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Compile Data Set for Download or QSAR

Found 69 hits with Last Name = 'malmström' and Initial = 'j'   
Target/Host
(Institution)
LigandTarget/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
pHTemp
°C
Mitogen-activated protein kinase 10


(Homo sapiens (Human))
BDBM50172920
PNG
(3-(6-(2-chlorophenylamino)-1H-indazol-3-yl)-N-(pip...)
Show SMILES Clc1ccccc1Nc1ccc2c(n[nH]c2c1)-c1cccc(c1)C(=O)NC1CCNCC1
Show InChI InChI=1S/C25H24ClN5O/c26-21-6-1-2-7-22(21)28-19-8-9-20-23(15-19)30-31-24(20)16-4-3-5-17(14-16)25(32)29-18-10-12-27-13-11-18/h1-9,14-15,18,27-28H,10-13H2,(H,29,32)(H,30,31)
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n/an/a 1.40n/an/an/an/an/an/a



AstraZeneca R&D Södertälje

Curated by ChEMBL


Assay Description
Inhibitory concentration against c-Jun N-terminal kinase 3


Bioorg Med Chem Lett 15: 5095-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.06.083
BindingDB Entry DOI: 10.7270/Q2JW8DFC
More data for this
Ligand-Target Pair
Mitogen-activated protein kinase 10


(Homo sapiens (Human))
BDBM50211306
PNG
(4-(6-(2-chlorophenylamino)-1H-indazol-3-yl)-N-(2-(...)
Show SMILES CN(C)CCNC(=O)c1ccc(cc1)-c1n[nH]c2cc(Nc3ccccc3Cl)ccc12
Show InChI InChI=1S/C24H24ClN5O/c1-30(2)14-13-26-24(31)17-9-7-16(8-10-17)23-19-12-11-18(15-22(19)28-29-23)27-21-6-4-3-5-20(21)25/h3-12,15,27H,13-14H2,1-2H3,(H,26,31)(H,28,29)
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n/an/a 1.90n/an/an/an/an/an/a



AstraZeneca R&D Södertälje

Curated by ChEMBL


Assay Description
Inhibitory concentration against c-Jun N-terminal kinase 3


Bioorg Med Chem Lett 15: 5095-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.06.083
BindingDB Entry DOI: 10.7270/Q2JW8DFC
More data for this
Ligand-Target Pair
Mitogen-activated protein kinase 14


(Homo sapiens (Human))
BDBM50172919
PNG
(3-[6-(2-Chloro-phenylamino)-1H-indazol-3-yl]-benza...)
Show SMILES NC(=O)c1cccc(c1)-c1n[nH]c2cc(Nc3ccccc3Cl)ccc12
Show InChI InChI=1S/C20H15ClN4O/c21-16-6-1-2-7-17(16)23-14-8-9-15-18(11-14)24-25-19(15)12-4-3-5-13(10-12)20(22)26/h1-11,23H,(H2,22,26)(H,24,25)
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n/an/a 3.20n/an/an/an/an/an/a



AstraZeneca R&D Södertälje

Curated by ChEMBL


Assay Description
Inhibitory concentration against Mitogen-activated protein kinase p38 alpha


Bioorg Med Chem Lett 15: 5095-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.06.083
BindingDB Entry DOI: 10.7270/Q2JW8DFC
More data for this
Ligand-Target Pair
Mitogen-activated protein kinase 10


(Homo sapiens (Human))
BDBM50172919
PNG
(3-[6-(2-Chloro-phenylamino)-1H-indazol-3-yl]-benza...)
Show SMILES NC(=O)c1cccc(c1)-c1n[nH]c2cc(Nc3ccccc3Cl)ccc12
Show InChI InChI=1S/C20H15ClN4O/c21-16-6-1-2-7-17(16)23-14-8-9-15-18(11-14)24-25-19(15)12-4-3-5-13(10-12)20(22)26/h1-11,23H,(H2,22,26)(H,24,25)
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n/an/a 3.30n/an/an/an/an/an/a



AstraZeneca R&D Södertälje

Curated by ChEMBL


Assay Description
Inhibitory concentration against c-Jun N-terminal kinase 3


Bioorg Med Chem Lett 15: 5095-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.06.083
BindingDB Entry DOI: 10.7270/Q2JW8DFC
More data for this
Ligand-Target Pair
Mitogen-activated protein kinase 10


(Homo sapiens (Human))
BDBM50172921
PNG
(3-[6-(2-Chloro-phenylamino)-1H-indazol-3-yl]-N-(3-...)
Show SMILES Clc1ccccc1Nc1ccc2c(n[nH]c2c1)-c1cccc(c1)C(=O)NCCCN1CCOCC1
Show InChI InChI=1S/C27H28ClN5O2/c28-23-7-1-2-8-24(23)30-21-9-10-22-25(18-21)31-32-26(22)19-5-3-6-20(17-19)27(34)29-11-4-12-33-13-15-35-16-14-33/h1-3,5-10,17-18,30H,4,11-16H2,(H,29,34)(H,31,32)
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n/an/a 3.40n/an/an/an/an/an/a



AstraZeneca R&D Södertälje

Curated by ChEMBL


Assay Description
Inhibitory concentration against c-Jun N-terminal kinase 3


Bioorg Med Chem Lett 15: 5095-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.06.083
BindingDB Entry DOI: 10.7270/Q2JW8DFC
More data for this
Ligand-Target Pair
Mitogen-activated protein kinase 14


(Homo sapiens (Human))
BDBM50172921
PNG
(3-[6-(2-Chloro-phenylamino)-1H-indazol-3-yl]-N-(3-...)
Show SMILES Clc1ccccc1Nc1ccc2c(n[nH]c2c1)-c1cccc(c1)C(=O)NCCCN1CCOCC1
Show InChI InChI=1S/C27H28ClN5O2/c28-23-7-1-2-8-24(23)30-21-9-10-22-25(18-21)31-32-26(22)19-5-3-6-20(17-19)27(34)29-11-4-12-33-13-15-35-16-14-33/h1-3,5-10,17-18,30H,4,11-16H2,(H,29,34)(H,31,32)
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n/an/a 3.70n/an/an/an/an/an/a



AstraZeneca R&D Södertälje

Curated by ChEMBL


Assay Description
Inhibitory concentration against Mitogen-activated protein kinase p38 alpha


Bioorg Med Chem Lett 15: 5095-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.06.083
BindingDB Entry DOI: 10.7270/Q2JW8DFC
More data for this
Ligand-Target Pair
Mitogen-activated protein kinase 14


(Homo sapiens (Human))
BDBM50172920
PNG
(3-(6-(2-chlorophenylamino)-1H-indazol-3-yl)-N-(pip...)
Show SMILES Clc1ccccc1Nc1ccc2c(n[nH]c2c1)-c1cccc(c1)C(=O)NC1CCNCC1
Show InChI InChI=1S/C25H24ClN5O/c26-21-6-1-2-7-22(21)28-19-8-9-20-23(15-19)30-31-24(20)16-4-3-5-17(14-16)25(32)29-18-10-12-27-13-11-18/h1-9,14-15,18,27-28H,10-13H2,(H,29,32)(H,30,31)
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n/an/a 4.40n/an/an/an/an/an/a



AstraZeneca R&D Södertälje

Curated by ChEMBL


Assay Description
Inhibitory concentration against Mitogen-activated protein kinase p38 alpha


Bioorg Med Chem Lett 15: 5095-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.06.083
BindingDB Entry DOI: 10.7270/Q2JW8DFC
More data for this
Ligand-Target Pair
Mitogen-activated protein kinase 10


(Homo sapiens (Human))
BDBM50172927
PNG
(3-[6-(2-Chloro-phenylamino)-1H-indazol-3-yl]-benzo...)
Show SMILES OC(=O)c1cccc(c1)-c1n[nH]c2cc(Nc3ccccc3Cl)ccc12
Show InChI InChI=1S/C20H14ClN3O2/c21-16-6-1-2-7-17(16)22-14-8-9-15-18(11-14)23-24-19(15)12-4-3-5-13(10-12)20(25)26/h1-11,22H,(H,23,24)(H,25,26)
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n/an/a 5.30n/an/an/an/an/an/a



AstraZeneca R&D Södertälje

Curated by ChEMBL


Assay Description
Inhibitory concentration against c-Jun N-terminal kinase 3


Bioorg Med Chem Lett 15: 5095-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.06.083
BindingDB Entry DOI: 10.7270/Q2JW8DFC
More data for this
Ligand-Target Pair
Mitogen-activated protein kinase 14


(Homo sapiens (Human))
BDBM50211306
PNG
(4-(6-(2-chlorophenylamino)-1H-indazol-3-yl)-N-(2-(...)
Show SMILES CN(C)CCNC(=O)c1ccc(cc1)-c1n[nH]c2cc(Nc3ccccc3Cl)ccc12
Show InChI InChI=1S/C24H24ClN5O/c1-30(2)14-13-26-24(31)17-9-7-16(8-10-17)23-19-12-11-18(15-22(19)28-29-23)27-21-6-4-3-5-20(21)25/h3-12,15,27H,13-14H2,1-2H3,(H,26,31)(H,28,29)
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n/an/a 8.70n/an/an/an/an/an/a



AstraZeneca R&D Södertälje

Curated by ChEMBL


Assay Description
Inhibitory concentration against Mitogen-activated protein kinase p38 alpha


Bioorg Med Chem Lett 15: 5095-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.06.083
BindingDB Entry DOI: 10.7270/Q2JW8DFC
More data for this
Ligand-Target Pair
Mitogen-activated protein kinase 14


(Homo sapiens (Human))
BDBM50172922
PNG
(4-[6-(2-Chloro-phenylamino)-1H-indazol-3-yl]-benzo...)
Show SMILES OC(=O)c1ccc(cc1)-c1n[nH]c2cc(Nc3ccccc3Cl)ccc12
Show InChI InChI=1S/C20H14ClN3O2/c21-16-3-1-2-4-17(16)22-14-9-10-15-18(11-14)23-24-19(15)12-5-7-13(8-6-12)20(25)26/h1-11,22H,(H,23,24)(H,25,26)
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n/an/a 13n/an/an/an/an/an/a



AstraZeneca R&D Södertälje

Curated by ChEMBL


Assay Description
Inhibitory concentration against Mitogen-activated protein kinase p38 alpha


Bioorg Med Chem Lett 15: 5095-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.06.083
BindingDB Entry DOI: 10.7270/Q2JW8DFC
More data for this
Ligand-Target Pair
Mitogen-activated protein kinase 14


(Homo sapiens (Human))
BDBM50172923
PNG
(3-[6-(2-Chloro-phenylamino)-1H-indazol-3-yl]-N-(2-...)
Show SMILES CN(C)CCNC(=O)c1cccc(c1)-c1n[nH]c2cc(Nc3ccccc3Cl)ccc12
Show InChI InChI=1S/C24H24ClN5O/c1-30(2)13-12-26-24(31)17-7-5-6-16(14-17)23-19-11-10-18(15-22(19)28-29-23)27-21-9-4-3-8-20(21)25/h3-11,14-15,27H,12-13H2,1-2H3,(H,26,31)(H,28,29)
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n/an/a 16n/an/an/an/an/an/a



AstraZeneca R&D Södertälje

Curated by ChEMBL


Assay Description
Inhibitory concentration against Mitogen-activated protein kinase p38 alpha


Bioorg Med Chem Lett 15: 5095-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.06.083
BindingDB Entry DOI: 10.7270/Q2JW8DFC
More data for this
Ligand-Target Pair
Mitogen-activated protein kinase 14


(Homo sapiens (Human))
BDBM50172918
PNG
((2-Chloro-phenyl)-(3-phenyl-1H-indazol-6-yl)-amine...)
Show SMILES Clc1ccccc1Nc1ccc2c(n[nH]c2c1)-c1ccccc1
Show InChI InChI=1S/C19H14ClN3/c20-16-8-4-5-9-17(16)21-14-10-11-15-18(12-14)22-23-19(15)13-6-2-1-3-7-13/h1-12,21H,(H,22,23)
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n/an/a 18n/an/an/an/an/an/a



AstraZeneca R&D Södertälje

Curated by ChEMBL


Assay Description
Inhibitory concentration against Mitogen-activated protein kinase p38 alpha


Bioorg Med Chem Lett 15: 5095-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.06.083
BindingDB Entry DOI: 10.7270/Q2JW8DFC
More data for this
Ligand-Target Pair
Mitogen-activated protein kinase 10


(Homo sapiens (Human))
BDBM50172923
PNG
(3-[6-(2-Chloro-phenylamino)-1H-indazol-3-yl]-N-(2-...)
Show SMILES CN(C)CCNC(=O)c1cccc(c1)-c1n[nH]c2cc(Nc3ccccc3Cl)ccc12
Show InChI InChI=1S/C24H24ClN5O/c1-30(2)13-12-26-24(31)17-7-5-6-16(14-17)23-19-11-10-18(15-22(19)28-29-23)27-21-9-4-3-8-20(21)25/h3-11,14-15,27H,12-13H2,1-2H3,(H,26,31)(H,28,29)
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n/an/a 21n/an/an/an/an/an/a



AstraZeneca R&D Södertälje

Curated by ChEMBL


Assay Description
Inhibitory concentration against c-Jun N-terminal kinase 3


Bioorg Med Chem Lett 15: 5095-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.06.083
BindingDB Entry DOI: 10.7270/Q2JW8DFC
More data for this
Ligand-Target Pair
Metabotropic glutamate receptor 5


(Homo sapiens (Human))
BDBM50084137
PNG
(2-Methyl-6-(phenylethynyl)pyridine | 2-Methyl-6-ph...)
Show SMILES Cc1cccc(n1)C#Cc1ccccc1
Show InChI InChI=1S/C14H11N/c1-12-6-5-9-14(15-12)11-10-13-7-3-2-4-8-13/h2-9H,1H3
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n/an/a 22n/an/an/an/an/an/a



NPS Pharmaceuticals Inc

Curated by ChEMBL


Assay Description
Inhibition of glutamate-induced calcium influx in human mGluR5d by FLIPR


Bioorg Med Chem Lett 16: 2467-9 (2006)


Article DOI: 10.1016/j.bmcl.2006.01.100
BindingDB Entry DOI: 10.7270/Q22Z1544
More data for this
Ligand-Target Pair
Mitogen-activated protein kinase 14


(Homo sapiens (Human))
BDBM50172927
PNG
(3-[6-(2-Chloro-phenylamino)-1H-indazol-3-yl]-benzo...)
Show SMILES OC(=O)c1cccc(c1)-c1n[nH]c2cc(Nc3ccccc3Cl)ccc12
Show InChI InChI=1S/C20H14ClN3O2/c21-16-6-1-2-7-17(16)22-14-8-9-15-18(11-14)23-24-19(15)12-4-3-5-13(10-12)20(25)26/h1-11,22H,(H,23,24)(H,25,26)
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n/an/a 24n/an/an/an/an/an/a



AstraZeneca R&D Södertälje

Curated by ChEMBL


Assay Description
Inhibitory concentration against Mitogen-activated protein kinase p38 alpha


Bioorg Med Chem Lett 15: 5095-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.06.083
BindingDB Entry DOI: 10.7270/Q2JW8DFC
More data for this
Ligand-Target Pair
Mitogen-activated protein kinase 14


(Homo sapiens (Human))
BDBM50172925
PNG
(CHEMBL383177 | N,3-diphenyl-1H-indazol-6-amine | P...)
Show SMILES N(c1ccccc1)c1ccc2c(n[nH]c2c1)-c1ccccc1
Show InChI InChI=1S/C19H15N3/c1-3-7-14(8-4-1)19-17-12-11-16(13-18(17)21-22-19)20-15-9-5-2-6-10-15/h1-13,20H,(H,21,22)
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n/an/a 30n/an/an/an/an/an/a



AstraZeneca R&D Södertälje

Curated by ChEMBL


Assay Description
Inhibitory concentration against Mitogen-activated protein kinase p38 alpha


Bioorg Med Chem Lett 15: 5095-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.06.083
BindingDB Entry DOI: 10.7270/Q2JW8DFC
More data for this
Ligand-Target Pair
Mitogen-activated protein kinase 10


(Homo sapiens (Human))
BDBM50172918
PNG
((2-Chloro-phenyl)-(3-phenyl-1H-indazol-6-yl)-amine...)
Show SMILES Clc1ccccc1Nc1ccc2c(n[nH]c2c1)-c1ccccc1
Show InChI InChI=1S/C19H14ClN3/c20-16-8-4-5-9-17(16)21-14-10-11-15-18(12-14)22-23-19(15)13-6-2-1-3-7-13/h1-12,21H,(H,22,23)
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n/an/a 30n/an/an/an/an/an/a



AstraZeneca R&D Södertälje

Curated by ChEMBL


Assay Description
Inhibitory concentration against c-Jun N-terminal kinase 3


Bioorg Med Chem Lett 15: 5095-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.06.083
BindingDB Entry DOI: 10.7270/Q2JW8DFC
More data for this
Ligand-Target Pair
Mitogen-activated protein kinase 10


(Homo sapiens (Human))
BDBM50172922
PNG
(4-[6-(2-Chloro-phenylamino)-1H-indazol-3-yl]-benzo...)
Show SMILES OC(=O)c1ccc(cc1)-c1n[nH]c2cc(Nc3ccccc3Cl)ccc12
Show InChI InChI=1S/C20H14ClN3O2/c21-16-3-1-2-4-17(16)22-14-9-10-15-18(11-14)23-24-19(15)12-5-7-13(8-6-12)20(25)26/h1-11,22H,(H,23,24)(H,25,26)
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n/an/a 32n/an/an/an/an/an/a



AstraZeneca R&D Södertälje

Curated by ChEMBL


Assay Description
Inhibitory concentration against c-Jun N-terminal kinase 3


Bioorg Med Chem Lett 15: 5095-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.06.083
BindingDB Entry DOI: 10.7270/Q2JW8DFC
More data for this
Ligand-Target Pair
c-Jun N-terminal kinase, JNK


(Homo sapiens (Human))
BDBM50211306
PNG
(4-(6-(2-chlorophenylamino)-1H-indazol-3-yl)-N-(2-(...)
Show SMILES CN(C)CCNC(=O)c1ccc(cc1)-c1n[nH]c2cc(Nc3ccccc3Cl)ccc12
Show InChI InChI=1S/C24H24ClN5O/c1-30(2)14-13-26-24(31)17-9-7-16(8-10-17)23-19-12-11-18(15-22(19)28-29-23)27-21-6-4-3-5-20(21)25/h3-12,15,27H,13-14H2,1-2H3,(H,26,31)(H,28,29)
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n/an/a 45n/an/an/an/an/an/a



AstraZeneca R&D Södertälje

Curated by ChEMBL


Assay Description
Inhibitory concentration against c-Jun N-terminal kinase 1


Bioorg Med Chem Lett 15: 5095-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.06.083
BindingDB Entry DOI: 10.7270/Q2JW8DFC
More data for this
Ligand-Target Pair
Mitogen-activated protein kinase 14


(Homo sapiens (Human))
BDBM50211303
PNG
((2-Methoxy-phenyl)-(3-phenyl-1H-indazol-6-yl)-amin...)
Show SMILES COc1ccccc1Nc1ccc2c(n[nH]c2c1)-c1ccccc1
Show InChI InChI=1S/C20H17N3O/c1-24-19-10-6-5-9-17(19)21-15-11-12-16-18(13-15)22-23-20(16)14-7-3-2-4-8-14/h2-13,21H,1H3,(H,22,23)
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n/an/a 46n/an/an/an/an/an/a



AstraZeneca R&D Södertälje

Curated by ChEMBL


Assay Description
Inhibitory concentration against Mitogen-activated protein kinase p38 alpha


Bioorg Med Chem Lett 15: 5095-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.06.083
BindingDB Entry DOI: 10.7270/Q2JW8DFC
More data for this
Ligand-Target Pair
Mitogen-activated protein kinase 10


(Homo sapiens (Human))
BDBM50172925
PNG
(CHEMBL383177 | N,3-diphenyl-1H-indazol-6-amine | P...)
Show SMILES N(c1ccccc1)c1ccc2c(n[nH]c2c1)-c1ccccc1
Show InChI InChI=1S/C19H15N3/c1-3-7-14(8-4-1)19-17-12-11-16(13-18(17)21-22-19)20-15-9-5-2-6-10-15/h1-13,20H,(H,21,22)
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n/an/a 48n/an/an/an/an/an/a



AstraZeneca R&D Södertälje

Curated by ChEMBL


Assay Description
Inhibitory concentration against c-Jun N-terminal kinase 3


Bioorg Med Chem Lett 15: 5095-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.06.083
BindingDB Entry DOI: 10.7270/Q2JW8DFC
More data for this
Ligand-Target Pair
c-Jun N-terminal kinase, JNK


(Homo sapiens (Human))
BDBM50172927
PNG
(3-[6-(2-Chloro-phenylamino)-1H-indazol-3-yl]-benzo...)
Show SMILES OC(=O)c1cccc(c1)-c1n[nH]c2cc(Nc3ccccc3Cl)ccc12
Show InChI InChI=1S/C20H14ClN3O2/c21-16-6-1-2-7-17(16)22-14-8-9-15-18(11-14)23-24-19(15)12-4-3-5-13(10-12)20(25)26/h1-11,22H,(H,23,24)(H,25,26)
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n/an/a 61n/an/an/an/an/an/a



AstraZeneca R&D Södertälje

Curated by ChEMBL


Assay Description
Inhibitory concentration against c-Jun N-terminal kinase 1


Bioorg Med Chem Lett 15: 5095-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.06.083
BindingDB Entry DOI: 10.7270/Q2JW8DFC
More data for this
Ligand-Target Pair
c-Jun N-terminal kinase, JNK


(Homo sapiens (Human))
BDBM50172920
PNG
(3-(6-(2-chlorophenylamino)-1H-indazol-3-yl)-N-(pip...)
Show SMILES Clc1ccccc1Nc1ccc2c(n[nH]c2c1)-c1cccc(c1)C(=O)NC1CCNCC1
Show InChI InChI=1S/C25H24ClN5O/c26-21-6-1-2-7-22(21)28-19-8-9-20-23(15-19)30-31-24(20)16-4-3-5-17(14-16)25(32)29-18-10-12-27-13-11-18/h1-9,14-15,18,27-28H,10-13H2,(H,29,32)(H,30,31)
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n/an/a 71n/an/an/an/an/an/a



AstraZeneca R&D Södertälje

Curated by ChEMBL


Assay Description
Inhibitory concentration against c-Jun N-terminal kinase 1


Bioorg Med Chem Lett 15: 5095-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.06.083
BindingDB Entry DOI: 10.7270/Q2JW8DFC
More data for this
Ligand-Target Pair
Metabotropic glutamate receptor 5


(Homo sapiens (Human))
BDBM50182823
PNG
(4-(3,4-dichlorophenylthio)-2-(5-fluoropyridin-2-yl...)
Show SMILES Fc1ccc(nc1)-c1nccc(Sc2ccc(Cl)c(Cl)c2)n1
Show InChI InChI=1S/C15H8Cl2FN3S/c16-11-3-2-10(7-12(11)17)22-14-5-6-19-15(21-14)13-4-1-9(18)8-20-13/h1-8H
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n/an/a 80n/an/an/an/an/an/a



NPS Pharmaceuticals Inc

Curated by ChEMBL


Assay Description
Inhibition of glutamate-induced calcium influx in human mGluR5d by FLIPR


Bioorg Med Chem Lett 16: 2467-9 (2006)


Article DOI: 10.1016/j.bmcl.2006.01.100
BindingDB Entry DOI: 10.7270/Q22Z1544
More data for this
Ligand-Target Pair
c-Jun N-terminal kinase, JNK


(Homo sapiens (Human))
BDBM50172919
PNG
(3-[6-(2-Chloro-phenylamino)-1H-indazol-3-yl]-benza...)
Show SMILES NC(=O)c1cccc(c1)-c1n[nH]c2cc(Nc3ccccc3Cl)ccc12
Show InChI InChI=1S/C20H15ClN4O/c21-16-6-1-2-7-17(16)23-14-8-9-15-18(11-14)24-25-19(15)12-4-3-5-13(10-12)20(22)26/h1-11,23H,(H2,22,26)(H,24,25)
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n/an/a 81n/an/an/an/an/an/a



AstraZeneca R&D Södertälje

Curated by ChEMBL


Assay Description
Inhibitory concentration against c-Jun N-terminal kinase 1


Bioorg Med Chem Lett 15: 5095-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.06.083
BindingDB Entry DOI: 10.7270/Q2JW8DFC
More data for this
Ligand-Target Pair
Metabotropic glutamate receptor 5


(Homo sapiens (Human))
BDBM50182811
PNG
(4-(3,4-dichlorophenylthio)-2-(pyridin-2-yl)pyrimid...)
Show SMILES Clc1ccc(Sc2ccnc(n2)-c2ccccn2)cc1Cl
Show InChI InChI=1S/C15H9Cl2N3S/c16-11-5-4-10(9-12(11)17)21-14-6-8-19-15(20-14)13-3-1-2-7-18-13/h1-9H
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n/an/a 90n/an/an/an/an/an/a



NPS Pharmaceuticals Inc

Curated by ChEMBL


Assay Description
Inhibition of glutamate-induced calcium influx in human mGluR5d by FLIPR


Bioorg Med Chem Lett 16: 2467-9 (2006)


Article DOI: 10.1016/j.bmcl.2006.01.100
BindingDB Entry DOI: 10.7270/Q22Z1544
More data for this
Ligand-Target Pair
Mitogen-activated protein kinase 10


(Homo sapiens (Human))
BDBM50211303
PNG
((2-Methoxy-phenyl)-(3-phenyl-1H-indazol-6-yl)-amin...)
Show SMILES COc1ccccc1Nc1ccc2c(n[nH]c2c1)-c1ccccc1
Show InChI InChI=1S/C20H17N3O/c1-24-19-10-6-5-9-17(19)21-15-11-12-16-18(13-15)22-23-20(16)14-7-3-2-4-8-14/h2-13,21H,1H3,(H,22,23)
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n/an/a 202n/an/an/an/an/an/a



AstraZeneca R&D Södertälje

Curated by ChEMBL


Assay Description
Inhibitory concentration against c-Jun N-terminal kinase 3


Bioorg Med Chem Lett 15: 5095-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.06.083
BindingDB Entry DOI: 10.7270/Q2JW8DFC
More data for this
Ligand-Target Pair
Metabotropic glutamate receptor 5


(Homo sapiens (Human))
BDBM50182813
PNG
(2-(pyridin-2-yl)-4-(4-(trifluoromethyl)phenylthio)...)
Show SMILES FC(F)(F)c1ccc(Sc2ccnc(n2)-c2ccccn2)cc1
Show InChI InChI=1S/C16H10F3N3S/c17-16(18,19)11-4-6-12(7-5-11)23-14-8-10-21-15(22-14)13-3-1-2-9-20-13/h1-10H
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n/an/a 210n/an/an/an/an/an/a



NPS Pharmaceuticals Inc

Curated by ChEMBL


Assay Description
Inhibition of glutamate-induced calcium influx in human mGluR5d by FLIPR


Bioorg Med Chem Lett 16: 2467-9 (2006)


Article DOI: 10.1016/j.bmcl.2006.01.100
BindingDB Entry DOI: 10.7270/Q22Z1544
More data for this
Ligand-Target Pair
c-Jun N-terminal kinase, JNK


(Homo sapiens (Human))
BDBM50172921
PNG
(3-[6-(2-Chloro-phenylamino)-1H-indazol-3-yl]-N-(3-...)
Show SMILES Clc1ccccc1Nc1ccc2c(n[nH]c2c1)-c1cccc(c1)C(=O)NCCCN1CCOCC1
Show InChI InChI=1S/C27H28ClN5O2/c28-23-7-1-2-8-24(23)30-21-9-10-22-25(18-21)31-32-26(22)19-5-3-6-20(17-19)27(34)29-11-4-12-33-13-15-35-16-14-33/h1-3,5-10,17-18,30H,4,11-16H2,(H,29,34)(H,31,32)
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n/an/a 228n/an/an/an/an/an/a



AstraZeneca R&D Södertälje

Curated by ChEMBL


Assay Description
Inhibitory concentration against c-Jun N-terminal kinase 1


Bioorg Med Chem Lett 15: 5095-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.06.083
BindingDB Entry DOI: 10.7270/Q2JW8DFC
More data for this
Ligand-Target Pair
c-Jun N-terminal kinase, JNK


(Homo sapiens (Human))
BDBM50172922
PNG
(4-[6-(2-Chloro-phenylamino)-1H-indazol-3-yl]-benzo...)
Show SMILES OC(=O)c1ccc(cc1)-c1n[nH]c2cc(Nc3ccccc3Cl)ccc12
Show InChI InChI=1S/C20H14ClN3O2/c21-16-3-1-2-4-17(16)22-14-9-10-15-18(11-14)23-24-19(15)12-5-7-13(8-6-12)20(25)26/h1-11,22H,(H,23,24)(H,25,26)
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n/an/a 246n/an/an/an/an/an/a



AstraZeneca R&D Södertälje

Curated by ChEMBL


Assay Description
Inhibitory concentration against c-Jun N-terminal kinase 1


Bioorg Med Chem Lett 15: 5095-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.06.083
BindingDB Entry DOI: 10.7270/Q2JW8DFC
More data for this
Ligand-Target Pair
Metabotropic glutamate receptor 5


(Homo sapiens (Human))
BDBM50182822
PNG
(4-(4-chlorophenylthio)-2-(pyridin-2-yl)pyrimidine ...)
Show SMILES Clc1ccc(Sc2ccnc(n2)-c2ccccn2)cc1
Show InChI InChI=1S/C15H10ClN3S/c16-11-4-6-12(7-5-11)20-14-8-10-18-15(19-14)13-3-1-2-9-17-13/h1-10H
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n/an/a 320n/an/an/an/an/an/a



NPS Pharmaceuticals Inc

Curated by ChEMBL


Assay Description
Inhibition of glutamate-induced calcium influx in human mGluR5d by FLIPR


Bioorg Med Chem Lett 16: 2467-9 (2006)


Article DOI: 10.1016/j.bmcl.2006.01.100
BindingDB Entry DOI: 10.7270/Q22Z1544
More data for this
Ligand-Target Pair
Cyclin-Dependent Kinase 5 (CDK5)


(Homo sapiens (Human))
BDBM50390639
PNG
(CHEMBL2069712)
Show SMILES NS(=O)(=O)c1cc(cs1)-c1nc2ccc(F)cc2s1
Show InChI InChI=1S/C11H7FN2O2S3/c12-7-1-2-8-9(4-7)18-11(14-8)6-3-10(17-5-6)19(13,15)16/h1-5H,(H2,13,15,16)
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n/an/a 331n/an/an/an/an/an/a



AstraZeneca

Curated by ChEMBL


Assay Description
Inhibition of human recombinant Cdk5/p25 incubated for 15 mins by scintillation proximity assay


Bioorg Med Chem Lett 22: 5919-23 (2012)


Article DOI: 10.1016/j.bmcl.2012.07.068
BindingDB Entry DOI: 10.7270/Q2G73FTN
More data for this
Ligand-Target Pair
Cyclin-Dependent Kinase 5 (CDK5)


(Homo sapiens (Human))
BDBM50390640
PNG
(CHEMBL2069713)
Show SMILES NS(=O)(=O)c1cc(cs1)-c1nc2ccc(Cl)cc2s1
Show InChI InChI=1S/C11H7ClN2O2S3/c12-7-1-2-8-9(4-7)18-11(14-8)6-3-10(17-5-6)19(13,15)16/h1-5H,(H2,13,15,16)
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n/an/a 355n/an/an/an/an/an/a



AstraZeneca

Curated by ChEMBL


Assay Description
Inhibition of human recombinant Cdk5/p25 incubated for 15 mins by scintillation proximity assay


Bioorg Med Chem Lett 22: 5919-23 (2012)


Article DOI: 10.1016/j.bmcl.2012.07.068
BindingDB Entry DOI: 10.7270/Q2G73FTN
More data for this
Ligand-Target Pair
Metabotropic glutamate receptor 5


(Homo sapiens (Human))
BDBM50182819
PNG
(4-(3,4-dichlorophenylthio)-2-(6-methylpyridin-2-yl...)
Show SMILES Cc1cccc(n1)-c1nccc(Sc2ccc(Cl)c(Cl)c2)n1
Show InChI InChI=1S/C16H11Cl2N3S/c1-10-3-2-4-14(20-10)16-19-8-7-15(21-16)22-11-5-6-12(17)13(18)9-11/h2-9H,1H3
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n/an/a 390n/an/an/an/an/an/a



NPS Pharmaceuticals Inc

Curated by ChEMBL


Assay Description
Inhibition of glutamate-induced calcium influx in human mGluR5d by FLIPR


Bioorg Med Chem Lett 16: 2467-9 (2006)


Article DOI: 10.1016/j.bmcl.2006.01.100
BindingDB Entry DOI: 10.7270/Q22Z1544
More data for this
Ligand-Target Pair
Metabotropic glutamate receptor 5


(Homo sapiens (Human))
BDBM50182816
PNG
(2-(pyridin-2-yl)-4-(3-(trifluoromethyl)phenylthio)...)
Show SMILES FC(F)(F)c1cccc(Sc2ccnc(n2)-c2ccccn2)c1
Show InChI InChI=1S/C16H10F3N3S/c17-16(18,19)11-4-3-5-12(10-11)23-14-7-9-21-15(22-14)13-6-1-2-8-20-13/h1-10H
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n/an/a 550n/an/an/an/an/an/a



NPS Pharmaceuticals Inc

Curated by ChEMBL


Assay Description
Inhibition of glutamate-induced calcium influx in human mGluR5d by FLIPR


Bioorg Med Chem Lett 16: 2467-9 (2006)


Article DOI: 10.1016/j.bmcl.2006.01.100
BindingDB Entry DOI: 10.7270/Q22Z1544
More data for this
Ligand-Target Pair
Cyclin-Dependent Kinase 5 (CDK5)


(Homo sapiens (Human))
BDBM50390638
PNG
(CHEMBL2069711)
Show SMILES NS(=O)(=O)c1cc(cs1)-c1nc2ccccc2s1
Show InChI InChI=1S/C11H8N2O2S3/c12-18(14,15)10-5-7(6-16-10)11-13-8-3-1-2-4-9(8)17-11/h1-6H,(H2,12,14,15)
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n/an/a 551n/an/an/an/an/an/a



AstraZeneca

Curated by ChEMBL


Assay Description
Inhibition of human recombinant Cdk5/p25 incubated for 15 mins by scintillation proximity assay


Bioorg Med Chem Lett 22: 5919-23 (2012)


Article DOI: 10.1016/j.bmcl.2012.07.068
BindingDB Entry DOI: 10.7270/Q2G73FTN
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Metabotropic glutamate receptor 5


(Homo sapiens (Human))
BDBM50182809
PNG
(4-(3-chlorophenylthio)-2-(pyridin-2-yl)pyrimidine ...)
Show SMILES Clc1cccc(Sc2ccnc(n2)-c2ccccn2)c1
Show InChI InChI=1S/C15H10ClN3S/c16-11-4-3-5-12(10-11)20-14-7-9-18-15(19-14)13-6-1-2-8-17-13/h1-10H
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n/an/a 620n/an/an/an/an/an/a



NPS Pharmaceuticals Inc

Curated by ChEMBL


Assay Description
Inhibition of glutamate-induced calcium influx in human mGluR5d by FLIPR


Bioorg Med Chem Lett 16: 2467-9 (2006)


Article DOI: 10.1016/j.bmcl.2006.01.100
BindingDB Entry DOI: 10.7270/Q22Z1544
More data for this
Ligand-Target Pair
Cyclin-Dependent Kinase 5 (CDK5)


(Homo sapiens (Human))
BDBM50390653
PNG
(CHEMBL2069727)
Show SMILES NS(=O)(=O)c1cc(cs1)-c1nc2ccc(F)c(Cl)c2s1
Show InChI InChI=1S/C11H6ClFN2O2S3/c12-9-6(13)1-2-7-10(9)19-11(15-7)5-3-8(18-4-5)20(14,16)17/h1-4H,(H2,14,16,17)
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n/an/a 672n/an/an/an/an/an/a



AstraZeneca

Curated by ChEMBL


Assay Description
Inhibition of human recombinant Cdk5/p25 incubated for 15 mins by scintillation proximity assay


Bioorg Med Chem Lett 22: 5919-23 (2012)


Article DOI: 10.1016/j.bmcl.2012.07.068
BindingDB Entry DOI: 10.7270/Q2G73FTN
More data for this
Ligand-Target Pair
c-Jun N-terminal kinase, JNK


(Homo sapiens (Human))
BDBM50172923
PNG
(3-[6-(2-Chloro-phenylamino)-1H-indazol-3-yl]-N-(2-...)
Show SMILES CN(C)CCNC(=O)c1cccc(c1)-c1n[nH]c2cc(Nc3ccccc3Cl)ccc12
Show InChI InChI=1S/C24H24ClN5O/c1-30(2)13-12-26-24(31)17-7-5-6-16(14-17)23-19-11-10-18(15-22(19)28-29-23)27-21-9-4-3-8-20(21)25/h3-11,14-15,27H,12-13H2,1-2H3,(H,26,31)(H,28,29)
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n/an/a 698n/an/an/an/an/an/a



AstraZeneca R&D Södertälje

Curated by ChEMBL


Assay Description
Inhibitory concentration against c-Jun N-terminal kinase 1


Bioorg Med Chem Lett 15: 5095-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.06.083
BindingDB Entry DOI: 10.7270/Q2JW8DFC
More data for this
Ligand-Target Pair
Metabotropic glutamate receptor 5


(Homo sapiens (Human))
BDBM50182814
PNG
(4-(4-chlorophenylthio)-6-methyl-2-(pyridin-2-yl)py...)
Show SMILES Cc1cc(Sc2ccc(Cl)cc2)nc(n1)-c1ccccn1
Show InChI InChI=1S/C16H12ClN3S/c1-11-10-15(21-13-7-5-12(17)6-8-13)20-16(19-11)14-4-2-3-9-18-14/h2-10H,1H3
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n/an/a 1.25E+3n/an/an/an/an/an/a



NPS Pharmaceuticals Inc

Curated by ChEMBL


Assay Description
Inhibition of glutamate-induced calcium influx in human mGluR5d by FLIPR


Bioorg Med Chem Lett 16: 2467-9 (2006)


Article DOI: 10.1016/j.bmcl.2006.01.100
BindingDB Entry DOI: 10.7270/Q22Z1544
More data for this
Ligand-Target Pair
Cyclin-Dependent Kinase 5 (CDK5)


(Homo sapiens (Human))
BDBM50390641
PNG
(CHEMBL2069714)
Show SMILES Cc1ccc2nc(sc2c1)-c1csc(c1)S(N)(=O)=O
Show InChI InChI=1S/C12H10N2O2S3/c1-7-2-3-9-10(4-7)18-12(14-9)8-5-11(17-6-8)19(13,15)16/h2-6H,1H3,(H2,13,15,16)
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n/an/a 1.26E+3n/an/an/an/an/an/a



AstraZeneca

Curated by ChEMBL


Assay Description
Inhibition of human recombinant Cdk5/p25 incubated for 15 mins by scintillation proximity assay


Bioorg Med Chem Lett 22: 5919-23 (2012)


Article DOI: 10.1016/j.bmcl.2012.07.068
BindingDB Entry DOI: 10.7270/Q2G73FTN
More data for this
Ligand-Target Pair
Cyclin-Dependent Kinase 5 (CDK5)


(Homo sapiens (Human))
BDBM50390642
PNG
(CHEMBL2069715)
Show SMILES NS(=O)(=O)c1cc(cs1)-c1nc2ccc(cc2s1)[N+]([O-])=O
Show InChI InChI=1S/C11H7N3O4S3/c12-21(17,18)10-3-6(5-19-10)11-13-8-2-1-7(14(15)16)4-9(8)20-11/h1-5H,(H2,12,17,18)
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n/an/a 1.27E+3n/an/an/an/an/an/a



AstraZeneca

Curated by ChEMBL


Assay Description
Inhibition of human recombinant Cdk5/p25 incubated for 15 mins by scintillation proximity assay


Bioorg Med Chem Lett 22: 5919-23 (2012)


Article DOI: 10.1016/j.bmcl.2012.07.068
BindingDB Entry DOI: 10.7270/Q2G73FTN
More data for this
Ligand-Target Pair
Metabotropic glutamate receptor 5


(Homo sapiens (Human))
BDBM50182821
PNG
(4-(3,4-difluorophenylthio)-2-(pyridin-2-yl)pyrimid...)
Show SMILES Fc1ccc(Sc2ccnc(n2)-c2ccccn2)cc1F
Show InChI InChI=1S/C15H9F2N3S/c16-11-5-4-10(9-12(11)17)21-14-6-8-19-15(20-14)13-3-1-2-7-18-13/h1-9H
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n/an/a 1.52E+3n/an/an/an/an/an/a



NPS Pharmaceuticals Inc

Curated by ChEMBL


Assay Description
Inhibition of glutamate-induced calcium influx in human mGluR5d by FLIPR


Bioorg Med Chem Lett 16: 2467-9 (2006)


Article DOI: 10.1016/j.bmcl.2006.01.100
BindingDB Entry DOI: 10.7270/Q22Z1544
More data for this
Ligand-Target Pair
c-Jun N-terminal kinase, JNK


(Homo sapiens (Human))
BDBM50211303
PNG
((2-Methoxy-phenyl)-(3-phenyl-1H-indazol-6-yl)-amin...)
Show SMILES COc1ccccc1Nc1ccc2c(n[nH]c2c1)-c1ccccc1
Show InChI InChI=1S/C20H17N3O/c1-24-19-10-6-5-9-17(19)21-15-11-12-16-18(13-15)22-23-20(16)14-7-3-2-4-8-14/h2-13,21H,1H3,(H,22,23)
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n/an/a 1.60E+3n/an/an/an/an/an/a



AstraZeneca R&D Södertälje

Curated by ChEMBL


Assay Description
Inhibitory concentration against c-Jun N-terminal kinase 1


Bioorg Med Chem Lett 15: 5095-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.06.083
BindingDB Entry DOI: 10.7270/Q2JW8DFC
More data for this
Ligand-Target Pair
Cyclin-Dependent Kinase 5 (CDK5)


(Homo sapiens (Human))
BDBM50390645
PNG
(CHEMBL2069719)
Show SMILES O=S(=O)(Nc1nccs1)c1cc(cs1)-c1nc2ccccc2s1
Show InChI InChI=1S/C14H9N3O2S4/c18-23(19,17-14-15-5-6-20-14)12-7-9(8-21-12)13-16-10-3-1-2-4-11(10)22-13/h1-8H,(H,15,17)
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n/an/a 1.76E+3n/an/an/an/an/an/a



AstraZeneca

Curated by ChEMBL


Assay Description
Inhibition of human recombinant Cdk5/p25 incubated for 15 mins by scintillation proximity assay


Bioorg Med Chem Lett 22: 5919-23 (2012)


Article DOI: 10.1016/j.bmcl.2012.07.068
BindingDB Entry DOI: 10.7270/Q2G73FTN
More data for this
Ligand-Target Pair
Metabotropic glutamate receptor 5


(Homo sapiens (Human))
BDBM50182815
PNG
(2-(pyridin-2-yl)-4-(m-tolylthio)pyrimidine | CHEMB...)
Show SMILES Cc1cccc(Sc2ccnc(n2)-c2ccccn2)c1
Show InChI InChI=1S/C16H13N3S/c1-12-5-4-6-13(11-12)20-15-8-10-18-16(19-15)14-7-2-3-9-17-14/h2-11H,1H3
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n/an/a 2.30E+3n/an/an/an/an/an/a



NPS Pharmaceuticals Inc

Curated by ChEMBL


Assay Description
Inhibition of glutamate-induced calcium influx in human mGluR5d by FLIPR


Bioorg Med Chem Lett 16: 2467-9 (2006)


Article DOI: 10.1016/j.bmcl.2006.01.100
BindingDB Entry DOI: 10.7270/Q22Z1544
More data for this
Ligand-Target Pair
Metabotropic glutamate receptor 5


(Homo sapiens (Human))
BDBM50182812
PNG
(2-(4-(3,4-dichlorophenylthio)pyridin-2-yl)pyridine...)
Show SMILES Clc1ccc(Sc2ccnc(c2)-c2ccccn2)cc1Cl
Show InChI InChI=1S/C16H10Cl2N2S/c17-13-5-4-11(9-14(13)18)21-12-6-8-20-16(10-12)15-3-1-2-7-19-15/h1-10H
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n/an/a 2.37E+3n/an/an/an/an/an/a



NPS Pharmaceuticals Inc

Curated by ChEMBL


Assay Description
Inhibition of glutamate-induced calcium influx in human mGluR5d by FLIPR


Bioorg Med Chem Lett 16: 2467-9 (2006)


Article DOI: 10.1016/j.bmcl.2006.01.100
BindingDB Entry DOI: 10.7270/Q22Z1544
More data for this
Ligand-Target Pair
Metabotropic glutamate receptor 5


(Homo sapiens (Human))
BDBM50182817
PNG
(4-(3-bromophenylthio)-2-(pyridin-2-yl)pyrimidine |...)
Show SMILES Brc1cccc(Sc2ccnc(n2)-c2ccccn2)c1
Show InChI InChI=1S/C15H10BrN3S/c16-11-4-3-5-12(10-11)20-14-7-9-18-15(19-14)13-6-1-2-8-17-13/h1-10H
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n/an/a 2.86E+3n/an/an/an/an/an/a



NPS Pharmaceuticals Inc

Curated by ChEMBL


Assay Description
Inhibition of glutamate-induced calcium influx in human mGluR5d by FLIPR


Bioorg Med Chem Lett 16: 2467-9 (2006)


Article DOI: 10.1016/j.bmcl.2006.01.100
BindingDB Entry DOI: 10.7270/Q22Z1544
More data for this
Ligand-Target Pair
Metabotropic glutamate receptor 5


(Homo sapiens (Human))
BDBM50182805
PNG
((4-chlorophenyl)(2-(pyridin-2-yl)pyrimidin-4-yl)me...)
Show SMILES OC(c1ccc(Cl)cc1)c1ccnc(n1)-c1ccccn1
Show InChI InChI=1S/C16H12ClN3O/c17-12-6-4-11(5-7-12)15(21)13-8-10-19-16(20-13)14-3-1-2-9-18-14/h1-10,15,21H
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n/an/a>3.00E+3n/an/an/an/an/an/a



NPS Pharmaceuticals Inc

Curated by ChEMBL


Assay Description
Inhibition of glutamate-induced calcium influx in human mGluR5d by FLIPR


Bioorg Med Chem Lett 16: 2467-9 (2006)


Article DOI: 10.1016/j.bmcl.2006.01.100
BindingDB Entry DOI: 10.7270/Q22Z1544
More data for this
Ligand-Target Pair
Cyclin-Dependent Kinase 5 (CDK5)


(Homo sapiens (Human))
BDBM50390640
PNG
(CHEMBL2069713)
Show SMILES NS(=O)(=O)c1cc(cs1)-c1nc2ccc(Cl)cc2s1
Show InChI InChI=1S/C11H7ClN2O2S3/c12-7-1-2-8-9(4-7)18-11(14-8)6-3-10(17-5-6)19(13,15)16/h1-5H,(H2,13,15,16)
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n/an/a 4.36E+3n/an/an/an/an/an/a



AstraZeneca

Curated by ChEMBL


Assay Description
Inhibition of Cdk5/p25-mediated myosin heavy chain phosphorylation in HEK293 cells


Bioorg Med Chem Lett 22: 5919-23 (2012)


Article DOI: 10.1016/j.bmcl.2012.07.068
BindingDB Entry DOI: 10.7270/Q2G73FTN
More data for this
Ligand-Target Pair
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