Found 62 hits of Enzyme Inhibition Constant Data 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 |
|---|
Mitogen-activated protein kinase 10
(Homo sapiens (Human)) | BDBM50340629
(8-methoxy-7-(1-methyl-1H-pyrazol-4-yl)-N-(4-(3-mor...)Show SMILES COc1c(ccc2cnc(Nc3ccc(cc3)-n3cnc(n3)N3CCOCC3)nc12)-c1cnn(C)c1 Show InChI InChI=1S/C25H25N9O2/c1-32-15-18(14-28-32)21-8-3-17-13-26-24(30-22(17)23(21)35-2)29-19-4-6-20(7-5-19)34-16-27-25(31-34)33-9-11-36-12-10-33/h3-8,13-16H,9-12H2,1-2H3,(H,26,29,30) | 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 | 4 | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of JNK3 by HRTF |
Bioorg Med Chem Lett 21: 1719-23 (2011)
Article DOI: 10.1016/j.bmcl.2011.01.079
BindingDB Entry DOI: 10.7270/Q2F1901V |
More data for this
Ligand-Target Pair | |
Mitogen-activated protein kinase 10
(Homo sapiens (Human)) | BDBM50340611
(CHEMBL1761566 | N-(4-(3-morpholino-1H-1,2,4-triazo...)Show SMILES C1CN(CCO1)c1ncn(n1)-c1ccc(Nc2ncc3cccc(-c4nccs4)c3n2)cc1 Show InChI InChI=1S/C23H20N8OS/c1-2-16-14-25-22(28-20(16)19(3-1)21-24-8-13-33-21)27-17-4-6-18(7-5-17)31-15-26-23(29-31)30-9-11-32-12-10-30/h1-8,13-15H,9-12H2,(H,25,27,28) | 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 | 7 | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of JNK3 by HRTF |
Bioorg Med Chem Lett 21: 1719-23 (2011)
Article DOI: 10.1016/j.bmcl.2011.01.079
BindingDB Entry DOI: 10.7270/Q2F1901V |
More data for this
Ligand-Target Pair | |
Mitogen-activated protein kinase 10
(Homo sapiens (Human)) | BDBM50340627
(7,8-bis(1-methyl-1H-pyrazol-4-yl)-N-(4-(3-morpholi...)Show SMILES Cn1cc(cn1)-c1ccc2cnc(Nc3ccc(cc3)-n3cnc(n3)N3CCOCC3)nc2c1-c1cnn(C)c1 Show InChI InChI=1S/C28H27N11O/c1-36-16-20(14-31-36)24-8-3-19-13-29-27(34-26(19)25(24)21-15-32-37(2)17-21)33-22-4-6-23(7-5-22)39-18-30-28(35-39)38-9-11-40-12-10-38/h3-8,13-18H,9-12H2,1-2H3,(H,29,33,34) | 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 | 9 | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of JNK3 by HRTF |
Bioorg Med Chem Lett 21: 1719-23 (2011)
Article DOI: 10.1016/j.bmcl.2011.01.079
BindingDB Entry DOI: 10.7270/Q2F1901V |
More data for this
Ligand-Target Pair | |
Mitogen-activated protein kinase 8
(Homo sapiens (Human)) | BDBM50340614
(CHEMBL1761569 | N-(4-(3-methyl-1H-1,2,4-triazol-1-...)Show SMILES Cc1ncn(n1)-c1ccc(Nc2ncc3cccc(-c4nccs4)c3n2)cc1 Show InChI InChI=1S/C20H15N7S/c1-13-23-12-27(26-13)16-7-5-15(6-8-16)24-20-22-11-14-3-2-4-17(18(14)25-20)19-21-9-10-28-19/h2-12H,1H3,(H,22,24,25) | 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 | 10 | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of JNK1 by HRTF |
Bioorg Med Chem Lett 21: 1719-23 (2011)
Article DOI: 10.1016/j.bmcl.2011.01.079
BindingDB Entry DOI: 10.7270/Q2F1901V |
More data for this
Ligand-Target Pair | |
Mitogen-activated protein kinase 10
(Homo sapiens (Human)) | BDBM50340624
(8-methyl-7-(1-methyl-1H-pyrazol-4-yl)-N-(4-(3-morp...)Show SMILES Cc1c(ccc2cnc(Nc3ccc(cc3)-n3cnc(n3)N3CCOCC3)nc12)-c1cnn(C)c1 Show InChI InChI=1S/C25H25N9O/c1-17-22(19-14-28-32(2)15-19)8-3-18-13-26-24(30-23(17)18)29-20-4-6-21(7-5-20)34-16-27-25(31-34)33-9-11-35-12-10-33/h3-8,13-16H,9-12H2,1-2H3,(H,26,29,30) | 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 | 10 | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of JNK3 by HRTF |
Bioorg Med Chem Lett 21: 1719-23 (2011)
Article DOI: 10.1016/j.bmcl.2011.01.079
BindingDB Entry DOI: 10.7270/Q2F1901V |
More data for this
Ligand-Target Pair | |
Mitogen-activated protein kinase 8
(Homo sapiens (Human)) | BDBM50340609
(8-(1-methyl-1H-pyrazol-4-yl)-N-(4-(3-morpholino-1H...)Show SMILES Cn1cc(cn1)-c1cccc2cnc(Nc3ccc(cc3)-n3cnc(n3)N3CCOCC3)nc12 Show InChI InChI=1S/C24H23N9O/c1-31-15-18(14-27-31)21-4-2-3-17-13-25-23(29-22(17)21)28-19-5-7-20(8-6-19)33-16-26-24(30-33)32-9-11-34-12-10-32/h2-8,13-16H,9-12H2,1H3,(H,25,28,29) | 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 | 10 | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of JNK1 by HRTF |
Bioorg Med Chem Lett 21: 1719-23 (2011)
Article DOI: 10.1016/j.bmcl.2011.01.079
BindingDB Entry DOI: 10.7270/Q2F1901V |
More data for this
Ligand-Target Pair | |
Mitogen-activated protein kinase 10
(Homo sapiens (Human)) | BDBM50340628
(7-(1-methyl-1H-pyrazol-4-yl)-N-(4-(3-morpholino-1H...)Show SMILES Cn1cc(cn1)-c1ccc2cnc(Nc3ccc(cc3)-n3cnc(n3)N3CCOCC3)nc2c1-c1ccccc1 Show InChI InChI=1S/C30H27N9O/c1-37-19-23(18-33-37)26-12-7-22-17-31-29(35-28(22)27(26)21-5-3-2-4-6-21)34-24-8-10-25(11-9-24)39-20-32-30(36-39)38-13-15-40-16-14-38/h2-12,17-20H,13-16H2,1H3,(H,31,34,35) | 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 | 10 | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of JNK3 by HRTF |
Bioorg Med Chem Lett 21: 1719-23 (2011)
Article DOI: 10.1016/j.bmcl.2011.01.079
BindingDB Entry DOI: 10.7270/Q2F1901V |
More data for this
Ligand-Target Pair | |
Mitogen-activated protein kinase 10
(Homo sapiens (Human)) | BDBM50340609
(8-(1-methyl-1H-pyrazol-4-yl)-N-(4-(3-morpholino-1H...)Show SMILES Cn1cc(cn1)-c1cccc2cnc(Nc3ccc(cc3)-n3cnc(n3)N3CCOCC3)nc12 Show InChI InChI=1S/C24H23N9O/c1-31-15-18(14-27-31)21-4-2-3-17-13-25-23(29-22(17)21)28-19-5-7-20(8-6-19)33-16-26-24(30-33)32-9-11-34-12-10-32/h2-8,13-16H,9-12H2,1H3,(H,25,28,29) | 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 | 20 | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of JNK3 by HRTF |
Bioorg Med Chem Lett 21: 1719-23 (2011)
Article DOI: 10.1016/j.bmcl.2011.01.079
BindingDB Entry DOI: 10.7270/Q2F1901V |
More data for this
Ligand-Target Pair | |
Mitogen-activated protein kinase 10
(Homo sapiens (Human)) | BDBM50340626
(8-cyclopropyl-7-(1-methyl-1H-pyrazol-4-yl)-N-(4-(3...)Show SMILES Cn1cc(cn1)-c1ccc2cnc(Nc3ccc(cc3)-n3cnc(n3)N3CCOCC3)nc2c1C1CC1 Show InChI InChI=1S/C27H27N9O/c1-34-16-20(15-30-34)23-9-4-19-14-28-26(32-25(19)24(23)18-2-3-18)31-21-5-7-22(8-6-21)36-17-29-27(33-36)35-10-12-37-13-11-35/h4-9,14-18H,2-3,10-13H2,1H3,(H,28,31,32) | 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 | 20 | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of JNK3 by HRTF |
Bioorg Med Chem Lett 21: 1719-23 (2011)
Article DOI: 10.1016/j.bmcl.2011.01.079
BindingDB Entry DOI: 10.7270/Q2F1901V |
More data for this
Ligand-Target Pair | |
Mitogen-activated protein kinase 8
(Homo sapiens (Human)) | BDBM50340608
(8-(6-methylpyridin-3-yl)-N-(4-(3-morpholino-1H-1,2...)Show SMILES Cc1ccc(cn1)-c1cccc2cnc(Nc3ccc(cc3)-n3cnc(n3)N3CCOCC3)nc12 Show InChI InChI=1S/C26H24N8O/c1-18-5-6-19(15-27-18)23-4-2-3-20-16-28-25(31-24(20)23)30-21-7-9-22(10-8-21)34-17-29-26(32-34)33-11-13-35-14-12-33/h2-10,15-17H,11-14H2,1H3,(H,28,30,31) | 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 | 20 | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of JNK1 by HRTF |
Bioorg Med Chem Lett 21: 1719-23 (2011)
Article DOI: 10.1016/j.bmcl.2011.01.079
BindingDB Entry DOI: 10.7270/Q2F1901V |
More data for this
Ligand-Target Pair | |
Transcription factor Jun
(Homo sapiens (Human)) | BDBM50340608
(8-(6-methylpyridin-3-yl)-N-(4-(3-morpholino-1H-1,2...)Show SMILES Cc1ccc(cn1)-c1cccc2cnc(Nc3ccc(cc3)-n3cnc(n3)N3CCOCC3)nc12 Show InChI InChI=1S/C26H24N8O/c1-18-5-6-19(15-27-18)23-4-2-3-20-16-28-25(31-24(20)23)30-21-7-9-22(10-8-21)34-17-29-26(32-34)33-11-13-35-14-12-33/h2-10,15-17H,11-14H2,1H3,(H,28,30,31) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 20 | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of c-Jun |
Bioorg Med Chem Lett 21: 1719-23 (2011)
Article DOI: 10.1016/j.bmcl.2011.01.079
BindingDB Entry DOI: 10.7270/Q2F1901V |
More data for this
Ligand-Target Pair | |
Mitogen-activated protein kinase 10
(Homo sapiens (Human)) | BDBM50340614
(CHEMBL1761569 | N-(4-(3-methyl-1H-1,2,4-triazol-1-...)Show SMILES Cc1ncn(n1)-c1ccc(Nc2ncc3cccc(-c4nccs4)c3n2)cc1 Show InChI InChI=1S/C20H15N7S/c1-13-23-12-27(26-13)16-7-5-15(6-8-16)24-20-22-11-14-3-2-4-17(18(14)25-20)19-21-9-10-28-19/h2-12H,1H3,(H,22,24,25) | 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 | 20 | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of JNK3 by HRTF |
Bioorg Med Chem Lett 21: 1719-23 (2011)
Article DOI: 10.1016/j.bmcl.2011.01.079
BindingDB Entry DOI: 10.7270/Q2F1901V |
More data for this
Ligand-Target Pair | |
Mitogen-activated protein kinase 10
(Homo sapiens (Human)) | BDBM50340608
(8-(6-methylpyridin-3-yl)-N-(4-(3-morpholino-1H-1,2...)Show SMILES Cc1ccc(cn1)-c1cccc2cnc(Nc3ccc(cc3)-n3cnc(n3)N3CCOCC3)nc12 Show InChI InChI=1S/C26H24N8O/c1-18-5-6-19(15-27-18)23-4-2-3-20-16-28-25(31-24(20)23)30-21-7-9-22(10-8-21)34-17-29-26(32-34)33-11-13-35-14-12-33/h2-10,15-17H,11-14H2,1H3,(H,28,30,31) | 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 | 30 | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of JNK3 by HRTF |
Bioorg Med Chem Lett 21: 1719-23 (2011)
Article DOI: 10.1016/j.bmcl.2011.01.079
BindingDB Entry DOI: 10.7270/Q2F1901V |
More data for this
Ligand-Target Pair | |
Mitogen-activated protein kinase 8
(Homo sapiens (Human)) | BDBM50340611
(CHEMBL1761566 | N-(4-(3-morpholino-1H-1,2,4-triazo...)Show SMILES C1CN(CCO1)c1ncn(n1)-c1ccc(Nc2ncc3cccc(-c4nccs4)c3n2)cc1 Show InChI InChI=1S/C23H20N8OS/c1-2-16-14-25-22(28-20(16)19(3-1)21-24-8-13-33-21)27-17-4-6-18(7-5-17)31-15-26-23(29-31)30-9-11-32-12-10-30/h1-8,13-15H,9-12H2,(H,25,27,28) | 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 | 30 | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of JNK1 by HRTF |
Bioorg Med Chem Lett 21: 1719-23 (2011)
Article DOI: 10.1016/j.bmcl.2011.01.079
BindingDB Entry DOI: 10.7270/Q2F1901V |
More data for this
Ligand-Target Pair | |
Mitogen-activated protein kinase 10
(Homo sapiens (Human)) | BDBM50340621
(((cis)-4-(8-(6-methylpyridin-3-yl)quinazolin-2-yla...)Show SMILES Cc1ccc(cn1)-c1cccc2cnc(N[C@H]3CC[C@H](CC3)C(=O)N3CCCC3)nc12 |r,wU:16.16,19.23,(12,-17.01,;10.66,-17.78,;10.65,-19.32,;9.32,-20.08,;7.99,-19.31,;7.99,-17.77,;9.33,-17,;6.66,-20.07,;5.32,-19.29,;3.99,-20.07,;3.99,-21.62,;5.32,-22.38,;5.3,-23.92,;6.64,-24.71,;7.98,-23.94,;9.31,-24.72,;10.65,-23.97,;10.65,-22.42,;12,-21.67,;13.33,-22.46,;13.31,-24,;11.97,-24.75,;14.67,-21.7,;14.69,-20.16,;16,-22.49,;15.98,-24.02,;17.44,-24.52,;18.36,-23.28,;17.47,-22.03,;8,-22.39,;6.66,-21.62,)| Show InChI InChI=1S/C25H29N5O/c1-17-7-8-19(15-26-17)22-6-4-5-20-16-27-25(29-23(20)22)28-21-11-9-18(10-12-21)24(31)30-13-2-3-14-30/h4-8,15-16,18,21H,2-3,9-14H2,1H3,(H,27,28,29)/t18-,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 | 30 | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of JNK3 by HRTF |
Bioorg Med Chem Lett 21: 1719-23 (2011)
Article DOI: 10.1016/j.bmcl.2011.01.079
BindingDB Entry DOI: 10.7270/Q2F1901V |
More data for this
Ligand-Target Pair | |
Mitogen-activated protein kinase 10
(Homo sapiens (Human)) | BDBM50340616
(CHEMBL1761571 | N-(4-(3-methyl-1H-1,2,4-triazol-1-...)Show SMILES Cc1ncn(n1)-c1ccc(Nc2ncc3cccc(-c4ccc(C)nc4)c3n2)cc1 Show InChI InChI=1S/C23H19N7/c1-15-6-7-17(12-24-15)21-5-3-4-18-13-25-23(28-22(18)21)27-19-8-10-20(11-9-19)30-14-26-16(2)29-30/h3-14H,1-2H3,(H,25,27,28) | 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 | 30 | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of JNK3 by HRTF |
Bioorg Med Chem Lett 21: 1719-23 (2011)
Article DOI: 10.1016/j.bmcl.2011.01.079
BindingDB Entry DOI: 10.7270/Q2F1901V |
More data for this
Ligand-Target Pair | |
Transcription factor Jun
(Homo sapiens (Human)) | BDBM50340606
(CHEMBL1761561 | N-(4-(3-(6-methylpyridin-3-yl)-1H-...)Show SMILES Cc1ccc(cn1)-c1ncn(n1)-c1ccc(Nc2ncc3ccc(cc3n2)-c2cn[nH]c2)cc1 Show InChI InChI=1S/C25H19N9/c1-16-2-3-19(12-26-16)24-28-15-34(33-24)22-8-6-21(7-9-22)31-25-27-11-18-5-4-17(10-23(18)32-25)20-13-29-30-14-20/h2-15H,1H3,(H,29,30)(H,27,31,32) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | 40 | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of c-Jun |
Bioorg Med Chem Lett 21: 1719-23 (2011)
Article DOI: 10.1016/j.bmcl.2011.01.079
BindingDB Entry DOI: 10.7270/Q2F1901V |
More data for this
Ligand-Target Pair | |
Transcription factor Jun
(Homo sapiens (Human)) | BDBM50340628
(7-(1-methyl-1H-pyrazol-4-yl)-N-(4-(3-morpholino-1H...)Show SMILES Cn1cc(cn1)-c1ccc2cnc(Nc3ccc(cc3)-n3cnc(n3)N3CCOCC3)nc2c1-c1ccccc1 Show InChI InChI=1S/C30H27N9O/c1-37-19-23(18-33-37)26-12-7-22-17-31-29(35-28(22)27(26)21-5-3-2-4-6-21)34-24-8-10-25(11-9-24)39-20-32-30(36-39)38-13-15-40-16-14-38/h2-12,17-20H,13-16H2,1H3,(H,31,34,35) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 40 | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of c-Jun |
Bioorg Med Chem Lett 21: 1719-23 (2011)
Article DOI: 10.1016/j.bmcl.2011.01.079
BindingDB Entry DOI: 10.7270/Q2F1901V |
More data for this
Ligand-Target Pair | |
Mitogen-activated protein kinase 10
(Homo sapiens (Human)) | BDBM50340622
(8-chloro-7-(1-methyl-1H-pyrazol-4-yl)-N-(4-(3-morp...)Show SMILES Cn1cc(cn1)-c1ccc2cnc(Nc3ccc(cc3)-n3cnc(n3)N3CCOCC3)nc2c1Cl Show InChI InChI=1S/C24H22ClN9O/c1-32-14-17(13-28-32)20-7-2-16-12-26-23(30-22(16)21(20)25)29-18-3-5-19(6-4-18)34-15-27-24(31-34)33-8-10-35-11-9-33/h2-7,12-15H,8-11H2,1H3,(H,26,29,30) | 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 | 40 | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of JNK3 by HRTF |
Bioorg Med Chem Lett 21: 1719-23 (2011)
Article DOI: 10.1016/j.bmcl.2011.01.079
BindingDB Entry DOI: 10.7270/Q2F1901V |
More data for this
Ligand-Target Pair | |
Transcription factor Jun
(Homo sapiens (Human)) | BDBM50340627
(7,8-bis(1-methyl-1H-pyrazol-4-yl)-N-(4-(3-morpholi...)Show SMILES Cn1cc(cn1)-c1ccc2cnc(Nc3ccc(cc3)-n3cnc(n3)N3CCOCC3)nc2c1-c1cnn(C)c1 Show InChI InChI=1S/C28H27N11O/c1-36-16-20(14-31-36)24-8-3-19-13-29-27(34-26(19)25(24)21-15-32-37(2)17-21)33-22-4-6-23(7-5-22)39-18-30-28(35-39)38-9-11-40-12-10-38/h3-8,13-18H,9-12H2,1-2H3,(H,29,33,34) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 40 | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of c-Jun |
Bioorg Med Chem Lett 21: 1719-23 (2011)
Article DOI: 10.1016/j.bmcl.2011.01.079
BindingDB Entry DOI: 10.7270/Q2F1901V |
More data for this
Ligand-Target Pair | |
Mitogen-activated protein kinase 8
(Homo sapiens (Human)) | BDBM50340600
(CHEMBL1761555 | N-(4-(3-morpholino-1H-1,2,4-triazo...)Show SMILES C1CN(CCO1)c1ncn(n1)-c1ccc(Nc2ncc3ccc(cc3n2)-c2cn[nH]c2)cc1 Show InChI InChI=1S/C23H21N9O/c1-2-17-12-24-22(29-21(17)11-16(1)18-13-26-27-14-18)28-19-3-5-20(6-4-19)32-15-25-23(30-32)31-7-9-33-10-8-31/h1-6,11-15H,7-10H2,(H,26,27)(H,24,28,29) | 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 | 40 | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of JNK1 by HRTF |
Bioorg Med Chem Lett 21: 1719-23 (2011)
Article DOI: 10.1016/j.bmcl.2011.01.079
BindingDB Entry DOI: 10.7270/Q2F1901V |
More data for this
Ligand-Target Pair | |
Mitogen-activated protein kinase 10
(Homo sapiens (Human)) | BDBM50340606
(CHEMBL1761561 | N-(4-(3-(6-methylpyridin-3-yl)-1H-...)Show SMILES Cc1ccc(cn1)-c1ncn(n1)-c1ccc(Nc2ncc3ccc(cc3n2)-c2cn[nH]c2)cc1 Show InChI InChI=1S/C25H19N9/c1-16-2-3-19(12-26-16)24-28-15-34(33-24)22-8-6-21(7-9-22)31-25-27-11-18-5-4-17(10-23(18)32-25)20-13-29-30-14-20/h2-15H,1H3,(H,29,30)(H,27,31,32) | 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 | 50 | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of JNK3 by HRTF |
Bioorg Med Chem Lett 21: 1719-23 (2011)
Article DOI: 10.1016/j.bmcl.2011.01.079
BindingDB Entry DOI: 10.7270/Q2F1901V |
More data for this
Ligand-Target Pair | |
Transcription factor Jun
(Homo sapiens (Human)) | BDBM50340629
(8-methoxy-7-(1-methyl-1H-pyrazol-4-yl)-N-(4-(3-mor...)Show SMILES COc1c(ccc2cnc(Nc3ccc(cc3)-n3cnc(n3)N3CCOCC3)nc12)-c1cnn(C)c1 Show InChI InChI=1S/C25H25N9O2/c1-32-15-18(14-28-32)21-8-3-17-13-26-24(30-22(17)23(21)35-2)29-19-4-6-20(7-5-19)34-16-27-25(31-34)33-9-11-36-12-10-33/h3-8,13-16H,9-12H2,1-2H3,(H,26,29,30) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 50 | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of c-Jun |
Bioorg Med Chem Lett 21: 1719-23 (2011)
Article DOI: 10.1016/j.bmcl.2011.01.079
BindingDB Entry DOI: 10.7270/Q2F1901V |
More data for this
Ligand-Target Pair | |
Mitogen-activated protein kinase 10
(Homo sapiens (Human)) | BDBM50340620
(4-(8-(6-methylpyridin-3-yl)quinazolin-2-ylamino)cy...)Show SMILES Cc1ccc(cn1)-c1cccc2cnc(NC3CCC(O)CC3)nc12 |(-2.41,-16.62,;-3.75,-17.39,;-3.76,-18.93,;-5.09,-19.69,;-6.42,-18.91,;-6.42,-17.38,;-5.08,-16.61,;-7.75,-19.68,;-9.09,-18.9,;-10.42,-19.68,;-10.42,-21.22,;-9.09,-21.99,;-9.11,-23.53,;-7.78,-24.31,;-6.43,-23.55,;-5.1,-24.33,;-3.77,-23.57,;-2.44,-24.35,;-1.11,-23.6,;-1.08,-22.06,;.26,-21.31,;-2.41,-21.28,;-3.76,-22.03,;-6.42,-22,;-7.75,-21.22,)| Show InChI InChI=1S/C20H22N4O/c1-13-5-6-14(11-21-13)18-4-2-3-15-12-22-20(24-19(15)18)23-16-7-9-17(25)10-8-16/h2-6,11-12,16-17,25H,7-10H2,1H3,(H,22,23,24) | 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 | 50 | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of JNK3 by HRTF |
Bioorg Med Chem Lett 21: 1719-23 (2011)
Article DOI: 10.1016/j.bmcl.2011.01.079
BindingDB Entry DOI: 10.7270/Q2F1901V |
More data for this
Ligand-Target Pair | |
Mitogen-activated protein kinase 8
(Homo sapiens (Human)) | BDBM50340612
(CHEMBL1761567 | N-(4-(3-morpholino-1H-1,2,4-triazo...)Show SMILES C1CN(CCO1)c1ncn(n1)-c1ccc(Nc2ncc3cccc(-c4ccccc4)c3n2)cc1 Show InChI InChI=1S/C26H23N7O/c1-2-5-19(6-3-1)23-8-4-7-20-17-27-25(30-24(20)23)29-21-9-11-22(12-10-21)33-18-28-26(31-33)32-13-15-34-16-14-32/h1-12,17-18H,13-16H2,(H,27,29,30) | 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 | 50 | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of JNK1 by HRTF |
Bioorg Med Chem Lett 21: 1719-23 (2011)
Article DOI: 10.1016/j.bmcl.2011.01.079
BindingDB Entry DOI: 10.7270/Q2F1901V |
More data for this
Ligand-Target Pair | |
Mitogen-activated protein kinase 10
(Homo sapiens (Human)) | BDBM50340600
(CHEMBL1761555 | N-(4-(3-morpholino-1H-1,2,4-triazo...)Show SMILES C1CN(CCO1)c1ncn(n1)-c1ccc(Nc2ncc3ccc(cc3n2)-c2cn[nH]c2)cc1 Show InChI InChI=1S/C23H21N9O/c1-2-17-12-24-22(29-21(17)11-16(1)18-13-26-27-14-18)28-19-3-5-20(6-4-19)32-15-25-23(30-32)31-7-9-33-10-8-31/h1-6,11-15H,7-10H2,(H,26,27)(H,24,28,29) | 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 | 50 | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of JNK3 by HRTF |
Bioorg Med Chem Lett 21: 1719-23 (2011)
Article DOI: 10.1016/j.bmcl.2011.01.079
BindingDB Entry DOI: 10.7270/Q2F1901V |
More data for this
Ligand-Target Pair | |
Mitogen-activated protein kinase 8
(Homo sapiens (Human)) | BDBM50340599
(7-(1-methyl-1H-pyrazol-4-yl)-N-(4-(3-morpholino-1H...)Show SMILES Cn1cc(cn1)-c1ccc2cnc(Nc3ccc(cc3)-n3cnc(n3)N3CCOCC3)nc2c1 Show InChI InChI=1S/C24H23N9O/c1-31-15-19(14-27-31)17-2-3-18-13-25-23(29-22(18)12-17)28-20-4-6-21(7-5-20)33-16-26-24(30-33)32-8-10-34-11-9-32/h2-7,12-16H,8-11H2,1H3,(H,25,28,29) | 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 | 50 | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of JNK1 by HRTF |
Bioorg Med Chem Lett 21: 1719-23 (2011)
Article DOI: 10.1016/j.bmcl.2011.01.079
BindingDB Entry DOI: 10.7270/Q2F1901V |
More data for this
Ligand-Target Pair | |
Mitogen-activated protein kinase 10
(Homo sapiens (Human)) | BDBM50340607
(7-(1-methyl-1H-pyrazol-4-yl)-N-(4-(3-(pyridin-2-yl...)Show SMILES Cn1cc(cn1)-c1ccc2cnc(Nc3ccc(cc3)-n3cnc(n3)-c3ccccn3)nc2c1 Show InChI InChI=1S/C25H19N9/c1-33-15-19(14-29-33)17-5-6-18-13-27-25(31-23(18)12-17)30-20-7-9-21(10-8-20)34-16-28-24(32-34)22-4-2-3-11-26-22/h2-16H,1H3,(H,27,30,31) | 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 | 60 | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of JNK3 by HRTF |
Bioorg Med Chem Lett 21: 1719-23 (2011)
Article DOI: 10.1016/j.bmcl.2011.01.079
BindingDB Entry DOI: 10.7270/Q2F1901V |
More data for this
Ligand-Target Pair | |
Mitogen-activated protein kinase 10
(Homo sapiens (Human)) | BDBM50340617
(CHEMBL1761572 | N-(benzo[d][1,3]dioxol-5-yl)-8-(6-...)Show InChI InChI=1S/C21H16N4O2/c1-13-5-6-14(10-22-13)17-4-2-3-15-11-23-21(25-20(15)17)24-16-7-8-18-19(9-16)27-12-26-18/h2-11H,12H2,1H3,(H,23,24,25) | 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 | 60 | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of JNK3 by HRTF |
Bioorg Med Chem Lett 21: 1719-23 (2011)
Article DOI: 10.1016/j.bmcl.2011.01.079
BindingDB Entry DOI: 10.7270/Q2F1901V |
More data for this
Ligand-Target Pair | |
Mitogen-activated protein kinase 10
(Homo sapiens (Human)) | BDBM50340612
(CHEMBL1761567 | N-(4-(3-morpholino-1H-1,2,4-triazo...)Show SMILES C1CN(CCO1)c1ncn(n1)-c1ccc(Nc2ncc3cccc(-c4ccccc4)c3n2)cc1 Show InChI InChI=1S/C26H23N7O/c1-2-5-19(6-3-1)23-8-4-7-20-17-27-25(30-24(20)23)29-21-9-11-22(12-10-21)33-18-28-26(31-33)32-13-15-34-16-14-32/h1-12,17-18H,13-16H2,(H,27,29,30) | 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 | 60 | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of JNK3 by HRTF |
Bioorg Med Chem Lett 21: 1719-23 (2011)
Article DOI: 10.1016/j.bmcl.2011.01.079
BindingDB Entry DOI: 10.7270/Q2F1901V |
More data for this
Ligand-Target Pair | |
Mitogen-activated protein kinase 10
(Homo sapiens (Human)) | BDBM50340623
(8-chloro-7-(1-isopropyl-1H-pyrazol-4-yl)-N-(4-(3-m...)Show SMILES CC(C)n1cc(cn1)-c1ccc2cnc(Nc3ccc(cc3)-n3cnc(n3)N3CCOCC3)nc2c1Cl Show InChI InChI=1S/C26H26ClN9O/c1-17(2)35-15-19(14-30-35)22-8-3-18-13-28-25(32-24(18)23(22)27)31-20-4-6-21(7-5-20)36-16-29-26(33-36)34-9-11-37-12-10-34/h3-8,13-17H,9-12H2,1-2H3,(H,28,31,32) | 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 | 63 | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of JNK3 by HRTF |
Bioorg Med Chem Lett 21: 1719-23 (2011)
Article DOI: 10.1016/j.bmcl.2011.01.079
BindingDB Entry DOI: 10.7270/Q2F1901V |
More data for this
Ligand-Target Pair | |
Mitogen-activated protein kinase 10
(Homo sapiens (Human)) | BDBM50340610
(8-(3-fluoro-4-methoxyphenyl)-N-(4-(3-morpholino-1H...)Show SMILES COc1ccc(cc1F)-c1cccc2cnc(Nc3ccc(cc3)-n3cnc(n3)N3CCOCC3)nc12 Show InChI InChI=1S/C27H24FN7O2/c1-36-24-10-5-18(15-23(24)28)22-4-2-3-19-16-29-26(32-25(19)22)31-20-6-8-21(9-7-20)35-17-30-27(33-35)34-11-13-37-14-12-34/h2-10,15-17H,11-14H2,1H3,(H,29,31,32) | 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 | 70 | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of JNK3 by HRTF |
Bioorg Med Chem Lett 21: 1719-23 (2011)
Article DOI: 10.1016/j.bmcl.2011.01.079
BindingDB Entry DOI: 10.7270/Q2F1901V |
More data for this
Ligand-Target Pair | |
Mitogen-activated protein kinase 10
(Homo sapiens (Human)) | BDBM50340613
(8-(3-fluoro-4-methoxyphenyl)-N-(4-(3-methyl-1H-1,2...)Show SMILES COc1ccc(cc1F)-c1cccc2cnc(Nc3ccc(cc3)-n3cnc(C)n3)nc12 Show InChI InChI=1S/C24H19FN6O/c1-15-27-14-31(30-15)19-9-7-18(8-10-19)28-24-26-13-17-4-3-5-20(23(17)29-24)16-6-11-22(32-2)21(25)12-16/h3-14H,1-2H3,(H,26,28,29) | 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 | 80 | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of JNK3 by HRTF |
Bioorg Med Chem Lett 21: 1719-23 (2011)
Article DOI: 10.1016/j.bmcl.2011.01.079
BindingDB Entry DOI: 10.7270/Q2F1901V |
More data for this
Ligand-Target Pair | |
Mitogen-activated protein kinase 8
(Homo sapiens (Human)) | BDBM50340610
(8-(3-fluoro-4-methoxyphenyl)-N-(4-(3-morpholino-1H...)Show SMILES COc1ccc(cc1F)-c1cccc2cnc(Nc3ccc(cc3)-n3cnc(n3)N3CCOCC3)nc12 Show InChI InChI=1S/C27H24FN7O2/c1-36-24-10-5-18(15-23(24)28)22-4-2-3-19-16-29-26(32-25(19)22)31-20-6-8-21(9-7-20)35-17-30-27(33-35)34-11-13-37-14-12-34/h2-10,15-17H,11-14H2,1H3,(H,29,31,32) | 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 | 90 | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of JNK1 by HRTF |
Bioorg Med Chem Lett 21: 1719-23 (2011)
Article DOI: 10.1016/j.bmcl.2011.01.079
BindingDB Entry DOI: 10.7270/Q2F1901V |
More data for this
Ligand-Target Pair | |
Mitogen-activated protein kinase 10
(Homo sapiens (Human)) | BDBM50340599
(7-(1-methyl-1H-pyrazol-4-yl)-N-(4-(3-morpholino-1H...)Show SMILES Cn1cc(cn1)-c1ccc2cnc(Nc3ccc(cc3)-n3cnc(n3)N3CCOCC3)nc2c1 Show InChI InChI=1S/C24H23N9O/c1-31-15-19(14-27-31)17-2-3-18-13-25-23(29-22(18)12-17)28-20-4-6-21(7-5-20)33-16-26-24(30-33)32-8-10-34-11-9-32/h2-7,12-16H,8-11H2,1H3,(H,25,28,29) | 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 | 90 | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of JNK3 by HRTF |
Bioorg Med Chem Lett 21: 1719-23 (2011)
Article DOI: 10.1016/j.bmcl.2011.01.079
BindingDB Entry DOI: 10.7270/Q2F1901V |
More data for this
Ligand-Target Pair | |
Mitogen-activated protein kinase 10
(Homo sapiens (Human)) | BDBM50340619
((4-(8-(6-methylpyridin-3-yl)quinazolin-2-ylamino)p...)Show SMILES Cc1ccc(cn1)-c1cccc2cnc(Nc3ccc(cc3)C(=O)N3CCOCC3)nc12 Show InChI InChI=1S/C25H23N5O2/c1-17-5-6-19(15-26-17)22-4-2-3-20-16-27-25(29-23(20)22)28-21-9-7-18(8-10-21)24(31)30-11-13-32-14-12-30/h2-10,15-16H,11-14H2,1H3,(H,27,28,29) | 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 | 90 | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of JNK3 by HRTF |
Bioorg Med Chem Lett 21: 1719-23 (2011)
Article DOI: 10.1016/j.bmcl.2011.01.079
BindingDB Entry DOI: 10.7270/Q2F1901V |
More data for this
Ligand-Target Pair | |
Mitogen-activated protein kinase 10
(Homo sapiens (Human)) | BDBM50340615
(8-(3-fluoro-4-methoxyphenyl)-N-(4-(3-(pyridin-2-yl...)Show SMILES COc1ccc(cc1F)-c1cccc2cnc(Nc3ccc(cc3)-n3cnc(n3)-c3ccccn3)nc12 Show InChI InChI=1S/C28H20FN7O/c1-37-25-13-8-18(15-23(25)29)22-6-4-5-19-16-31-28(34-26(19)22)33-20-9-11-21(12-10-20)36-17-32-27(35-36)24-7-2-3-14-30-24/h2-17H,1H3,(H,31,33,34) | 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 | 90 | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of JNK3 by HRTF |
Bioorg Med Chem Lett 21: 1719-23 (2011)
Article DOI: 10.1016/j.bmcl.2011.01.079
BindingDB Entry DOI: 10.7270/Q2F1901V |
More data for this
Ligand-Target Pair | |
Transcription factor Jun
(Homo sapiens (Human)) | BDBM50340622
(8-chloro-7-(1-methyl-1H-pyrazol-4-yl)-N-(4-(3-morp...)Show SMILES Cn1cc(cn1)-c1ccc2cnc(Nc3ccc(cc3)-n3cnc(n3)N3CCOCC3)nc2c1Cl Show InChI InChI=1S/C24H22ClN9O/c1-32-14-17(13-28-32)20-7-2-16-12-26-23(30-22(16)21(20)25)29-18-3-5-19(6-4-18)34-15-27-24(31-34)33-8-10-35-11-9-33/h2-7,12-15H,8-11H2,1H3,(H,26,29,30) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 100 | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of c-Jun |
Bioorg Med Chem Lett 21: 1719-23 (2011)
Article DOI: 10.1016/j.bmcl.2011.01.079
BindingDB Entry DOI: 10.7270/Q2F1901V |
More data for this
Ligand-Target Pair | |
Mitogen-activated protein kinase 8
(Homo sapiens (Human)) | BDBM50340607
(7-(1-methyl-1H-pyrazol-4-yl)-N-(4-(3-(pyridin-2-yl...)Show SMILES Cn1cc(cn1)-c1ccc2cnc(Nc3ccc(cc3)-n3cnc(n3)-c3ccccn3)nc2c1 Show InChI InChI=1S/C25H19N9/c1-33-15-19(14-29-33)17-5-6-18-13-27-25(31-23(18)12-17)30-20-7-9-21(10-8-20)34-16-28-24(32-34)22-4-2-3-11-26-22/h2-16H,1H3,(H,27,30,31) | 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 | 100 | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of JNK1 by HRTF |
Bioorg Med Chem Lett 21: 1719-23 (2011)
Article DOI: 10.1016/j.bmcl.2011.01.079
BindingDB Entry DOI: 10.7270/Q2F1901V |
More data for this
Ligand-Target Pair | |
Transcription factor Jun
(Homo sapiens (Human)) | BDBM50340600
(CHEMBL1761555 | N-(4-(3-morpholino-1H-1,2,4-triazo...)Show SMILES C1CN(CCO1)c1ncn(n1)-c1ccc(Nc2ncc3ccc(cc3n2)-c2cn[nH]c2)cc1 Show InChI InChI=1S/C23H21N9O/c1-2-17-12-24-22(29-21(17)11-16(1)18-13-26-27-14-18)28-19-3-5-20(6-4-19)32-15-25-23(30-32)31-7-9-33-10-8-31/h1-6,11-15H,7-10H2,(H,26,27)(H,24,28,29) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 120 | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of c-Jun |
Bioorg Med Chem Lett 21: 1719-23 (2011)
Article DOI: 10.1016/j.bmcl.2011.01.079
BindingDB Entry DOI: 10.7270/Q2F1901V |
More data for this
Ligand-Target Pair | |
Transcription factor Jun
(Homo sapiens (Human)) | BDBM50340626
(8-cyclopropyl-7-(1-methyl-1H-pyrazol-4-yl)-N-(4-(3...)Show SMILES Cn1cc(cn1)-c1ccc2cnc(Nc3ccc(cc3)-n3cnc(n3)N3CCOCC3)nc2c1C1CC1 Show InChI InChI=1S/C27H27N9O/c1-34-16-20(15-30-34)23-9-4-19-14-28-26(32-25(19)24(23)18-2-3-18)31-21-5-7-22(8-6-21)36-17-29-27(33-36)35-10-12-37-13-11-35/h4-9,14-18H,2-3,10-13H2,1H3,(H,28,31,32) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 130 | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of c-Jun |
Bioorg Med Chem Lett 21: 1719-23 (2011)
Article DOI: 10.1016/j.bmcl.2011.01.079
BindingDB Entry DOI: 10.7270/Q2F1901V |
More data for this
Ligand-Target Pair | |
Transcription factor Jun
(Homo sapiens (Human)) | BDBM50340624
(8-methyl-7-(1-methyl-1H-pyrazol-4-yl)-N-(4-(3-morp...)Show SMILES Cc1c(ccc2cnc(Nc3ccc(cc3)-n3cnc(n3)N3CCOCC3)nc12)-c1cnn(C)c1 Show InChI InChI=1S/C25H25N9O/c1-17-22(19-14-28-32(2)15-19)8-3-18-13-26-24(30-23(17)18)29-20-4-6-21(7-5-20)34-16-27-25(31-34)33-9-11-35-12-10-33/h3-8,13-16H,9-12H2,1-2H3,(H,26,29,30) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 160 | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of c-Jun |
Bioorg Med Chem Lett 21: 1719-23 (2011)
Article DOI: 10.1016/j.bmcl.2011.01.079
BindingDB Entry DOI: 10.7270/Q2F1901V |
More data for this
Ligand-Target Pair | |
Mitogen-activated protein kinase 10
(Homo sapiens (Human)) | BDBM50340618
(CHEMBL1761573 | N-(4-fluorophenyl)-8-(6-methylpyri...)Show InChI InChI=1S/C20H15FN4/c1-13-5-6-14(11-22-13)18-4-2-3-15-12-23-20(25-19(15)18)24-17-9-7-16(21)8-10-17/h2-12H,1H3,(H,23,24,25) | 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 | 170 | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of JNK3 by HRTF |
Bioorg Med Chem Lett 21: 1719-23 (2011)
Article DOI: 10.1016/j.bmcl.2011.01.079
BindingDB Entry DOI: 10.7270/Q2F1901V |
More data for this
Ligand-Target Pair | |
Mitogen-activated protein kinase 10
(Homo sapiens (Human)) | BDBM50340625
(7-(1-methyl-1H-pyrazol-4-yl)-N-(4-(3-morpholino-1H...)Show SMILES Cn1cc(cn1)-c1ccc2cnc(Nc3ccc(cc3)-n3cnc(n3)N3CCOCC3)nc2c1C(F)(F)F Show InChI InChI=1S/C25H22F3N9O/c1-35-14-17(13-31-35)20-7-2-16-12-29-23(33-22(16)21(20)25(26,27)28)32-18-3-5-19(6-4-18)37-15-30-24(34-37)36-8-10-38-11-9-36/h2-7,12-15H,8-11H2,1H3,(H,29,32,33) | 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 | 190 | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of JNK3 by HRTF |
Bioorg Med Chem Lett 21: 1719-23 (2011)
Article DOI: 10.1016/j.bmcl.2011.01.079
BindingDB Entry DOI: 10.7270/Q2F1901V |
More data for this
Ligand-Target Pair | |
Transcription factor Jun
(Homo sapiens (Human)) | BDBM50340614
(CHEMBL1761569 | N-(4-(3-methyl-1H-1,2,4-triazol-1-...)Show SMILES Cc1ncn(n1)-c1ccc(Nc2ncc3cccc(-c4nccs4)c3n2)cc1 Show InChI InChI=1S/C20H15N7S/c1-13-23-12-27(26-13)16-7-5-15(6-8-16)24-20-22-11-14-3-2-4-17(18(14)25-20)19-21-9-10-28-19/h2-12H,1H3,(H,22,24,25) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | 200 | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of c-Jun |
Bioorg Med Chem Lett 21: 1719-23 (2011)
Article DOI: 10.1016/j.bmcl.2011.01.079
BindingDB Entry DOI: 10.7270/Q2F1901V |
More data for this
Ligand-Target Pair | |
Mitogen-activated protein kinase 10
(Homo sapiens (Human)) | BDBM50340603
(CHEMBL1761558 | N-(4-(3-morpholino-1H-1,2,4-triazo...)Show SMILES C1CN(CCO1)c1ncn(n1)-c1ccc(Nc2ncc3ccc(cc3n2)-c2cccnc2)cc1 Show InChI InChI=1S/C25H22N8O/c1-2-19(15-26-9-1)18-3-4-20-16-27-24(30-23(20)14-18)29-21-5-7-22(8-6-21)33-17-28-25(31-33)32-10-12-34-13-11-32/h1-9,14-17H,10-13H2,(H,27,29,30) | 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 | 210 | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of JNK3 by HRTF |
Bioorg Med Chem Lett 21: 1719-23 (2011)
Article DOI: 10.1016/j.bmcl.2011.01.079
BindingDB Entry DOI: 10.7270/Q2F1901V |
More data for this
Ligand-Target Pair | |
Transcription factor Jun
(Homo sapiens (Human)) | BDBM50340610
(8-(3-fluoro-4-methoxyphenyl)-N-(4-(3-morpholino-1H...)Show SMILES COc1ccc(cc1F)-c1cccc2cnc(Nc3ccc(cc3)-n3cnc(n3)N3CCOCC3)nc12 Show InChI InChI=1S/C27H24FN7O2/c1-36-24-10-5-18(15-23(24)28)22-4-2-3-19-16-29-26(32-25(19)22)31-20-6-8-21(9-7-20)35-17-30-27(33-35)34-11-13-37-14-12-34/h2-10,15-17H,11-14H2,1H3,(H,29,31,32) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 250 | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of c-Jun |
Bioorg Med Chem Lett 21: 1719-23 (2011)
Article DOI: 10.1016/j.bmcl.2011.01.079
BindingDB Entry DOI: 10.7270/Q2F1901V |
More data for this
Ligand-Target Pair | |
Transcription factor Jun
(Homo sapiens (Human)) | BDBM50340607
(7-(1-methyl-1H-pyrazol-4-yl)-N-(4-(3-(pyridin-2-yl...)Show SMILES Cn1cc(cn1)-c1ccc2cnc(Nc3ccc(cc3)-n3cnc(n3)-c3ccccn3)nc2c1 Show InChI InChI=1S/C25H19N9/c1-33-15-19(14-29-33)17-5-6-18-13-27-25(31-23(18)12-17)30-20-7-9-21(10-8-20)34-16-28-24(32-34)22-4-2-3-11-26-22/h2-16H,1H3,(H,27,30,31) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | 290 | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of c-Jun |
Bioorg Med Chem Lett 21: 1719-23 (2011)
Article DOI: 10.1016/j.bmcl.2011.01.079
BindingDB Entry DOI: 10.7270/Q2F1901V |
More data for this
Ligand-Target Pair | |
Transcription factor Jun
(Homo sapiens (Human)) | BDBM50340599
(7-(1-methyl-1H-pyrazol-4-yl)-N-(4-(3-morpholino-1H...)Show SMILES Cn1cc(cn1)-c1ccc2cnc(Nc3ccc(cc3)-n3cnc(n3)N3CCOCC3)nc2c1 Show InChI InChI=1S/C24H23N9O/c1-31-15-19(14-27-31)17-2-3-18-13-25-23(29-22(18)12-17)28-20-4-6-21(7-5-20)33-16-26-24(30-33)32-8-10-34-11-9-32/h2-7,12-16H,8-11H2,1H3,(H,25,28,29) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 310 | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of c-Jun |
Bioorg Med Chem Lett 21: 1719-23 (2011)
Article DOI: 10.1016/j.bmcl.2011.01.079
BindingDB Entry DOI: 10.7270/Q2F1901V |
More data for this
Ligand-Target Pair | |
Transcription factor Jun
(Homo sapiens (Human)) | BDBM50340609
(8-(1-methyl-1H-pyrazol-4-yl)-N-(4-(3-morpholino-1H...)Show SMILES Cn1cc(cn1)-c1cccc2cnc(Nc3ccc(cc3)-n3cnc(n3)N3CCOCC3)nc12 Show InChI InChI=1S/C24H23N9O/c1-31-15-18(14-27-31)21-4-2-3-17-13-25-23(29-22(17)21)28-19-5-7-20(8-6-19)33-16-26-24(30-33)32-9-11-34-12-10-32/h2-8,13-16H,9-12H2,1H3,(H,25,28,29) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 330 | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of c-Jun |
Bioorg Med Chem Lett 21: 1719-23 (2011)
Article DOI: 10.1016/j.bmcl.2011.01.079
BindingDB Entry DOI: 10.7270/Q2F1901V |
More data for this
Ligand-Target Pair | |
Transcription factor Jun
(Homo sapiens (Human)) | BDBM50340613
(8-(3-fluoro-4-methoxyphenyl)-N-(4-(3-methyl-1H-1,2...)Show SMILES COc1ccc(cc1F)-c1cccc2cnc(Nc3ccc(cc3)-n3cnc(C)n3)nc12 Show InChI InChI=1S/C24H19FN6O/c1-15-27-14-31(30-15)19-9-7-18(8-10-19)28-24-26-13-17-4-3-5-20(23(17)29-24)16-6-11-22(32-2)21(25)12-16/h3-14H,1-2H3,(H,26,28,29) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 500 | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of c-Jun |
Bioorg Med Chem Lett 21: 1719-23 (2011)
Article DOI: 10.1016/j.bmcl.2011.01.079
BindingDB Entry DOI: 10.7270/Q2F1901V |
More data for this
Ligand-Target Pair | |
Transcription factor Jun
(Homo sapiens (Human)) | BDBM50340623
(8-chloro-7-(1-isopropyl-1H-pyrazol-4-yl)-N-(4-(3-m...)Show SMILES CC(C)n1cc(cn1)-c1ccc2cnc(Nc3ccc(cc3)-n3cnc(n3)N3CCOCC3)nc2c1Cl Show InChI InChI=1S/C26H26ClN9O/c1-17(2)35-15-19(14-30-35)22-8-3-18-13-28-25(32-24(18)23(22)27)31-20-4-6-21(7-5-20)36-16-29-26(33-36)34-9-11-37-12-10-34/h3-8,13-17H,9-12H2,1-2H3,(H,28,31,32) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 620 | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of c-Jun |
Bioorg Med Chem Lett 21: 1719-23 (2011)
Article DOI: 10.1016/j.bmcl.2011.01.079
BindingDB Entry DOI: 10.7270/Q2F1901V |
More data for this
Ligand-Target Pair | |
Transcription factor Jun
(Homo sapiens (Human)) | BDBM50340617
(CHEMBL1761572 | N-(benzo[d][1,3]dioxol-5-yl)-8-(6-...)Show InChI InChI=1S/C21H16N4O2/c1-13-5-6-14(10-22-13)17-4-2-3-15-11-23-21(25-20(15)17)24-16-7-8-18-19(9-16)27-12-26-18/h2-11H,12H2,1H3,(H,23,24,25) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | 630 | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of c-Jun |
Bioorg Med Chem Lett 21: 1719-23 (2011)
Article DOI: 10.1016/j.bmcl.2011.01.079
BindingDB Entry DOI: 10.7270/Q2F1901V |
More data for this
Ligand-Target Pair | |
Mitogen-activated protein kinase 10
(Homo sapiens (Human)) | BDBM50340601
(7-(isoxazol-4-yl)-N-(4-(3-morpholino-1H-1,2,4-tria...)Show SMILES C1CN(CCO1)c1ncn(n1)-c1ccc(Nc2ncc3ccc(cc3n2)-c2cnoc2)cc1 Show InChI InChI=1S/C23H20N8O2/c1-2-17-12-24-22(28-21(17)11-16(1)18-13-26-33-14-18)27-19-3-5-20(6-4-19)31-15-25-23(29-31)30-7-9-32-10-8-30/h1-6,11-15H,7-10H2,(H,24,27,28) | 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 | 700 | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of JNK3 by HRTF |
Bioorg Med Chem Lett 21: 1719-23 (2011)
Article DOI: 10.1016/j.bmcl.2011.01.079
BindingDB Entry DOI: 10.7270/Q2F1901V |
More data for this
Ligand-Target Pair | |
Mitogen-activated protein kinase 10
(Homo sapiens (Human)) | BDBM50340604
(7-(6-methylpyridin-3-yl)-N-(4-(3-morpholino-1H-1,2...)Show SMILES Cc1ccc(cn1)-c1ccc2cnc(Nc3ccc(cc3)-n3cnc(n3)N3CCOCC3)nc2c1 Show InChI InChI=1S/C26H24N8O/c1-18-2-3-20(15-27-18)19-4-5-21-16-28-25(31-24(21)14-19)30-22-6-8-23(9-7-22)34-17-29-26(32-34)33-10-12-35-13-11-33/h2-9,14-17H,10-13H2,1H3,(H,28,30,31) | 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 | 730 | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of JNK3 by HRTF |
Bioorg Med Chem Lett 21: 1719-23 (2011)
Article DOI: 10.1016/j.bmcl.2011.01.079
BindingDB Entry DOI: 10.7270/Q2F1901V |
More data for this
Ligand-Target Pair | |
Transcription factor Jun
(Homo sapiens (Human)) | BDBM50340620
(4-(8-(6-methylpyridin-3-yl)quinazolin-2-ylamino)cy...)Show SMILES Cc1ccc(cn1)-c1cccc2cnc(NC3CCC(O)CC3)nc12 |(-2.41,-16.62,;-3.75,-17.39,;-3.76,-18.93,;-5.09,-19.69,;-6.42,-18.91,;-6.42,-17.38,;-5.08,-16.61,;-7.75,-19.68,;-9.09,-18.9,;-10.42,-19.68,;-10.42,-21.22,;-9.09,-21.99,;-9.11,-23.53,;-7.78,-24.31,;-6.43,-23.55,;-5.1,-24.33,;-3.77,-23.57,;-2.44,-24.35,;-1.11,-23.6,;-1.08,-22.06,;.26,-21.31,;-2.41,-21.28,;-3.76,-22.03,;-6.42,-22,;-7.75,-21.22,)| Show InChI InChI=1S/C20H22N4O/c1-13-5-6-14(11-21-13)18-4-2-3-15-12-22-20(24-19(15)18)23-16-7-9-17(25)10-8-16/h2-6,11-12,16-17,25H,7-10H2,1H3,(H,22,23,24) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | 930 | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of c-Jun |
Bioorg Med Chem Lett 21: 1719-23 (2011)
Article DOI: 10.1016/j.bmcl.2011.01.079
BindingDB Entry DOI: 10.7270/Q2F1901V |
More data for this
Ligand-Target Pair | |
Transcription factor Jun
(Homo sapiens (Human)) | BDBM50340612
(CHEMBL1761567 | N-(4-(3-morpholino-1H-1,2,4-triazo...)Show SMILES C1CN(CCO1)c1ncn(n1)-c1ccc(Nc2ncc3cccc(-c4ccccc4)c3n2)cc1 Show InChI InChI=1S/C26H23N7O/c1-2-5-19(6-3-1)23-8-4-7-20-17-27-25(30-24(20)23)29-21-9-11-22(12-10-21)33-18-28-26(31-33)32-13-15-34-16-14-32/h1-12,17-18H,13-16H2,(H,27,29,30) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| 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 |
The Scripps Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of c-Jun |
Bioorg Med Chem Lett 21: 1719-23 (2011)
Article DOI: 10.1016/j.bmcl.2011.01.079
BindingDB Entry DOI: 10.7270/Q2F1901V |
More data for this
Ligand-Target Pair | |
Transcription factor Jun
(Homo sapiens (Human)) | BDBM50340621
(((cis)-4-(8-(6-methylpyridin-3-yl)quinazolin-2-yla...)Show SMILES Cc1ccc(cn1)-c1cccc2cnc(N[C@H]3CC[C@H](CC3)C(=O)N3CCCC3)nc12 |r,wU:16.16,19.23,(12,-17.01,;10.66,-17.78,;10.65,-19.32,;9.32,-20.08,;7.99,-19.31,;7.99,-17.77,;9.33,-17,;6.66,-20.07,;5.32,-19.29,;3.99,-20.07,;3.99,-21.62,;5.32,-22.38,;5.3,-23.92,;6.64,-24.71,;7.98,-23.94,;9.31,-24.72,;10.65,-23.97,;10.65,-22.42,;12,-21.67,;13.33,-22.46,;13.31,-24,;11.97,-24.75,;14.67,-21.7,;14.69,-20.16,;16,-22.49,;15.98,-24.02,;17.44,-24.52,;18.36,-23.28,;17.47,-22.03,;8,-22.39,;6.66,-21.62,)| Show InChI InChI=1S/C25H29N5O/c1-17-7-8-19(15-26-17)22-6-4-5-20-16-27-25(29-23(20)22)28-21-11-9-18(10-12-21)24(31)30-13-2-3-14-30/h4-8,15-16,18,21H,2-3,9-14H2,1H3,(H,27,28,29)/t18-,21+ | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | 3.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of c-Jun |
Bioorg Med Chem Lett 21: 1719-23 (2011)
Article DOI: 10.1016/j.bmcl.2011.01.079
BindingDB Entry DOI: 10.7270/Q2F1901V |
More data for this
Ligand-Target Pair | |
Transcription factor Jun
(Homo sapiens (Human)) | BDBM50340611
(CHEMBL1761566 | N-(4-(3-morpholino-1H-1,2,4-triazo...)Show SMILES C1CN(CCO1)c1ncn(n1)-c1ccc(Nc2ncc3cccc(-c4nccs4)c3n2)cc1 Show InChI InChI=1S/C23H20N8OS/c1-2-16-14-25-22(28-20(16)19(3-1)21-24-8-13-33-21)27-17-4-6-18(7-5-17)31-15-26-23(29-31)30-9-11-32-12-10-30/h1-8,13-15H,9-12H2,(H,25,27,28) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | 3.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of c-Jun |
Bioorg Med Chem Lett 21: 1719-23 (2011)
Article DOI: 10.1016/j.bmcl.2011.01.079
BindingDB Entry DOI: 10.7270/Q2F1901V |
More data for this
Ligand-Target Pair | |
Mitogen-activated protein kinase 10
(Homo sapiens (Human)) | BDBM50340602
(7-morpholino-N-(4-(3-morpholino-1H-1,2,4-triazol-1...)Show SMILES C1CN(CCO1)c1ncn(n1)-c1ccc(Nc2ncc3ccc(cc3n2)N2CCOCC2)cc1 Show InChI InChI=1S/C24H26N8O2/c1-4-21(30-7-11-33-12-8-30)15-22-18(1)16-25-23(28-22)27-19-2-5-20(6-3-19)32-17-26-24(29-32)31-9-13-34-14-10-31/h1-6,15-17H,7-14H2,(H,25,27,28) | 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 | 4.40E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of JNK3 by HRTF |
Bioorg Med Chem Lett 21: 1719-23 (2011)
Article DOI: 10.1016/j.bmcl.2011.01.079
BindingDB Entry DOI: 10.7270/Q2F1901V |
More data for this
Ligand-Target Pair | |
Transcription factor Jun
(Homo sapiens (Human)) | BDBM50340615
(8-(3-fluoro-4-methoxyphenyl)-N-(4-(3-(pyridin-2-yl...)Show SMILES COc1ccc(cc1F)-c1cccc2cnc(Nc3ccc(cc3)-n3cnc(n3)-c3ccccn3)nc12 Show InChI InChI=1S/C28H20FN7O/c1-37-25-13-8-18(15-23(25)29)22-6-4-5-19-16-31-28(34-26(19)22)33-20-9-11-21(12-10-20)36-17-32-27(35-36)24-7-2-3-14-30-24/h2-17H,1H3,(H,31,33,34) | PDB
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| 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 |
The Scripps Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of c-Jun |
Bioorg Med Chem Lett 21: 1719-23 (2011)
Article DOI: 10.1016/j.bmcl.2011.01.079
BindingDB Entry DOI: 10.7270/Q2F1901V |
More data for this
Ligand-Target Pair | |
Mitogen-activated protein kinase 10
(Homo sapiens (Human)) | BDBM50340605
(CHEMBL1761560 | N-(4-(3-morpholino-1H-1,2,4-triazo...)Show SMILES C1CN(CCO1)c1ncn(n1)-c1ccc(Nc2ncc3ccc(cc3n2)-c2ccccc2)cc1 Show InChI InChI=1S/C26H23N7O/c1-2-4-19(5-3-1)20-6-7-21-17-27-25(30-24(21)16-20)29-22-8-10-23(11-9-22)33-18-28-26(31-33)32-12-14-34-15-13-32/h1-11,16-18H,12-15H2,(H,27,29,30) | 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 | >2.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
The Scripps Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of JNK3 by HRTF |
Bioorg Med Chem Lett 21: 1719-23 (2011)
Article DOI: 10.1016/j.bmcl.2011.01.079
BindingDB Entry DOI: 10.7270/Q2F1901V |
More data for this
Ligand-Target Pair | |
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