRET assay |
Bioorg Med Chem Lett 20: 7303-7 (2010)
Article DOI: 10.1016/j.bmcl.2010.10.066 BindingDB Entry DOI: 10.7270/Q20865JW |
More data for this Ligand-Target Pair | |