Found 317 hits with Last Name = 'cochet' and Initial = 'c' 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 |
|---|
Casein kinase II subunit alpha
(Homo sapiens (Human)) | BDBM50530315
(CHEMBL4520531)Show InChI InChI=1S/C20H14N2O3S/c23-18-10-15(7-8-16(18)19(24)25)21-20-22-17(11-26-20)14-6-5-12-3-1-2-4-13(12)9-14/h1-11,23H,(H,21,22)(H,24,25) | PDB
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| 180 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ de Lyon
Curated by ChEMBL
| Assay Description
Competitive inhibition of recombinant human GST-tagged CK2alpha by Lineweaver-Burk plot analysis |
J Med Chem 62: 1817-1836 (2019)
Article DOI: 10.1021/acs.jmedchem.8b01765
BindingDB Entry DOI: 10.7270/Q2SJ1Q27 |
More data for this
Ligand-Target Pair | 
3D Structure (crystal) |
Casein kinase II subunit alpha
(Homo sapiens (Human)) | BDBM50530315
(CHEMBL4520531)Show InChI InChI=1S/C20H14N2O3S/c23-18-10-15(7-8-16(18)19(24)25)21-20-22-17(11-26-20)14-6-5-12-3-1-2-4-13(12)9-14/h1-11,23H,(H,21,22)(H,24,25) | PDB
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| 180 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ de Lyon
Curated by ChEMBL
| Assay Description
Competitive inhibition of recombinant human GST-tagged CK2alpha by Lineweaver-Burk plot analysis |
J Med Chem 62: 1817-1836 (2019)
Article DOI: 10.1021/acs.jmedchem.8b01765
BindingDB Entry DOI: 10.7270/Q2SJ1Q27 |
More data for this
Ligand-Target Pair |
3D Structure (crystal) |
Casein kinase II subunit alpha
(Homo sapiens (Human)) | BDBM50530325
(CHEMBL4458300)Show InChI InChI=1S/C16H11BrN2O2S/c17-12-3-1-2-11(8-12)14-9-22-16(19-14)18-13-6-4-10(5-7-13)15(20)21/h1-9H,(H,18,19)(H,20,21) | PDB
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| PC cid
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| Article
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| 700 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Saarland University
Curated by ChEMBL
| Assay Description
Mixed-type inhibition of recombinant human GST-tagged CK2alpha in presence of ATP by Lineweaver-Burk plot analysis |
J Med Chem 62: 1803-1816 (2019)
Article DOI: 10.1021/acs.jmedchem.8b01766
BindingDB Entry DOI: 10.7270/Q2NS0ZCZ |
More data for this
Ligand-Target Pair | |
Casein kinase II subunit alpha
(Homo sapiens (Human)) | BDBM50530325
(CHEMBL4458300)Show InChI InChI=1S/C16H11BrN2O2S/c17-12-3-1-2-11(8-12)14-9-22-16(19-14)18-13-6-4-10(5-7-13)15(20)21/h1-9H,(H,18,19)(H,20,21) | PDB
UniProtKB/SwissProt
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| PC cid
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UniChem
| Article
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| 700 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Saarland University
Curated by ChEMBL
| Assay Description
Mixed-type inhibition of recombinant human GST-tagged CK2alpha in presence of ATP by Lineweaver-Burk plot analysis |
J Med Chem 62: 1803-1816 (2019)
Article DOI: 10.1021/acs.jmedchem.8b01766
BindingDB Entry DOI: 10.7270/Q2NS0ZCZ |
More data for this
Ligand-Target Pair | |
Casein kinase II subunit alpha
(Homo sapiens (Human)) | BDBM50530338
(CHEMBL1621959)Show InChI InChI=1S/C16H12N2O2S/c19-15(20)12-6-8-13(9-7-12)17-16-18-14(10-21-16)11-4-2-1-3-5-11/h1-10H,(H,17,18)(H,19,20) | PDB
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| 1.10E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Saarland University
Curated by ChEMBL
| Assay Description
Mixed-type inhibition of recombinant human GST-tagged CK2alpha in presence of ATP by Lineweaver-Burk plot analysis |
J Med Chem 62: 1803-1816 (2019)
Article DOI: 10.1021/acs.jmedchem.8b01766
BindingDB Entry DOI: 10.7270/Q2NS0ZCZ |
More data for this
Ligand-Target Pair |
3D Structure (crystal) |
Casein kinase II subunit alpha
(Homo sapiens (Human)) | BDBM50530338
(CHEMBL1621959)Show InChI InChI=1S/C16H12N2O2S/c19-15(20)12-6-8-13(9-7-12)17-16-18-14(10-21-16)11-4-2-1-3-5-11/h1-10H,(H,17,18)(H,19,20) | PDB
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| 1.10E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Saarland University
Curated by ChEMBL
| Assay Description
Mixed-type inhibition of recombinant human GST-tagged CK2alpha in presence of ATP by Lineweaver-Burk plot analysis |
J Med Chem 62: 1803-1816 (2019)
Article DOI: 10.1021/acs.jmedchem.8b01766
BindingDB Entry DOI: 10.7270/Q2NS0ZCZ |
More data for this
Ligand-Target Pair |
3D Structure (crystal) |
Casein kinase II subunit alpha
(Homo sapiens (Human)) | BDBM50530336
(CHEMBL4462082)Show SMILES OC(=O)c1ccc(Nc2nc(cs2)-c2cccc(c2)[N+]([O-])=O)cc1 Show InChI InChI=1S/C16H11N3O4S/c20-15(21)10-4-6-12(7-5-10)17-16-18-14(9-24-16)11-2-1-3-13(8-11)19(22)23/h1-9H,(H,17,18)(H,20,21) | PDB
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| 1.60E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Saarland University
Curated by ChEMBL
| Assay Description
Mixed-type inhibition of recombinant human GST-tagged CK2alpha in presence of ATP by Lineweaver-Burk plot analysis |
J Med Chem 62: 1803-1816 (2019)
Article DOI: 10.1021/acs.jmedchem.8b01766
BindingDB Entry DOI: 10.7270/Q2NS0ZCZ |
More data for this
Ligand-Target Pair | |
Casein kinase II subunit alpha
(Homo sapiens (Human)) | BDBM50530336
(CHEMBL4462082)Show SMILES OC(=O)c1ccc(Nc2nc(cs2)-c2cccc(c2)[N+]([O-])=O)cc1 Show InChI InChI=1S/C16H11N3O4S/c20-15(21)10-4-6-12(7-5-10)17-16-18-14(9-24-16)11-2-1-3-13(8-11)19(22)23/h1-9H,(H,17,18)(H,20,21) | PDB
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| 1.60E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Saarland University
Curated by ChEMBL
| Assay Description
Mixed-type inhibition of recombinant human GST-tagged CK2alpha in presence of ATP by Lineweaver-Burk plot analysis |
J Med Chem 62: 1803-1816 (2019)
Article DOI: 10.1021/acs.jmedchem.8b01766
BindingDB Entry DOI: 10.7270/Q2NS0ZCZ |
More data for this
Ligand-Target Pair | |
Dual specificity protein kinase CLK2
(Homo sapiens (Human)) | BDBM50335638
(5-(3-Chlorophenylamino)benzo[c][2,6]naphthyridine-...)Show SMILES OC(=O)c1ccc2c(c1)nc(Nc1cccc(Cl)c1)c1ccncc21 Show InChI InChI=1S/C19H12ClN3O2/c20-12-2-1-3-13(9-12)22-18-15-6-7-21-10-16(15)14-5-4-11(19(24)25)8-17(14)23-18/h1-10H,(H,22,23)(H,24,25) | PDB
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Universit£ de Lyon
Curated by ChEMBL
| Assay Description
Inhibition of N-terminal GST-tagged human CLK2 (138 to end residues) using SR-rich substrate and [gamma-33P]ATP incubated for 40 mins by scintillatio... |
J Med Chem 62: 1817-1836 (2019)
Article DOI: 10.1021/acs.jmedchem.8b01765
BindingDB Entry DOI: 10.7270/Q2SJ1Q27 |
More data for this
Ligand-Target Pair |
3D Structure (crystal) |
Dual specificity protein kinase CLK2
(Homo sapiens (Human)) | BDBM50335638
(5-(3-Chlorophenylamino)benzo[c][2,6]naphthyridine-...)Show SMILES OC(=O)c1ccc2c(c1)nc(Nc1cccc(Cl)c1)c1ccncc21 Show InChI InChI=1S/C19H12ClN3O2/c20-12-2-1-3-13(9-12)22-18-15-6-7-21-10-16(15)14-5-4-11(19(24)25)8-17(14)23-18/h1-10H,(H,22,23)(H,24,25) | PDB
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| n/a | n/a | 4 | n/a | n/a | n/a | n/a | n/a | n/a |
Saarland University
Curated by ChEMBL
| Assay Description
Inhibition of recombinant human CLK2 in presence of ATP by radiometric filter-binding assay |
J Med Chem 62: 1803-1816 (2019)
Article DOI: 10.1021/acs.jmedchem.8b01766
BindingDB Entry DOI: 10.7270/Q2NS0ZCZ |
More data for this
Ligand-Target Pair |
3D Structure (crystal) |
Dual specificity protein kinase CLK2
(Homo sapiens (Human)) | BDBM50335638
(5-(3-Chlorophenylamino)benzo[c][2,6]naphthyridine-...)Show SMILES OC(=O)c1ccc2c(c1)nc(Nc1cccc(Cl)c1)c1ccncc21 Show InChI InChI=1S/C19H12ClN3O2/c20-12-2-1-3-13(9-12)22-18-15-6-7-21-10-16(15)14-5-4-11(19(24)25)8-17(14)23-18/h1-10H,(H,22,23)(H,24,25) | PDB
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Saarland University
Curated by ChEMBL
| Assay Description
Inhibition of recombinant human CLK2 in presence of ATP by radiometric filter-binding assay |
J Med Chem 62: 1803-1816 (2019)
Article DOI: 10.1021/acs.jmedchem.8b01766
BindingDB Entry DOI: 10.7270/Q2NS0ZCZ |
More data for this
Ligand-Target Pair |
3D Structure (crystal) |
Dual specificity protein kinase CLK2
(Homo sapiens (Human)) | BDBM50335638
(5-(3-Chlorophenylamino)benzo[c][2,6]naphthyridine-...)Show SMILES OC(=O)c1ccc2c(c1)nc(Nc1cccc(Cl)c1)c1ccncc21 Show InChI InChI=1S/C19H12ClN3O2/c20-12-2-1-3-13(9-12)22-18-15-6-7-21-10-16(15)14-5-4-11(19(24)25)8-17(14)23-18/h1-10H,(H,22,23)(H,24,25) | PDB
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Universit£ de Lyon
Curated by ChEMBL
| Assay Description
Inhibition of N-terminal GST-tagged human CLK2 (138 to end residues) using SR-rich substrate and [gamma-33P]ATP incubated for 40 mins by scintillatio... |
J Med Chem 62: 1817-1836 (2019)
Article DOI: 10.1021/acs.jmedchem.8b01765
BindingDB Entry DOI: 10.7270/Q2SJ1Q27 |
More data for this
Ligand-Target Pair |
3D Structure (crystal) |
Casein kinase II subunit alpha
(Homo sapiens (Human)) | BDBM616483
(US20230278983, Code AB1455)Show SMILES COc1cccc(CO)c1-c1ccc(cc1C)S(=O)(=O)NCCN1CCC(Cn2cc(nn2)-c2c([nH]c3ccc(F)cc23)C(C)=O)CC1 |(-8.41,5.78,;-7.01,6.41,;-6.85,7.94,;-8.09,8.85,;-7.93,10.38,;-6.52,11,;-5.28,10.1,;-3.87,10.72,;-2.62,9.82,;-5.44,8.57,;-4.19,7.66,;-2.79,8.29,;-1.54,7.38,;-1.7,5.85,;-3.11,5.22,;-4.35,6.13,;-5.76,5.5,;-.46,4.95,;.45,6.19,;-1.36,3.7,;.79,4.04,;.63,2.51,;1.88,1.6,;1.71,.07,;.31,-.55,;.15,-2.09,;1.39,-2.99,;1.23,-4.52,;2.48,-5.43,;2.48,-6.97,;3.94,-7.44,;4.85,-6.2,;3.94,-4.95,;4.42,-8.91,;3.51,-10.15,;4.42,-11.4,;5.88,-10.92,;7.22,-11.69,;8.55,-10.92,;8.55,-9.38,;9.88,-8.61,;7.22,-8.61,;5.88,-9.38,;1.97,-10.15,;1.2,-8.82,;1.2,-11.49,;2.8,-2.36,;2.96,-.83,)| | PDB
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TBA
| |
Citation and Details
BindingDB Entry DOI: 10.7270/Q2WH2V4R |
More data for this
Ligand-Target Pair | |
Dual specificity tyrosine-phosphorylation-regulated kinase 1B
(Homo sapiens (Human)) | BDBM50335638
(5-(3-Chlorophenylamino)benzo[c][2,6]naphthyridine-...)Show SMILES OC(=O)c1ccc2c(c1)nc(Nc1cccc(Cl)c1)c1ccncc21 Show InChI InChI=1S/C19H12ClN3O2/c20-12-2-1-3-13(9-12)22-18-15-6-7-21-10-16(15)14-5-4-11(19(24)25)8-17(14)23-18/h1-10H,(H,22,23)(H,24,25) | PDB
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| n/a | n/a | 6.40 | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ de Lyon
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant DyrK1b by fluorescence-based immunoassay |
J Med Chem 62: 1817-1836 (2019)
Article DOI: 10.1021/acs.jmedchem.8b01765
BindingDB Entry DOI: 10.7270/Q2SJ1Q27 |
More data for this
Ligand-Target Pair | |
Dual specificity tyrosine-phosphorylation-regulated kinase 1B
(Homo sapiens (Human)) | BDBM50335638
(5-(3-Chlorophenylamino)benzo[c][2,6]naphthyridine-...)Show SMILES OC(=O)c1ccc2c(c1)nc(Nc1cccc(Cl)c1)c1ccncc21 Show InChI InChI=1S/C19H12ClN3O2/c20-12-2-1-3-13(9-12)22-18-15-6-7-21-10-16(15)14-5-4-11(19(24)25)8-17(14)23-18/h1-10H,(H,22,23)(H,24,25) | PDB
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| n/a | n/a | 6.40 | n/a | n/a | n/a | n/a | n/a | n/a |
Saarland University
Curated by ChEMBL
| Assay Description
Inhibition of recombinant human DYRK1B in presence of ATP by radiometric filter-binding assay |
J Med Chem 62: 1803-1816 (2019)
Article DOI: 10.1021/acs.jmedchem.8b01766
BindingDB Entry DOI: 10.7270/Q2NS0ZCZ |
More data for this
Ligand-Target Pair | |
Dual specificity tyrosine-phosphorylation-regulated kinase 1B
(Homo sapiens (Human)) | BDBM50335638
(5-(3-Chlorophenylamino)benzo[c][2,6]naphthyridine-...)Show SMILES OC(=O)c1ccc2c(c1)nc(Nc1cccc(Cl)c1)c1ccncc21 Show InChI InChI=1S/C19H12ClN3O2/c20-12-2-1-3-13(9-12)22-18-15-6-7-21-10-16(15)14-5-4-11(19(24)25)8-17(14)23-18/h1-10H,(H,22,23)(H,24,25) | PDB
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Universit£ de Lyon
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant DyrK1b by fluorescence-based immunoassay |
J Med Chem 62: 1817-1836 (2019)
Article DOI: 10.1021/acs.jmedchem.8b01765
BindingDB Entry DOI: 10.7270/Q2SJ1Q27 |
More data for this
Ligand-Target Pair | |
Dual specificity tyrosine-phosphorylation-regulated kinase 1B
(Homo sapiens (Human)) | BDBM50335638
(5-(3-Chlorophenylamino)benzo[c][2,6]naphthyridine-...)Show SMILES OC(=O)c1ccc2c(c1)nc(Nc1cccc(Cl)c1)c1ccncc21 Show InChI InChI=1S/C19H12ClN3O2/c20-12-2-1-3-13(9-12)22-18-15-6-7-21-10-16(15)14-5-4-11(19(24)25)8-17(14)23-18/h1-10H,(H,22,23)(H,24,25) | PDB
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Saarland University
Curated by ChEMBL
| Assay Description
Inhibition of recombinant human DYRK1B in presence of ATP by radiometric filter-binding assay |
J Med Chem 62: 1803-1816 (2019)
Article DOI: 10.1021/acs.jmedchem.8b01766
BindingDB Entry DOI: 10.7270/Q2NS0ZCZ |
More data for this
Ligand-Target Pair | |
Dual specificity tyrosine-phosphorylation-regulated kinase 1A
(Homo sapiens (Human)) | BDBM50335638
(5-(3-Chlorophenylamino)benzo[c][2,6]naphthyridine-...)Show SMILES OC(=O)c1ccc2c(c1)nc(Nc1cccc(Cl)c1)c1ccncc21 Show InChI InChI=1S/C19H12ClN3O2/c20-12-2-1-3-13(9-12)22-18-15-6-7-21-10-16(15)14-5-4-11(19(24)25)8-17(14)23-18/h1-10H,(H,22,23)(H,24,25) | PDB
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Universit£ de Lyon
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant DyrK1a by fluorescence-based immunoassay |
J Med Chem 62: 1817-1836 (2019)
Article DOI: 10.1021/acs.jmedchem.8b01765
BindingDB Entry DOI: 10.7270/Q2SJ1Q27 |
More data for this
Ligand-Target Pair |
3D Structure (crystal) |
Dual specificity tyrosine-phosphorylation-regulated kinase 1A
(Homo sapiens (Human)) | BDBM50335638
(5-(3-Chlorophenylamino)benzo[c][2,6]naphthyridine-...)Show SMILES OC(=O)c1ccc2c(c1)nc(Nc1cccc(Cl)c1)c1ccncc21 Show InChI InChI=1S/C19H12ClN3O2/c20-12-2-1-3-13(9-12)22-18-15-6-7-21-10-16(15)14-5-4-11(19(24)25)8-17(14)23-18/h1-10H,(H,22,23)(H,24,25) | PDB
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| n/a | n/a | 6.80 | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ de Lyon
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant DyrK1a by fluorescence-based immunoassay |
J Med Chem 62: 1817-1836 (2019)
Article DOI: 10.1021/acs.jmedchem.8b01765
BindingDB Entry DOI: 10.7270/Q2SJ1Q27 |
More data for this
Ligand-Target Pair |
3D Structure (crystal) |
Dual specificity tyrosine-phosphorylation-regulated kinase 1A
(Homo sapiens (Human)) | BDBM50335638
(5-(3-Chlorophenylamino)benzo[c][2,6]naphthyridine-...)Show SMILES OC(=O)c1ccc2c(c1)nc(Nc1cccc(Cl)c1)c1ccncc21 Show InChI InChI=1S/C19H12ClN3O2/c20-12-2-1-3-13(9-12)22-18-15-6-7-21-10-16(15)14-5-4-11(19(24)25)8-17(14)23-18/h1-10H,(H,22,23)(H,24,25) | PDB
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Saarland University
Curated by ChEMBL
| Assay Description
Inhibition of recombinant human DYRK1A in presence of ATP by radiometric filter-binding assay |
J Med Chem 62: 1803-1816 (2019)
Article DOI: 10.1021/acs.jmedchem.8b01766
BindingDB Entry DOI: 10.7270/Q2NS0ZCZ |
More data for this
Ligand-Target Pair |
3D Structure (crystal) |
Dual specificity tyrosine-phosphorylation-regulated kinase 1A
(Homo sapiens (Human)) | BDBM50335638
(5-(3-Chlorophenylamino)benzo[c][2,6]naphthyridine-...)Show SMILES OC(=O)c1ccc2c(c1)nc(Nc1cccc(Cl)c1)c1ccncc21 Show InChI InChI=1S/C19H12ClN3O2/c20-12-2-1-3-13(9-12)22-18-15-6-7-21-10-16(15)14-5-4-11(19(24)25)8-17(14)23-18/h1-10H,(H,22,23)(H,24,25) | PDB
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Saarland University
Curated by ChEMBL
| Assay Description
Inhibition of recombinant human DYRK1A in presence of ATP by radiometric filter-binding assay |
J Med Chem 62: 1803-1816 (2019)
Article DOI: 10.1021/acs.jmedchem.8b01766
BindingDB Entry DOI: 10.7270/Q2NS0ZCZ |
More data for this
Ligand-Target Pair |
3D Structure (crystal) |
Dual specificity tyrosine-phosphorylation-regulated kinase 1A
(RAT) | BDBM50347750
(CHEMBL1802358)Show SMILES O=C1NC(Nc2ccccc2)=NC1=Cc1ccc2OCOc2c1 |w:13.15,c:11| Show InChI InChI=1S/C17H13N3O3/c21-16-13(8-11-6-7-14-15(9-11)23-10-22-14)19-17(20-16)18-12-4-2-1-3-5-12/h1-9H,10H2,(H2,18,19,20,21) | PDB
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CNRS
Curated by ChEMBL
| Assay Description
Inhibition of rat DYRK1A isolated from brain using KKISGRLSPIMTEQ as substrate and [gamma33P]ATP after 30 mins by scintillation counting |
J Med Chem 55: 9312-30 (2012)
Article DOI: 10.1021/jm301034u
BindingDB Entry DOI: 10.7270/Q2571D55 |
More data for this
Ligand-Target Pair | |
Casein kinase II subunit alpha
(Homo sapiens (Human)) | BDBM616482
(US20230278983, Code AB1454)Show SMILES COc1cccc(CO)c1-c1ccc(cc1F)S(=O)(=O)NCCN1CCC(Cn2cc(nn2)-c2c([nH]c3ccc(F)cc23)C(C)=O)CC1 |(-8.41,5.78,;-7.01,6.41,;-6.85,7.94,;-8.09,8.85,;-7.93,10.38,;-6.52,11,;-5.28,10.1,;-3.87,10.72,;-2.62,9.82,;-5.44,8.57,;-4.19,7.66,;-2.79,8.29,;-1.54,7.38,;-1.7,5.85,;-3.11,5.22,;-4.35,6.13,;-5.76,5.5,;-.46,4.95,;.45,6.19,;-1.36,3.7,;.79,4.04,;.63,2.51,;1.88,1.6,;1.71,.07,;.31,-.55,;.15,-2.09,;1.39,-2.99,;1.23,-4.52,;2.48,-5.43,;2.48,-6.97,;3.94,-7.44,;4.85,-6.2,;3.94,-4.95,;4.42,-8.91,;3.51,-10.15,;4.42,-11.4,;5.88,-10.92,;7.22,-11.69,;8.55,-10.92,;8.55,-9.38,;9.88,-8.61,;7.22,-8.61,;5.88,-9.38,;1.97,-10.15,;1.2,-8.82,;1.2,-11.49,;2.8,-2.36,;2.96,-.83,)| | PDB
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TBA
| |
Citation and Details
BindingDB Entry DOI: 10.7270/Q2WH2V4R |
More data for this
Ligand-Target Pair | |
Casein kinase II subunit alpha
(Homo sapiens (Human)) | BDBM165207
(US8168651, Compound TABLE 16.1 | US9062043, Table ...)Show InChI InChI=1S/C19H13N3O2/c23-19(24)12-6-7-14-16-11-20-9-8-15(16)18(22-17(14)10-12)21-13-4-2-1-3-5-13/h1-11H,(H,21,22)(H,23,24) | PDB
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Saarland University
Curated by ChEMBL
| Assay Description
Inhibition of recombinant human GST-tagged CK2alpha in presence of ATP by radiometric filter-binding assay |
J Med Chem 62: 1803-1816 (2019)
Article DOI: 10.1021/acs.jmedchem.8b01766
BindingDB Entry DOI: 10.7270/Q2NS0ZCZ |
More data for this
Ligand-Target Pair | |
Casein kinase II subunit alpha
(Homo sapiens (Human)) | BDBM50335638
(5-(3-Chlorophenylamino)benzo[c][2,6]naphthyridine-...)Show SMILES OC(=O)c1ccc2c(c1)nc(Nc1cccc(Cl)c1)c1ccncc21 Show InChI InChI=1S/C19H12ClN3O2/c20-12-2-1-3-13(9-12)22-18-15-6-7-21-10-16(15)14-5-4-11(19(24)25)8-17(14)23-18/h1-10H,(H,22,23)(H,24,25) | PDB
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Universit£ de Lyon
Curated by ChEMBL
| Assay Description
Inhibition of recombinant human CK2alpha using RRRDDDSDDD substrate and [gamma-33P]ATP by scintillation counting method |
J Med Chem 62: 1817-1836 (2019)
Article DOI: 10.1021/acs.jmedchem.8b01765
BindingDB Entry DOI: 10.7270/Q2SJ1Q27 |
More data for this
Ligand-Target Pair |
3D Structure (crystal) |
Casein kinase II subunit alpha
(Homo sapiens (Human)) | BDBM50335638
(5-(3-Chlorophenylamino)benzo[c][2,6]naphthyridine-...)Show SMILES OC(=O)c1ccc2c(c1)nc(Nc1cccc(Cl)c1)c1ccncc21 Show InChI InChI=1S/C19H12ClN3O2/c20-12-2-1-3-13(9-12)22-18-15-6-7-21-10-16(15)14-5-4-11(19(24)25)8-17(14)23-18/h1-10H,(H,22,23)(H,24,25) | PDB
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Universit£ de Lyon
Curated by ChEMBL
| Assay Description
Inhibition of recombinant human CK2alpha using RRRDDDSDDD substrate and [gamma-33P]ATP by scintillation counting method |
J Med Chem 62: 1817-1836 (2019)
Article DOI: 10.1021/acs.jmedchem.8b01765
BindingDB Entry DOI: 10.7270/Q2SJ1Q27 |
More data for this
Ligand-Target Pair |
3D Structure (crystal) |
Casein kinase II subunit alpha
(Homo sapiens (Human)) | BDBM165207
(US8168651, Compound TABLE 16.1 | US9062043, Table ...)Show InChI InChI=1S/C19H13N3O2/c23-19(24)12-6-7-14-16-11-20-9-8-15(16)18(22-17(14)10-12)21-13-4-2-1-3-5-13/h1-11H,(H,21,22)(H,23,24) | PDB
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Saarland University
Curated by ChEMBL
| Assay Description
Inhibition of recombinant human GST-tagged CK2alpha in presence of ATP by radiometric filter-binding assay |
J Med Chem 62: 1803-1816 (2019)
Article DOI: 10.1021/acs.jmedchem.8b01766
BindingDB Entry DOI: 10.7270/Q2NS0ZCZ |
More data for this
Ligand-Target Pair | |
Casein kinase II subunit alpha
(Homo sapiens (Human)) | BDBM50335638
(5-(3-Chlorophenylamino)benzo[c][2,6]naphthyridine-...)Show SMILES OC(=O)c1ccc2c(c1)nc(Nc1cccc(Cl)c1)c1ccncc21 Show InChI InChI=1S/C19H12ClN3O2/c20-12-2-1-3-13(9-12)22-18-15-6-7-21-10-16(15)14-5-4-11(19(24)25)8-17(14)23-18/h1-10H,(H,22,23)(H,24,25) | PDB
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Universit£ de Lyon
Curated by ChEMBL
| Assay Description
Inhibition of recombinant human GST-tagged CK2alpha in presence of ATP by radiometric kinase assay |
J Med Chem 62: 1817-1836 (2019)
Article DOI: 10.1021/acs.jmedchem.8b01765
BindingDB Entry DOI: 10.7270/Q2SJ1Q27 |
More data for this
Ligand-Target Pair |
3D Structure (crystal) |
Casein kinase II subunit alpha
(Homo sapiens (Human)) | BDBM50335638
(5-(3-Chlorophenylamino)benzo[c][2,6]naphthyridine-...)Show SMILES OC(=O)c1ccc2c(c1)nc(Nc1cccc(Cl)c1)c1ccncc21 Show InChI InChI=1S/C19H12ClN3O2/c20-12-2-1-3-13(9-12)22-18-15-6-7-21-10-16(15)14-5-4-11(19(24)25)8-17(14)23-18/h1-10H,(H,22,23)(H,24,25) | PDB
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Universit£ de Lyon
Curated by ChEMBL
| Assay Description
Inhibition of recombinant human GST-tagged CK2alpha in presence of ATP by radiometric kinase assay |
J Med Chem 62: 1817-1836 (2019)
Article DOI: 10.1021/acs.jmedchem.8b01765
BindingDB Entry DOI: 10.7270/Q2SJ1Q27 |
More data for this
Ligand-Target Pair |
3D Structure (crystal) |
Casein kinase II subunit alpha
(Homo sapiens (Human)) | BDBM616454
(US20230278983, Code AB1206)Show SMILES COc1cccc(CO)c1-c1ccc(cc1)S(=O)(=O)NCCN1CCC(Cn2cc(nn2)-c2c([nH]c3ccc(F)cc23)C(=O)OCC(C)C)CC1 | PDB
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TBA
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Citation and Details
BindingDB Entry DOI: 10.7270/Q2WH2V4R |
More data for this
Ligand-Target Pair | |
Casein kinase II subunit alpha
(Homo sapiens (Human)) | BDBM50132260
(2-(2-Chloro-4-iodo-phenylamino)-N-cyclopropylmetho...)Show InChI InChI=1S/C17H14ClF2IN2O2/c18-12-7-10(21)3-6-14(12)22-16-11(4-5-13(19)15(16)20)17(24)23-25-8-9-1-2-9/h3-7,9,22H,1-2,8H2,(H,23,24) | PDB
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Universit£ de Lyon
Curated by ChEMBL
| Assay Description
Inhibition of recombinant human GST-tagged CK2alpha in presence of ATP by radiometric kinase assay |
J Med Chem 62: 1817-1836 (2019)
Article DOI: 10.1021/acs.jmedchem.8b01765
BindingDB Entry DOI: 10.7270/Q2SJ1Q27 |
More data for this
Ligand-Target Pair | |
Casein kinase II subunit alpha
(Homo sapiens (Human)) | BDBM616473
(US20230278983, Code AB1381)Show SMILES CC(=O)c1[nH]c2ccc(F)cc2c1-c1cn(CC2CCN(CCNS(=O)(=O)c3ccc(cc3)-c3c(O)cccc3F)CC2)nn1 | PDB
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TBA
| |
Citation and Details
BindingDB Entry DOI: 10.7270/Q2WH2V4R |
More data for this
Ligand-Target Pair | |
Casein kinase II subunit alpha
(Homo sapiens (Human)) | BDBM50132260
(2-(2-Chloro-4-iodo-phenylamino)-N-cyclopropylmetho...)Show InChI InChI=1S/C17H14ClF2IN2O2/c18-12-7-10(21)3-6-14(12)22-16-11(4-5-13(19)15(16)20)17(24)23-25-8-9-1-2-9/h3-7,9,22H,1-2,8H2,(H,23,24) | PDB
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Universit£ de Lyon
Curated by ChEMBL
| Assay Description
Inhibition of recombinant human GST-tagged CK2alpha in presence of ATP by radiometric kinase assay |
J Med Chem 62: 1817-1836 (2019)
Article DOI: 10.1021/acs.jmedchem.8b01765
BindingDB Entry DOI: 10.7270/Q2SJ1Q27 |
More data for this
Ligand-Target Pair | |
Casein kinase II subunit alpha
(Homo sapiens (Human)) | BDBM616446
(US20230278983, Code AB1073)Show SMILES CC(C)COC(=O)c1[nH]c2ccc(F)cc2c1-c1cn(CC2CCN(CCNS(=O)(=O)c3ccc(cc3)-c3cccnc3N3CCCC3)CC2)nn1 | PDB
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TBA
| |
Citation and Details
BindingDB Entry DOI: 10.7270/Q2WH2V4R |
More data for this
Ligand-Target Pair | |
Casein kinase II subunit alpha
(Homo sapiens (Human)) | BDBM616474
(US20230278983, Code AB1394)Show SMILES CC(=O)c1[nH]c2ccc(F)cc2c1-c1cn(CC2CCN(CCNS(=O)(=O)c3ccc(cc3)-c3ccccc3C(F)(F)F)CC2)nn1 | PDB
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Citation and Details
BindingDB Entry DOI: 10.7270/Q2WH2V4R |
More data for this
Ligand-Target Pair | |
Casein kinase II subunit alpha
(Homo sapiens (Human)) | BDBM616451
(US20230278983, Code AB1133)Show SMILES CC(C)COC(=O)c1[nH]c2ccc(F)cc2c1-c1cn(CC2CCN(CCNS(=O)(=O)c3ccc(cc3)-c3cccnc3Cl)CC2)nn1 | PDB
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TBA
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Citation and Details
BindingDB Entry DOI: 10.7270/Q2WH2V4R |
More data for this
Ligand-Target Pair | |
Dual specificity tyrosine-phosphorylation-regulated kinase 1B
(Homo sapiens (Human)) | BDBM100152
(7-methoxy-1-methyl-9H-beta-carboline;hydrochloride...)Show InChI InChI=1S/C13H12N2O/c1-8-13-11(5-6-14-8)10-4-3-9(16-2)7-12(10)15-13/h3-7,15H,1-2H3 | PDB
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CNRS
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant GST-tagged DYRK1B expressed in Escherichia coli using GRSRSRSRSRSR as substrate and [gamma33P]ATP after 30 mins by sc... |
J Med Chem 55: 9312-30 (2012)
Article DOI: 10.1021/jm301034u
BindingDB Entry DOI: 10.7270/Q2571D55 |
More data for this
Ligand-Target Pair | |
Casein kinase II subunit alpha
(Homo sapiens (Human)) | BDBM616466
(US20230278983, Code AB1303)Show SMILES COCc1ccccc1-c1ccc(cc1)S(=O)(=O)NCCN1CCC(Cn2cc(nn2)-c2c([nH]c3ccc(F)cc23)C(=O)OCC(C)C)CC1 | PDB
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TBA
| |
Citation and Details
BindingDB Entry DOI: 10.7270/Q2WH2V4R |
More data for this
Ligand-Target Pair | |
Dual specificity tyrosine-phosphorylation-regulated kinase 1A
(RAT) | BDBM100152
(7-methoxy-1-methyl-9H-beta-carboline;hydrochloride...)Show InChI InChI=1S/C13H12N2O/c1-8-13-11(5-6-14-8)10-4-3-9(16-2)7-12(10)15-13/h3-7,15H,1-2H3 | PDB
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CNRS
Curated by ChEMBL
| Assay Description
Inhibition of rat DYRK1A isolated from brain using KKISGRLSPIMTEQ as substrate and [gamma33P]ATP after 30 mins by scintillation counting |
J Med Chem 55: 9312-30 (2012)
Article DOI: 10.1021/jm301034u
BindingDB Entry DOI: 10.7270/Q2571D55 |
More data for this
Ligand-Target Pair |
3D Structure (crystal) |
Dual specificity tyrosine-phosphorylation-regulated kinase 1A
(RAT) | BDBM50347750
(CHEMBL1802358)Show SMILES O=C1NC(Nc2ccccc2)=NC1=Cc1ccc2OCOc2c1 |w:13.15,c:11| Show InChI InChI=1S/C17H13N3O3/c21-16-13(8-11-6-7-14-15(9-11)23-10-22-14)19-17(20-16)18-12-4-2-1-3-5-12/h1-9H,10H2,(H2,18,19,20,21) | PDB
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CNRS
Curated by ChEMBL
| Assay Description
Inhibition of rat recombinant C-terminal truncated GST-tagged DYRK1A expressed in Escherichia coli using GRSRSRSRSRSR as substrate and [gamma33P]ATP ... |
J Med Chem 55: 9312-30 (2012)
Article DOI: 10.1021/jm301034u
BindingDB Entry DOI: 10.7270/Q2571D55 |
More data for this
Ligand-Target Pair | |
Casein kinase II subunit alpha
(Homo sapiens (Human)) | BDBM616423
(US20230278983, Code AB668)Show SMILES CC(C)COC(=O)c1[nH]c2ccc(F)cc2c1-c1cn(CC2CCN(CCNS(=O)(=O)c3ccc(CC(C)C)cc3)CC2)nn1 | PDB
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TBA
| |
Citation and Details
BindingDB Entry DOI: 10.7270/Q2WH2V4R |
More data for this
Ligand-Target Pair |
3D Structure (crystal) |
Dual specificity tyrosine-phosphorylation-regulated kinase 1B
(Homo sapiens (Human)) | BDBM50347750
(CHEMBL1802358)Show SMILES O=C1NC(Nc2ccccc2)=NC1=Cc1ccc2OCOc2c1 |w:13.15,c:11| Show InChI InChI=1S/C17H13N3O3/c21-16-13(8-11-6-7-14-15(9-11)23-10-22-14)19-17(20-16)18-12-4-2-1-3-5-12/h1-9H,10H2,(H2,18,19,20,21) | PDB
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CNRS
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant GST-tagged DYRK1B expressed in Escherichia coli using GRSRSRSRSRSR as substrate and [gamma33P]ATP after 30 mins by sc... |
J Med Chem 55: 9312-30 (2012)
Article DOI: 10.1021/jm301034u
BindingDB Entry DOI: 10.7270/Q2571D55 |
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Ligand-Target Pair | |
Casein kinase II subunit alpha
(Homo sapiens (Human)) | BDBM616476
(US20230278983, Code AB1402)Show SMILES CC(C)COC(=O)c1[nH]c2ccc(F)cc2c1-c1cn(CC2CCN(CCNS(=O)(=O)c3ccc(cc3)-c3c(O)cccc3C(F)(F)F)CC2)nn1 | PDB
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TBA
| |
Citation and Details
BindingDB Entry DOI: 10.7270/Q2WH2V4R |
More data for this
Ligand-Target Pair | |
Casein kinase II subunit alpha
(Homo sapiens (Human)) | BDBM616455
(US20230278983, Code AB1208)Show SMILES CC(C)COC(=O)c1[nH]c2ccc(F)cc2c1-c1cn(CC2CCN(CCNS(=O)(=O)c3ccc(cc3)-c3c(F)cccc3F)CC2)nn1 | PDB
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TBA
| |
Citation and Details
BindingDB Entry DOI: 10.7270/Q2WH2V4R |
More data for this
Ligand-Target Pair | |
Casein kinase II subunit alpha
(Homo sapiens (Human)) | BDBM616481
(US20230278983, Code AB1451)Show SMILES CC(=O)c1[nH]c2ccc(F)cc2c1-c1cn(CC2CCN(CCNS(=O)(=O)c3ccc(cc3)-c3c(F)cccc3C(F)(F)F)CC2)nn1 | PDB
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TBA
| |
Citation and Details
BindingDB Entry DOI: 10.7270/Q2WH2V4R |
More data for this
Ligand-Target Pair | |
Casein kinase II subunit alpha
(Homo sapiens (Human)) | BDBM616449
(US20230278983, Code AB1076)Show SMILES CC(C)COC(=O)c1[nH]c2ccc(F)cc2c1-c1cn(CC2CCN(CCNS(=O)(=O)c3ccc(cc3)-c3ccccc3C#N)CC2)nn1 | PDB
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TBA
| |
Citation and Details
BindingDB Entry DOI: 10.7270/Q2WH2V4R |
More data for this
Ligand-Target Pair | |
Casein kinase II subunit alpha
(Homo sapiens (Human)) | BDBM616452
(US20230278983, Code AB1135)Show SMILES CC(C)Cc1ccc(cc1)S(=O)(=O)NCCN1CCC(Cn2cc(nn2)-c2c([nH]c3ccc(F)cc23)C(C)=O)CC1 | PDB
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TBA
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Citation and Details
BindingDB Entry DOI: 10.7270/Q2WH2V4R |
More data for this
Ligand-Target Pair | |
Casein kinase II subunit alpha
(Homo sapiens (Human)) | BDBM616463
(US20230278983, Code AB1287)Show SMILES COc1cccc(CO)c1-c1ccc(cc1)S(=O)(=O)NCCN1CCC(Cn2cc(nn2)-c2c([nH]c3ccc(F)cc23)C(C)=O)CC1 | PDB
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TBA
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Citation and Details
BindingDB Entry DOI: 10.7270/Q2WH2V4R |
More data for this
Ligand-Target Pair | |
Casein kinase II subunit alpha
(Homo sapiens (Human)) | BDBM616450
(US20230278983, Code AB1130)Show SMILES CC(C)COC(=O)c1[nH]c2ccc(F)cc2c1-c1cn(CC2CCN(CCNS(=O)(=O)c3ccc(cc3)-c3c(C)noc3C)CC2)nn1 | PDB
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TBA
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Citation and Details
BindingDB Entry DOI: 10.7270/Q2WH2V4R |
More data for this
Ligand-Target Pair | |
Casein kinase II subunit alpha
(Homo sapiens (Human)) | BDBM616437
(US20230278983, Code AB935 | isobutyl 5-fluoro-3-(1...)Show SMILES CC(C)COC(=O)c1[nH]c2ccc(F)cc2c1-c1cn(CC2CCN(CCNS(=O)(=O)Cc3ccc(cc3)C(F)(F)F)CC2)nn1 | PDB
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TBA
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Citation and Details
BindingDB Entry DOI: 10.7270/Q2WH2V4R |
More data for this
Ligand-Target Pair | |
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