Found 152 hits with Last Name = 'carlson' and Initial = 'cb' 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 |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
(Homo sapiens (Human)) | BDBM50333027
(3-(Pyridin-4-ylethynyl)-1H-indazole | CHEMBL163189...)Show InChI InChI=1S/C14H9N3/c1-2-4-13-12(3-1)14(17-16-13)6-5-11-7-9-15-10-8-11/h1-4,7-10H,(H,16,17) | 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 | 360 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description Inhibition of PI3Kalpha by LanthaScreen Eu kinase binding assay |
J Med Chem 53: 8368-8375 (2010)
Article DOI: 10.1021/jm100825h BindingDB Entry DOI: 10.7270/Q2NP24PS |
More data for this Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
(Homo sapiens (Human)) | BDBM50333031
(4-((1H-Indazol-3-yl)ethynyl)aniline | CHEMBL163188...)Show InChI InChI=1S/C15H11N3/c16-12-8-5-11(6-9-12)7-10-15-13-3-1-2-4-14(13)17-18-15/h1-6,8-9H,16H2,(H,17,18) | 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 | 1.05E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description Inhibition of PI3Kalpha by LanthaScreen Eu kinase binding assay |
J Med Chem 53: 8368-8375 (2010)
Article DOI: 10.1021/jm100825h BindingDB Entry DOI: 10.7270/Q2NP24PS |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 8
(Homo sapiens (Human)) | BDBM50342301
(2-(2-(benzo[b]thiophen-3-yl)acetamido)thiophene-3-...)Show InChI InChI=1S/C15H12N2O2S2/c16-14(19)11-5-6-20-15(11)17-13(18)7-9-8-21-12-4-2-1-3-10(9)12/h1-6,8H,7H2,(H2,16,19)(H,17,18) | 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 | 1.30E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanford-Burnham Medical Research Institute
Curated by ChEMBL
| Assay Description Inhibition of JNK1 by TR-FRET assay |
Bioorg Med Chem 19: 2582-8 (2011)
Article DOI: 10.1016/j.bmc.2011.03.017 BindingDB Entry DOI: 10.7270/Q2J966PD |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 8
(Homo sapiens (Human)) | BDBM50342302
(2-(2-(2-chlorophenyl)acetamido)thiophene-3-carboxa...)Show InChI InChI=1S/C13H11ClN2O2S/c14-10-4-2-1-3-8(10)7-11(17)16-13-9(12(15)18)5-6-19-13/h1-6H,7H2,(H2,15,18)(H,16,17) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 1.40E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanford-Burnham Medical Research Institute
Curated by ChEMBL
| Assay Description Inhibition of JNK1 by TR-FRET assay |
Bioorg Med Chem 19: 2582-8 (2011)
Article DOI: 10.1016/j.bmc.2011.03.017 BindingDB Entry DOI: 10.7270/Q2J966PD |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 8
(Homo sapiens (Human)) | BDBM50342304
(2-(2-(3-bromophenyl)acetamido)thiophene-3-carboxam...)Show InChI InChI=1S/C13H11BrN2O2S/c14-9-3-1-2-8(6-9)7-11(17)16-13-10(12(15)18)4-5-19-13/h1-6H,7H2,(H2,15,18)(H,16,17) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 1.80E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanford-Burnham Medical Research Institute
Curated by ChEMBL
| Assay Description Inhibition of JNK1 by TR-FRET assay |
Bioorg Med Chem 19: 2582-8 (2011)
Article DOI: 10.1016/j.bmc.2011.03.017 BindingDB Entry DOI: 10.7270/Q2J966PD |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 8
(Homo sapiens (Human)) | BDBM50342305
(2-(2-(3-iodophenyl)acetamido)thiophene-3-carboxami...)Show InChI InChI=1S/C13H11IN2O2S/c14-9-3-1-2-8(6-9)7-11(17)16-13-10(12(15)18)4-5-19-13/h1-6H,7H2,(H2,15,18)(H,16,17) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 1.80E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanford-Burnham Medical Research Institute
Curated by ChEMBL
| Assay Description Inhibition of JNK1 by TR-FRET assay |
Bioorg Med Chem 19: 2582-8 (2011)
Article DOI: 10.1016/j.bmc.2011.03.017 BindingDB Entry DOI: 10.7270/Q2J966PD |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 8
(Homo sapiens (Human)) | BDBM50342303
(2-(2-(benzo[d][1,3]dioxol-5-yl)acetamido)thiophene...)Show InChI InChI=1S/C14H12N2O4S/c15-13(18)9-3-4-21-14(9)16-12(17)6-8-1-2-10-11(5-8)20-7-19-10/h1-5H,6-7H2,(H2,15,18)(H,16,17) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 1.80E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanford-Burnham Medical Research Institute
Curated by ChEMBL
| Assay Description Inhibition of JNK1 by TR-FRET assay |
Bioorg Med Chem 19: 2582-8 (2011)
Article DOI: 10.1016/j.bmc.2011.03.017 BindingDB Entry DOI: 10.7270/Q2J966PD |
More data for this Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
(Homo sapiens (Human)) | BDBM50333028
(3-(Pyridin-3-ylethynyl)-1H-indazole | CHEMBL163189...)Show InChI InChI=1S/C14H9N3/c1-2-6-13-12(5-1)14(17-16-13)8-7-11-4-3-9-15-10-11/h1-6,9-10H,(H,16,17) | 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 | 1.85E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description Inhibition of PI3Kalpha by LanthaScreen Eu kinase binding assay |
J Med Chem 53: 8368-8375 (2010)
Article DOI: 10.1021/jm100825h BindingDB Entry DOI: 10.7270/Q2NP24PS |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 8
(Homo sapiens (Human)) | BDBM50342306
(2-(2-(4-ethoxyphenyl)acetamido)thiophene-3-carboxa...)Show InChI InChI=1S/C15H16N2O3S/c1-2-20-11-5-3-10(4-6-11)9-13(18)17-15-12(14(16)19)7-8-21-15/h3-8H,2,9H2,1H3,(H2,16,19)(H,17,18) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 1.90E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanford-Burnham Medical Research Institute
Curated by ChEMBL
| Assay Description Inhibition of JNK1 by TR-FRET assay |
Bioorg Med Chem 19: 2582-8 (2011)
Article DOI: 10.1016/j.bmc.2011.03.017 BindingDB Entry DOI: 10.7270/Q2J966PD |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 8
(Homo sapiens (Human)) | BDBM50342307
(2-(2-(9-chloro-3,4-dihydro-2H-benzo[b][1,4]dioxepi...)Show InChI InChI=1S/C16H15ClN2O4S/c17-11-6-9(7-12-14(11)23-4-1-3-22-12)8-13(20)19-16-10(15(18)21)2-5-24-16/h2,5-7H,1,3-4,8H2,(H2,18,21)(H,19,20) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 1.90E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanford-Burnham Medical Research Institute
Curated by ChEMBL
| Assay Description Inhibition of JNK1 by TR-FRET assay |
Bioorg Med Chem 19: 2582-8 (2011)
Article DOI: 10.1016/j.bmc.2011.03.017 BindingDB Entry DOI: 10.7270/Q2J966PD |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 8
(Homo sapiens (Human)) | BDBM50342308
(2-(2-(2-methoxy-5-methylphenyl)acetamido)thiophene...)Show InChI InChI=1S/C15H16N2O3S/c1-9-3-4-12(20-2)10(7-9)8-13(18)17-15-11(14(16)19)5-6-21-15/h3-7H,8H2,1-2H3,(H2,16,19)(H,17,18) | 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 | 2.30E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanford-Burnham Medical Research Institute
Curated by ChEMBL
| Assay Description Inhibition of JNK1 by TR-FRET assay |
Bioorg Med Chem 19: 2582-8 (2011)
Article DOI: 10.1016/j.bmc.2011.03.017 BindingDB Entry DOI: 10.7270/Q2J966PD |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 8
(Homo sapiens (Human)) | BDBM50342310
(2-(2-(6-(thiophen-2-yl)imidazo[2,1-b]thiazol-3-yl)...)Show InChI InChI=1S/C16H12N4O2S3/c17-14(22)10-3-5-24-15(10)19-13(21)6-9-8-25-16-18-11(7-20(9)16)12-2-1-4-23-12/h1-5,7-8H,6H2,(H2,17,22)(H,19,21) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 2.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanford-Burnham Medical Research Institute
Curated by ChEMBL
| Assay Description Inhibition of JNK1 by TR-FRET assay |
Bioorg Med Chem 19: 2582-8 (2011)
Article DOI: 10.1016/j.bmc.2011.03.017 BindingDB Entry DOI: 10.7270/Q2J966PD |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 8
(Homo sapiens (Human)) | BDBM50342311
(2-(2-(5-methylimidazo[2,1-b]thiazol-2-yl)acetamido...)Show InChI InChI=1S/C13H12N4O2S2/c1-7-5-15-13-17(7)6-8(21-13)4-10(18)16-12-9(11(14)19)2-3-20-12/h2-3,5-6H,4H2,1H3,(H2,14,19)(H,16,18) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 2.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanford-Burnham Medical Research Institute
Curated by ChEMBL
| Assay Description Inhibition of JNK1 by TR-FRET assay |
Bioorg Med Chem 19: 2582-8 (2011)
Article DOI: 10.1016/j.bmc.2011.03.017 BindingDB Entry DOI: 10.7270/Q2J966PD |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 8
(Homo sapiens (Human)) | BDBM50342309
(2-(2-(2,3-dihydro-1H-inden-5-yl)acetamido)thiophen...)Show InChI InChI=1S/C16H16N2O2S/c17-15(20)13-6-7-21-16(13)18-14(19)9-10-4-5-11-2-1-3-12(11)8-10/h4-8H,1-3,9H2,(H2,17,20)(H,18,19) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 2.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanford-Burnham Medical Research Institute
Curated by ChEMBL
| Assay Description Inhibition of JNK1 by TR-FRET assay |
Bioorg Med Chem 19: 2582-8 (2011)
Article DOI: 10.1016/j.bmc.2011.03.017 BindingDB Entry DOI: 10.7270/Q2J966PD |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 8
(Homo sapiens (Human)) | BDBM50342312
(2-(2-(3-chlorophenyl)acetamido)thiophene-3-carboxa...)Show InChI InChI=1S/C13H11ClN2O2S/c14-9-3-1-2-8(6-9)7-11(17)16-13-10(12(15)18)4-5-19-13/h1-6H,7H2,(H2,15,18)(H,16,17) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 2.60E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanford-Burnham Medical Research Institute
Curated by ChEMBL
| Assay Description Inhibition of JNK1 by TR-FRET assay |
Bioorg Med Chem 19: 2582-8 (2011)
Article DOI: 10.1016/j.bmc.2011.03.017 BindingDB Entry DOI: 10.7270/Q2J966PD |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 8
(Homo sapiens (Human)) | BDBM50342313
(2-(2-(3-methoxyphenyl)acetamido)thiophene-3-carbox...)Show InChI InChI=1S/C14H14N2O3S/c1-19-10-4-2-3-9(7-10)8-12(17)16-14-11(13(15)18)5-6-20-14/h2-7H,8H2,1H3,(H2,15,18)(H,16,17) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 2.60E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanford-Burnham Medical Research Institute
Curated by ChEMBL
| Assay Description Inhibition of JNK1 by TR-FRET assay |
Bioorg Med Chem 19: 2582-8 (2011)
Article DOI: 10.1016/j.bmc.2011.03.017 BindingDB Entry DOI: 10.7270/Q2J966PD |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 8
(Homo sapiens (Human)) | BDBM50342314
(2-(2-(3,5-dimethylphenyl)acetamido)thiophene-3-car...)Show InChI InChI=1S/C15H16N2O2S/c1-9-5-10(2)7-11(6-9)8-13(18)17-15-12(14(16)19)3-4-20-15/h3-7H,8H2,1-2H3,(H2,16,19)(H,17,18) | 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+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanford-Burnham Medical Research Institute
Curated by ChEMBL
| Assay Description Inhibition of JNK1 by TR-FRET assay |
Bioorg Med Chem 19: 2582-8 (2011)
Article DOI: 10.1016/j.bmc.2011.03.017 BindingDB Entry DOI: 10.7270/Q2J966PD |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 8
(Homo sapiens (Human)) | BDBM50342315
(2-(2-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)acetamid...)Show InChI InChI=1S/C15H14N2O4S/c16-14(19)10-3-6-22-15(10)17-13(18)8-9-1-2-11-12(7-9)21-5-4-20-11/h1-3,6-7H,4-5,8H2,(H2,16,19)(H,17,18) | 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+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanford-Burnham Medical Research Institute
Curated by ChEMBL
| Assay Description Inhibition of JNK1 by TR-FRET assay |
Bioorg Med Chem 19: 2582-8 (2011)
Article DOI: 10.1016/j.bmc.2011.03.017 BindingDB Entry DOI: 10.7270/Q2J966PD |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 8
(Homo sapiens (Human)) | BDBM50342316
(2-(2-(2-bromophenyl)acetamido)thiophene-3-carboxam...)Show InChI InChI=1S/C13H11BrN2O2S/c14-10-4-2-1-3-8(10)7-11(17)16-13-9(12(15)18)5-6-19-13/h1-6H,7H2,(H2,15,18)(H,16,17) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 2.90E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanford-Burnham Medical Research Institute
Curated by ChEMBL
| Assay Description Inhibition of JNK1 by TR-FRET assay |
Bioorg Med Chem 19: 2582-8 (2011)
Article DOI: 10.1016/j.bmc.2011.03.017 BindingDB Entry DOI: 10.7270/Q2J966PD |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 8
(Homo sapiens (Human)) | BDBM50342317
(2-(2-(4-nitrophenyl)acetamido)thiophene-3-carboxam...)Show InChI InChI=1S/C13H11N3O4S/c14-12(18)10-5-6-21-13(10)15-11(17)7-8-1-3-9(4-2-8)16(19)20/h1-6H,7H2,(H2,14,18)(H,15,17) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 2.90E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanford-Burnham Medical Research Institute
Curated by ChEMBL
| Assay Description Inhibition of JNK1 by TR-FRET assay |
Bioorg Med Chem 19: 2582-8 (2011)
Article DOI: 10.1016/j.bmc.2011.03.017 BindingDB Entry DOI: 10.7270/Q2J966PD |
More data for this Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
(Homo sapiens (Human)) | BDBM50333017
(3-(Pyridin-4-ylethynyl)-1H-pyrazolo[3,4-b]pyridine...)Show InChI InChI=1S/C13H8N4/c1-2-11-12(16-17-13(11)15-7-1)4-3-10-5-8-14-9-6-10/h1-2,5-9H,(H,15,16,17) | 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 | 3.05E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description Inhibition of PI3Kalpha by LanthaScreen Eu kinase binding assay |
J Med Chem 53: 8368-8375 (2010)
Article DOI: 10.1021/jm100825h BindingDB Entry DOI: 10.7270/Q2NP24PS |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 8
(Homo sapiens (Human)) | BDBM50342318
(2-(2-(3,5-dimethoxyphenyl)acetamido)thiophene-3-ca...)Show InChI InChI=1S/C15H16N2O4S/c1-20-10-5-9(6-11(8-10)21-2)7-13(18)17-15-12(14(16)19)3-4-22-15/h3-6,8H,7H2,1-2H3,(H2,16,19)(H,17,18) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 3.10E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanford-Burnham Medical Research Institute
Curated by ChEMBL
| Assay Description Inhibition of JNK1 by TR-FRET assay |
Bioorg Med Chem 19: 2582-8 (2011)
Article DOI: 10.1016/j.bmc.2011.03.017 BindingDB Entry DOI: 10.7270/Q2J966PD |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 8
(Homo sapiens (Human)) | BDBM50342319
(2-(2-(thiophen-2-yl)acetamido)thiophene-3-carboxam...)Show InChI InChI=1S/C11H10N2O2S2/c12-10(15)8-3-5-17-11(8)13-9(14)6-7-2-1-4-16-7/h1-5H,6H2,(H2,12,15)(H,13,14) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL PC cid PC sid UniChem
Patents
| Article PubMed
| n/a | n/a | 3.20E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanford-Burnham Medical Research Institute
Curated by ChEMBL
| Assay Description Inhibition of JNK1 by TR-FRET assay |
Bioorg Med Chem 19: 2582-8 (2011)
Article DOI: 10.1016/j.bmc.2011.03.017 BindingDB Entry DOI: 10.7270/Q2J966PD |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 8
(Homo sapiens (Human)) | BDBM50342320
(2-(2-(2-iodophenyl)acetamido)thiophene-3-carboxami...)Show InChI InChI=1S/C13H11IN2O2S/c14-10-4-2-1-3-8(10)7-11(17)16-13-9(12(15)18)5-6-19-13/h1-6H,7H2,(H2,15,18)(H,16,17) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 3.40E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanford-Burnham Medical Research Institute
Curated by ChEMBL
| Assay Description Inhibition of JNK1 by TR-FRET assay |
Bioorg Med Chem 19: 2582-8 (2011)
Article DOI: 10.1016/j.bmc.2011.03.017 BindingDB Entry DOI: 10.7270/Q2J966PD |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 8
(Homo sapiens (Human)) | BDBM50342321
(2-(2-(4-cyanophenyl)acetamido)thiophene-3-carboxam...)Show InChI InChI=1S/C14H11N3O2S/c15-8-10-3-1-9(2-4-10)7-12(18)17-14-11(13(16)19)5-6-20-14/h1-6H,7H2,(H2,16,19)(H,17,18) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 3.40E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanford-Burnham Medical Research Institute
Curated by ChEMBL
| Assay Description Inhibition of JNK1 by TR-FRET assay |
Bioorg Med Chem 19: 2582-8 (2011)
Article DOI: 10.1016/j.bmc.2011.03.017 BindingDB Entry DOI: 10.7270/Q2J966PD |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 8
(Homo sapiens (Human)) | BDBM50342323
(2-(2-(5,6,7,8-tetrahydronaphthalen-2-yl)acetamido)...)Show InChI InChI=1S/C17H18N2O2S/c18-16(21)14-7-8-22-17(14)19-15(20)10-11-5-6-12-3-1-2-4-13(12)9-11/h5-9H,1-4,10H2,(H2,18,21)(H,19,20) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 3.60E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanford-Burnham Medical Research Institute
Curated by ChEMBL
| Assay Description Inhibition of JNK1 by TR-FRET assay |
Bioorg Med Chem 19: 2582-8 (2011)
Article DOI: 10.1016/j.bmc.2011.03.017 BindingDB Entry DOI: 10.7270/Q2J966PD |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 8
(Homo sapiens (Human)) | BDBM50342322
(2-(2-phenylacetamido)thiophene-3-carboxamide | CHE...)Show InChI InChI=1S/C13H12N2O2S/c14-12(17)10-6-7-18-13(10)15-11(16)8-9-4-2-1-3-5-9/h1-7H,8H2,(H2,14,17)(H,15,16) | 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 | 3.60E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanford-Burnham Medical Research Institute
Curated by ChEMBL
| Assay Description Inhibition of JNK1 by TR-FRET assay |
Bioorg Med Chem 19: 2582-8 (2011)
Article DOI: 10.1016/j.bmc.2011.03.017 BindingDB Entry DOI: 10.7270/Q2J966PD |
More data for this Ligand-Target Pair | |
[Pyruvate dehydrogenase (acetyl-transferring)] kinase isozyme 1, mitochondrial
(Homo sapiens (Human)) | BDBM50333027
(3-(Pyridin-4-ylethynyl)-1H-indazole | CHEMBL163189...)Show InChI InChI=1S/C14H9N3/c1-2-4-13-12(3-1)14(17-16-13)6-5-11-7-9-15-10-8-11/h1-4,7-10H,(H,16,17) | PDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | 3.87E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description Inhibition of PDK1 by Z'-LYTE kinase activity assay |
J Med Chem 53: 8368-8375 (2010)
Article DOI: 10.1021/jm100825h BindingDB Entry DOI: 10.7270/Q2NP24PS |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 8
(Homo sapiens (Human)) | BDBM50342324
(2-(2-p-tolylacetamido)thiophene-3-carboxamide | CH...)Show InChI InChI=1S/C14H14N2O2S/c1-9-2-4-10(5-3-9)8-12(17)16-14-11(13(15)18)6-7-19-14/h2-7H,8H2,1H3,(H2,15,18)(H,16,17) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 4.30E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanford-Burnham Medical Research Institute
Curated by ChEMBL
| Assay Description Inhibition of JNK1 by TR-FRET assay |
Bioorg Med Chem 19: 2582-8 (2011)
Article DOI: 10.1016/j.bmc.2011.03.017 BindingDB Entry DOI: 10.7270/Q2J966PD |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 8
(Homo sapiens (Human)) | BDBM50342301
(2-(2-(benzo[b]thiophen-3-yl)acetamido)thiophene-3-...)Show InChI InChI=1S/C15H12N2O2S2/c16-14(19)11-5-6-20-15(11)17-13(18)7-9-8-21-12-4-2-1-3-10(9)12/h1-6,8H,7H2,(H2,16,19)(H,17,18) | 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 | 4.62E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanford-Burnham Medical Research Institute
Curated by ChEMBL
| Assay Description Displacement of biotin-labeled JIP1 peptide from JNK1 by DELFIA assay |
Bioorg Med Chem 19: 2582-8 (2011)
Article DOI: 10.1016/j.bmc.2011.03.017 BindingDB Entry DOI: 10.7270/Q2J966PD |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 8
(Homo sapiens (Human)) | BDBM50342325
(2-(2-(6-fluoro-4H-benzo[d][1,3]dioxin-8-yl)acetami...)Show InChI InChI=1S/C15H13FN2O4S/c16-10-3-8(13-9(4-10)6-21-7-22-13)5-12(19)18-15-11(14(17)20)1-2-23-15/h1-4H,5-7H2,(H2,17,20)(H,18,19) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 4.90E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanford-Burnham Medical Research Institute
Curated by ChEMBL
| Assay Description Inhibition of JNK1 by TR-FRET assay |
Bioorg Med Chem 19: 2582-8 (2011)
Article DOI: 10.1016/j.bmc.2011.03.017 BindingDB Entry DOI: 10.7270/Q2J966PD |
More data for this Ligand-Target Pair | |
Serine/threonine-protein kinase mTOR
(Homo sapiens (Human)) | BDBM50333031
(4-((1H-Indazol-3-yl)ethynyl)aniline | CHEMBL163188...)Show InChI InChI=1S/C15H11N3/c16-12-8-5-11(6-9-12)7-10-15-13-3-1-2-4-14(13)17-18-15/h1-6,8-9H,16H2,(H,17,18) | 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 | 4.97E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description Inhibition of mTOR by LanthaScreen Eu kinase binding assay |
J Med Chem 53: 8368-8375 (2010)
Article DOI: 10.1021/jm100825h BindingDB Entry DOI: 10.7270/Q2NP24PS |
More data for this Ligand-Target Pair | |
Serine/threonine-protein kinase mTOR
(Homo sapiens (Human)) | BDBM50333016
(3-(Pyridin-2-ylethynyl)-1H-pyrazolo[3,4-b]pyridine...)Show InChI InChI=1S/C13H8N4/c1-3-10(9-14-7-1)5-6-12-11-4-2-8-15-13(11)17-16-12/h1-4,7-9H,(H,15,16,17) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| 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 mTOR by LanthaScreen Eu kinase binding assay |
J Med Chem 53: 8368-8375 (2010)
Article DOI: 10.1021/jm100825h BindingDB Entry DOI: 10.7270/Q2NP24PS |
More data for this Ligand-Target Pair | |
Serine/threonine-protein kinase mTOR
(Homo sapiens (Human)) | BDBM50333024
(3-((1H-Indazol-3-yl)ethynyl)aniline | CHEMBL163189...)Show InChI InChI=1S/C15H11N3/c16-12-5-3-4-11(10-12)8-9-15-13-6-1-2-7-14(13)17-18-15/h1-7,10H,16H2,(H,17,18) | 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 | 5.10E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description Inhibition of mTORC1 expressed in HEK293 cells assessed as PRAS40 Ser183 phosphorylation level by LanthaScreen cellular assay |
J Med Chem 53: 8368-8375 (2010)
Article DOI: 10.1021/jm100825h BindingDB Entry DOI: 10.7270/Q2NP24PS |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 8
(Homo sapiens (Human)) | BDBM50342326
(2-(2-(4-fluorophenyl)acetamido)thiophene-3-carboxa...)Show InChI InChI=1S/C13H11FN2O2S/c14-9-3-1-8(2-4-9)7-11(17)16-13-10(12(15)18)5-6-19-13/h1-6H,7H2,(H2,15,18)(H,16,17) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 5.10E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanford-Burnham Medical Research Institute
Curated by ChEMBL
| Assay Description Inhibition of JNK1 by TR-FRET assay |
Bioorg Med Chem 19: 2582-8 (2011)
Article DOI: 10.1016/j.bmc.2011.03.017 BindingDB Entry DOI: 10.7270/Q2J966PD |
More data for this Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
(Homo sapiens (Human)) | BDBM50333024
(3-((1H-Indazol-3-yl)ethynyl)aniline | CHEMBL163189...)Show InChI InChI=1S/C15H11N3/c16-12-5-3-4-11(10-12)8-9-15-13-6-1-2-7-14(13)17-18-15/h1-7,10H,16H2,(H,17,18) | 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 | 5.12E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description Inhibition of PI3Kalpha by LanthaScreen Eu kinase binding assay |
J Med Chem 53: 8368-8375 (2010)
Article DOI: 10.1021/jm100825h BindingDB Entry DOI: 10.7270/Q2NP24PS |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 8
(Homo sapiens (Human)) | BDBM50342328
(2-(2-m-tolylacetamido)thiophene-3-carboxamide | CH...)Show InChI InChI=1S/C14H14N2O2S/c1-9-3-2-4-10(7-9)8-12(17)16-14-11(13(15)18)5-6-19-14/h2-7H,8H2,1H3,(H2,15,18)(H,16,17) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 5.40E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanford-Burnham Medical Research Institute
Curated by ChEMBL
| Assay Description Inhibition of JNK1 by TR-FRET assay |
Bioorg Med Chem 19: 2582-8 (2011)
Article DOI: 10.1016/j.bmc.2011.03.017 BindingDB Entry DOI: 10.7270/Q2J966PD |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 8
(Homo sapiens (Human)) | BDBM50342327
(2-(2-(naphthalen-1-yl)acetamido)thiophene-3-carbox...)Show InChI InChI=1S/C17H14N2O2S/c18-16(21)14-8-9-22-17(14)19-15(20)10-12-6-3-5-11-4-1-2-7-13(11)12/h1-9H,10H2,(H2,18,21)(H,19,20) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | 5.40E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanford-Burnham Medical Research Institute
Curated by ChEMBL
| Assay Description Inhibition of JNK1 by TR-FRET assay |
Bioorg Med Chem 19: 2582-8 (2011)
Article DOI: 10.1016/j.bmc.2011.03.017 BindingDB Entry DOI: 10.7270/Q2J966PD |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 8
(Homo sapiens (Human)) | BDBM50342329
(2-(2-(4-methoxyphenyl)acetamido)thiophene-3-carbox...)Show InChI InChI=1S/C14H14N2O3S/c1-19-10-4-2-9(3-5-10)8-12(17)16-14-11(13(15)18)6-7-20-14/h2-7H,8H2,1H3,(H2,15,18)(H,16,17) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 5.70E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanford-Burnham Medical Research Institute
Curated by ChEMBL
| Assay Description Inhibition of JNK1 by TR-FRET assay |
Bioorg Med Chem 19: 2582-8 (2011)
Article DOI: 10.1016/j.bmc.2011.03.017 BindingDB Entry DOI: 10.7270/Q2J966PD |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 8
(Homo sapiens (Human)) | BDBM50342330
(2-(2-(4-(trifluoromethoxy)phenyl)acetamido)thiophe...)Show InChI InChI=1S/C14H11F3N2O3S/c15-14(16,17)22-9-3-1-8(2-4-9)7-11(20)19-13-10(12(18)21)5-6-23-13/h1-6H,7H2,(H2,18,21)(H,19,20) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 5.80E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanford-Burnham Medical Research Institute
Curated by ChEMBL
| Assay Description Inhibition of JNK1 by TR-FRET assay |
Bioorg Med Chem 19: 2582-8 (2011)
Article DOI: 10.1016/j.bmc.2011.03.017 BindingDB Entry DOI: 10.7270/Q2J966PD |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 8
(Homo sapiens (Human)) | BDBM50342331
(2-(2-(2,5-difluorophenyl)acetamido)thiophene-3-car...)Show InChI InChI=1S/C13H10F2N2O2S/c14-8-1-2-10(15)7(5-8)6-11(18)17-13-9(12(16)19)3-4-20-13/h1-5H,6H2,(H2,16,19)(H,17,18) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 5.80E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanford-Burnham Medical Research Institute
Curated by ChEMBL
| Assay Description Inhibition of JNK1 by TR-FRET assay |
Bioorg Med Chem 19: 2582-8 (2011)
Article DOI: 10.1016/j.bmc.2011.03.017 BindingDB Entry DOI: 10.7270/Q2J966PD |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 8
(Homo sapiens (Human)) | BDBM50342332
(2-benzamidothiophene-3-carboxamide | CHEMBL1767238)Show InChI InChI=1S/C12H10N2O2S/c13-10(15)9-6-7-17-12(9)14-11(16)8-4-2-1-3-5-8/h1-7H,(H2,13,15)(H,14,16) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 5.90E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanford-Burnham Medical Research Institute
Curated by ChEMBL
| Assay Description Inhibition of JNK1 by TR-FRET assay |
Bioorg Med Chem 19: 2582-8 (2011)
Article DOI: 10.1016/j.bmc.2011.03.017 BindingDB Entry DOI: 10.7270/Q2J966PD |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 8
(Homo sapiens (Human)) | BDBM50342333
(2-(2-o-tolylacetamido)thiophene-3-carboxamide | CH...)Show InChI InChI=1S/C14H14N2O2S/c1-9-4-2-3-5-10(9)8-12(17)16-14-11(13(15)18)6-7-19-14/h2-7H,8H2,1H3,(H2,15,18)(H,16,17) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 6.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanford-Burnham Medical Research Institute
Curated by ChEMBL
| Assay Description Inhibition of JNK1 by TR-FRET assay |
Bioorg Med Chem 19: 2582-8 (2011)
Article DOI: 10.1016/j.bmc.2011.03.017 BindingDB Entry DOI: 10.7270/Q2J966PD |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 8
(Homo sapiens (Human)) | BDBM50342334
(2-(2-(4-(trifluoromethyl)phenyl)acetamido)thiophen...)Show InChI InChI=1S/C14H11F3N2O2S/c15-14(16,17)9-3-1-8(2-4-9)7-11(20)19-13-10(12(18)21)5-6-22-13/h1-6H,7H2,(H2,18,21)(H,19,20) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 6.40E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanford-Burnham Medical Research Institute
Curated by ChEMBL
| Assay Description Inhibition of JNK1 by TR-FRET assay |
Bioorg Med Chem 19: 2582-8 (2011)
Article DOI: 10.1016/j.bmc.2011.03.017 BindingDB Entry DOI: 10.7270/Q2J966PD |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 8
(Homo sapiens (Human)) | BDBM50342335
(2-(2-(2,6-difluorophenyl)acetamido)thiophene-3-car...)Show InChI InChI=1S/C13H10F2N2O2S/c14-9-2-1-3-10(15)8(9)6-11(18)17-13-7(12(16)19)4-5-20-13/h1-5H,6H2,(H2,16,19)(H,17,18) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 7.40E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanford-Burnham Medical Research Institute
Curated by ChEMBL
| Assay Description Inhibition of JNK1 by TR-FRET assay |
Bioorg Med Chem 19: 2582-8 (2011)
Article DOI: 10.1016/j.bmc.2011.03.017 BindingDB Entry DOI: 10.7270/Q2J966PD |
More data for this Ligand-Target Pair | |
Transcription factor Jun
(Homo sapiens (Human)) | BDBM50342301
(2-(2-(benzo[b]thiophen-3-yl)acetamido)thiophene-3-...)Show InChI InChI=1S/C15H12N2O2S2/c16-14(19)11-5-6-20-15(11)17-13(18)7-9-8-21-12-4-2-1-3-10(9)12/h1-6,8H,7H2,(H2,16,19)(H,17,18) | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | 7.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanford-Burnham Medical Research Institute
Curated by ChEMBL
| Assay Description Inhibition of TNFalpha-induced c-Jun phosphorylation in human HeLa cells by TR-FRET assay |
Bioorg Med Chem 19: 2582-8 (2011)
Article DOI: 10.1016/j.bmc.2011.03.017 BindingDB Entry DOI: 10.7270/Q2J966PD |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 8
(Homo sapiens (Human)) | BDBM50342336
(2-(2-(3-(trifluoromethyl)phenyl)acetamido)thiophen...)Show InChI InChI=1S/C14H11F3N2O2S/c15-14(16,17)9-3-1-2-8(6-9)7-11(20)19-13-10(12(18)21)4-5-22-13/h1-6H,7H2,(H2,18,21)(H,19,20) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 7.60E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanford-Burnham Medical Research Institute
Curated by ChEMBL
| Assay Description Inhibition of JNK1 by TR-FRET assay |
Bioorg Med Chem 19: 2582-8 (2011)
Article DOI: 10.1016/j.bmc.2011.03.017 BindingDB Entry DOI: 10.7270/Q2J966PD |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 8
(Homo sapiens (Human)) | BDBM50342337
(2-(2-(4-(furan-2-ylmethyl)piperazin-1-yl)acetamido...)Show InChI InChI=1S/C16H20N4O3S/c17-15(22)13-3-9-24-16(13)18-14(21)11-20-6-4-19(5-7-20)10-12-2-1-8-23-12/h1-3,8-9H,4-7,10-11H2,(H2,17,22)(H,18,21) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 7.60E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanford-Burnham Medical Research Institute
Curated by ChEMBL
| Assay Description Inhibition of JNK1 by TR-FRET assay |
Bioorg Med Chem 19: 2582-8 (2011)
Article DOI: 10.1016/j.bmc.2011.03.017 BindingDB Entry DOI: 10.7270/Q2J966PD |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 8
(Homo sapiens (Human)) | BDBM50342338
(2-(2-(pyridin-3-yl)acetamido)thiophene-3-carboxami...)Show InChI InChI=1S/C12H11N3O2S/c13-11(17)9-3-5-18-12(9)15-10(16)6-8-2-1-4-14-7-8/h1-5,7H,6H2,(H2,13,17)(H,15,16) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 8.10E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanford-Burnham Medical Research Institute
Curated by ChEMBL
| Assay Description Inhibition of JNK1 by TR-FRET assay |
Bioorg Med Chem 19: 2582-8 (2011)
Article DOI: 10.1016/j.bmc.2011.03.017 BindingDB Entry DOI: 10.7270/Q2J966PD |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 8
(Homo sapiens (Human)) | BDBM50342339
(2-(2-(3,5-difluorophenyl)acetamido)thiophene-3-car...)Show InChI InChI=1S/C13H10F2N2O2S/c14-8-3-7(4-9(15)6-8)5-11(18)17-13-10(12(16)19)1-2-20-13/h1-4,6H,5H2,(H2,16,19)(H,17,18) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 8.20E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanford-Burnham Medical Research Institute
Curated by ChEMBL
| Assay Description Inhibition of JNK1 by TR-FRET assay |
Bioorg Med Chem 19: 2582-8 (2011)
Article DOI: 10.1016/j.bmc.2011.03.017 BindingDB Entry DOI: 10.7270/Q2J966PD |
More data for this Ligand-Target Pair | |