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Compile Data Set for Download or QSAR

Found 119 hits Enz. Inhib. hit(s) with all data for entry = 50016921   
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
Vascular endothelial growth factor receptor 2


(Homo sapiens (Human))
BDBM50175237
PNG
(CHEMBL199528 | N-butyl-N-methyl-3-phenyl-1H-thieno...)
Show SMILES CCCCN(C)C(=O)c1cc2c(n[nH]c2s1)-c1ccccc1
Show InChI InChI=1S/C17H19N3OS/c1-3-4-10-20(2)17(21)14-11-13-15(18-19-16(13)22-14)12-8-6-5-7-9-12/h5-9,11H,3-4,10H2,1-2H3,(H,18,19)
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n/an/a 350n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against KDR


Bioorg Med Chem Lett 16: 96-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.09.042
BindingDB Entry DOI: 10.7270/Q2JH3KRS
More data for this
Ligand-Target Pair
Vascular endothelial growth factor receptor 2


(Homo sapiens (Human))
BDBM50175239
PNG
(CHEMBL199755 | N-cyclohexyl-3-phenyl-1H-thieno[2,3...)
Show SMILES O=C(NC1CCCCC1)c1cc2c(n[nH]c2s1)-c1ccccc1
Show InChI InChI=1S/C18H19N3OS/c22-17(19-13-9-5-2-6-10-13)15-11-14-16(20-21-18(14)23-15)12-7-3-1-4-8-12/h1,3-4,7-8,11,13H,2,5-6,9-10H2,(H,19,22)(H,20,21)
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n/an/a 490n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against KDR


Bioorg Med Chem Lett 16: 96-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.09.042
BindingDB Entry DOI: 10.7270/Q2JH3KRS
More data for this
Ligand-Target Pair
Vascular endothelial growth factor receptor 2


(Homo sapiens (Human))
BDBM50175247
PNG
(CHEMBL200499 | N-benzyl-3-phenyl-1H-thieno[2,3-c]p...)
Show SMILES O=C(NCc1ccccc1)c1cc2c(n[nH]c2s1)-c1ccccc1
Show InChI InChI=1S/C19H15N3OS/c23-18(20-12-13-7-3-1-4-8-13)16-11-15-17(21-22-19(15)24-16)14-9-5-2-6-10-14/h1-11H,12H2,(H,20,23)(H,21,22)
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n/an/a 500n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against KDR


Bioorg Med Chem Lett 16: 96-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.09.042
BindingDB Entry DOI: 10.7270/Q2JH3KRS
More data for this
Ligand-Target Pair
Vascular endothelial growth factor receptor 2


(Homo sapiens (Human))
BDBM50175241
PNG
(CHEMBL199383 | N-(4-methoxybenzyl)-3-phenyl-1H-thi...)
Show SMILES COc1ccc(CNC(=O)c2cc3c(n[nH]c3s2)-c2ccccc2)cc1
Show InChI InChI=1S/C20H17N3O2S/c1-25-15-9-7-13(8-10-15)12-21-19(24)17-11-16-18(22-23-20(16)26-17)14-5-3-2-4-6-14/h2-11H,12H2,1H3,(H,21,24)(H,22,23)
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n/an/a 510n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against KDR


Bioorg Med Chem Lett 16: 96-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.09.042
BindingDB Entry DOI: 10.7270/Q2JH3KRS
More data for this
Ligand-Target Pair
Vascular endothelial growth factor receptor 2


(Homo sapiens (Human))
BDBM50175234
PNG
(CHEMBL197923 | N-phenethyl-3-phenyl-1H-thieno[2,3-...)
Show SMILES O=C(NCCc1ccccc1)c1cc2c(n[nH]c2s1)-c1ccccc1
Show InChI InChI=1S/C20H17N3OS/c24-19(21-12-11-14-7-3-1-4-8-14)17-13-16-18(22-23-20(16)25-17)15-9-5-2-6-10-15/h1-10,13H,11-12H2,(H,21,24)(H,22,23)
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n/an/a 2.00E+3n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against KDR


Bioorg Med Chem Lett 16: 96-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.09.042
BindingDB Entry DOI: 10.7270/Q2JH3KRS
More data for this
Ligand-Target Pair
Vascular endothelial growth factor receptor 2


(Homo sapiens (Human))
BDBM50175232
PNG
((4-methylpiperazin-1-yl)(3-phenyl-1H-thieno[2,3-c]...)
Show SMILES CN1CCN(CC1)C(=O)c1cc2c(n[nH]c2s1)-c1ccccc1
Show InChI InChI=1S/C17H18N4OS/c1-20-7-9-21(10-8-20)17(22)14-11-13-15(18-19-16(13)23-14)12-5-3-2-4-6-12/h2-6,11H,7-10H2,1H3,(H,18,19)
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n/an/a 4.00E+3n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against KDR


Bioorg Med Chem Lett 16: 96-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.09.042
BindingDB Entry DOI: 10.7270/Q2JH3KRS
More data for this
Ligand-Target Pair
Vascular endothelial growth factor receptor 2


(Homo sapiens (Human))
BDBM50175246
PNG
(3-methyl-4-(thiophene-2-carboxamido)-1H-thieno[2,3...)
Show SMILES Cc1[nH]nc2sc(C(N)=O)c(NC(=O)c3cccs3)c12
Show InChI InChI=1S/C12H10N4O2S2/c1-5-7-8(14-11(18)6-3-2-4-19-6)9(10(13)17)20-12(7)16-15-5/h2-4H,1H3,(H2,13,17)(H,14,18)(H,15,16)
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n/an/a 6.00E+3n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against KDR


Bioorg Med Chem Lett 16: 96-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.09.042
BindingDB Entry DOI: 10.7270/Q2JH3KRS
More data for this
Ligand-Target Pair
Vascular endothelial growth factor receptor 2


(Homo sapiens (Human))
BDBM50175235
PNG
(4-(2-chlorobenzamido)-3-methyl-1H-thieno[2,3-c]pyr...)
Show SMILES Cc1[nH]nc2sc(C(N)=O)c(NC(=O)c3ccccc3Cl)c12
Show InChI InChI=1S/C14H11ClN4O2S/c1-6-9-10(11(12(16)20)22-14(9)19-18-6)17-13(21)7-4-2-3-5-8(7)15/h2-5H,1H3,(H2,16,20)(H,17,21)(H,18,19)
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n/an/a 8.00E+3n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against KDR


Bioorg Med Chem Lett 16: 96-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.09.042
BindingDB Entry DOI: 10.7270/Q2JH3KRS
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase PLK1


(Homo sapiens (Human))
BDBM50175250
PNG
(CHEMBL370199 | methyl 2-(5-carbamoyl-3-methyl-1H-t...)
Show SMILES COC(=O)C(=O)Nc1c(sc2n[nH]c(C)c12)C(N)=O
Show InChI InChI=1S/C10H10N4O4S/c1-3-4-5(12-8(16)10(17)18-2)6(7(11)15)19-9(4)14-13-3/h1-2H3,(H2,11,15)(H,12,16)(H,13,14)
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n/an/a 8.00E+3n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against Plk1


Bioorg Med Chem Lett 16: 96-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.09.042
BindingDB Entry DOI: 10.7270/Q2JH3KRS
More data for this
Ligand-Target Pair
RAC-alpha serine/threonine-protein kinase


(Homo sapiens (Human))
BDBM50175245
PNG
(1-(5-carbamoyl-3-methyl-1H-thieno[2,3-c]pyrazol-4-...)
Show SMILES Cc1[nH]nc2sc(C(N)=O)c(NC(=O)Nc3ccccc3)c12
Show InChI InChI=1S/C14H13N5O2S/c1-7-9-10(11(12(15)20)22-13(9)19-18-7)17-14(21)16-8-5-3-2-4-6-8/h2-6H,1H3,(H2,15,20)(H,18,19)(H2,16,17,21)
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n/an/a 9.00E+3n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against Akt1


Bioorg Med Chem Lett 16: 96-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.09.042
BindingDB Entry DOI: 10.7270/Q2JH3KRS
More data for this
Ligand-Target Pair
Cyclin-A1/Cyclin-A2/Cyclin-dependent kinase 2


(Homo sapiens (Human))
BDBM50175239
PNG
(CHEMBL199755 | N-cyclohexyl-3-phenyl-1H-thieno[2,3...)
Show SMILES O=C(NC1CCCCC1)c1cc2c(n[nH]c2s1)-c1ccccc1
Show InChI InChI=1S/C18H19N3OS/c22-17(19-13-9-5-2-6-10-13)15-11-14-16(20-21-18(14)23-15)12-7-3-1-4-8-12/h1,3-4,7-8,11,13H,2,5-6,9-10H2,(H,19,22)(H,20,21)
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n/an/a 1.10E+4n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against CDK2/Cyclin A


Bioorg Med Chem Lett 16: 96-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.09.042
BindingDB Entry DOI: 10.7270/Q2JH3KRS
More data for this
Ligand-Target Pair
Vascular endothelial growth factor receptor 2


(Homo sapiens (Human))
BDBM50175252
PNG
(3-methyl-4-(2-phenoxyacetamido)-1H-thieno[2,3-c]py...)
Show SMILES Cc1[nH]nc2sc(C(N)=O)c(NC(=O)COc3ccccc3)c12
Show InChI InChI=1S/C15H14N4O3S/c1-8-11-12(13(14(16)21)23-15(11)19-18-8)17-10(20)7-22-9-5-3-2-4-6-9/h2-6H,7H2,1H3,(H2,16,21)(H,17,20)(H,18,19)
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n/an/a 1.10E+4n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against KDR


Bioorg Med Chem Lett 16: 96-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.09.042
BindingDB Entry DOI: 10.7270/Q2JH3KRS
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase PLK1


(Homo sapiens (Human))
BDBM50175239
PNG
(CHEMBL199755 | N-cyclohexyl-3-phenyl-1H-thieno[2,3...)
Show SMILES O=C(NC1CCCCC1)c1cc2c(n[nH]c2s1)-c1ccccc1
Show InChI InChI=1S/C18H19N3OS/c22-17(19-13-9-5-2-6-10-13)15-11-14-16(20-21-18(14)23-15)12-7-3-1-4-8-12/h1,3-4,7-8,11,13H,2,5-6,9-10H2,(H,19,22)(H,20,21)
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n/an/a 1.20E+4n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against Plk1


Bioorg Med Chem Lett 16: 96-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.09.042
BindingDB Entry DOI: 10.7270/Q2JH3KRS
More data for this
Ligand-Target Pair
Vascular endothelial growth factor receptor 2


(Homo sapiens (Human))
BDBM50175243
PNG
(CHEMBL373001 | N-benzyl-3-methyl-1H-thieno[2,3-c]p...)
Show SMILES Cc1n[nH]c2sc(cc12)C(=O)NCc1ccccc1
Show InChI InChI=1S/C14H13N3OS/c1-9-11-7-12(19-14(11)17-16-9)13(18)15-8-10-5-3-2-4-6-10/h2-7H,8H2,1H3,(H,15,18)(H,16,17)
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n/an/a 1.20E+4n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against KDR


Bioorg Med Chem Lett 16: 96-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.09.042
BindingDB Entry DOI: 10.7270/Q2JH3KRS
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase PAK 4


(Homo sapiens (Human))
BDBM50175245
PNG
(1-(5-carbamoyl-3-methyl-1H-thieno[2,3-c]pyrazol-4-...)
Show SMILES Cc1[nH]nc2sc(C(N)=O)c(NC(=O)Nc3ccccc3)c12
Show InChI InChI=1S/C14H13N5O2S/c1-7-9-10(11(12(15)20)22-13(9)19-18-7)17-14(21)16-8-5-3-2-4-6-8/h2-6H,1H3,(H2,15,20)(H,18,19)(H2,16,17,21)
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n/an/a 1.30E+4n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against Pak4


Bioorg Med Chem Lett 16: 96-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.09.042
BindingDB Entry DOI: 10.7270/Q2JH3KRS
More data for this
Ligand-Target Pair
RAC-alpha serine/threonine-protein kinase


(Homo sapiens (Human))
BDBM50175247
PNG
(CHEMBL200499 | N-benzyl-3-phenyl-1H-thieno[2,3-c]p...)
Show SMILES O=C(NCc1ccccc1)c1cc2c(n[nH]c2s1)-c1ccccc1
Show InChI InChI=1S/C19H15N3OS/c23-18(20-12-13-7-3-1-4-8-13)16-11-15-17(21-22-19(15)24-16)14-9-5-2-6-10-14/h1-11H,12H2,(H,20,23)(H,21,22)
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n/an/a 1.50E+4n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against Akt1


Bioorg Med Chem Lett 16: 96-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.09.042
BindingDB Entry DOI: 10.7270/Q2JH3KRS
More data for this
Ligand-Target Pair
RAC-alpha serine/threonine-protein kinase


(Homo sapiens (Human))
BDBM50175251
PNG
(CHEMBL200796 | methyl 3-(phenylamino)-1H-thieno[2,...)
Show SMILES COC(=O)c1cc2c(Nc3ccccc3)[nH]nc2s1
Show InChI InChI=1S/C13H11N3O2S/c1-18-13(17)10-7-9-11(15-16-12(9)19-10)14-8-5-3-2-4-6-8/h2-7H,1H3,(H2,14,15,16)
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n/an/a 1.60E+4n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against Akt1


Bioorg Med Chem Lett 16: 96-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.09.042
BindingDB Entry DOI: 10.7270/Q2JH3KRS
More data for this
Ligand-Target Pair
Vascular endothelial growth factor receptor 2


(Homo sapiens (Human))
BDBM50175249
PNG
(CHEMBL371242 | N-butyl-3-methyl-1H-thieno[2,3-c]py...)
Show SMILES CCCCNC(=O)c1cc2c(C)n[nH]c2s1
Show InChI InChI=1S/C11H15N3OS/c1-3-4-5-12-10(15)9-6-8-7(2)13-14-11(8)16-9/h6H,3-5H2,1-2H3,(H,12,15)(H,13,14)
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n/an/a 1.60E+4n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against KDR


Bioorg Med Chem Lett 16: 96-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.09.042
BindingDB Entry DOI: 10.7270/Q2JH3KRS
More data for this
Ligand-Target Pair
MAP kinase-activated protein kinase 2


(Homo sapiens (Human))
BDBM50175241
PNG
(CHEMBL199383 | N-(4-methoxybenzyl)-3-phenyl-1H-thi...)
Show SMILES COc1ccc(CNC(=O)c2cc3c(n[nH]c3s2)-c2ccccc2)cc1
Show InChI InChI=1S/C20H17N3O2S/c1-25-15-9-7-13(8-10-15)12-21-19(24)17-11-16-18(22-23-20(16)26-17)14-5-3-2-4-6-14/h2-11H,12H2,1H3,(H,21,24)(H,22,23)
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n/an/a 1.60E+4n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against MK2


Bioorg Med Chem Lett 16: 96-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.09.042
BindingDB Entry DOI: 10.7270/Q2JH3KRS
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase PLK1


(Homo sapiens (Human))
BDBM50175243
PNG
(CHEMBL373001 | N-benzyl-3-methyl-1H-thieno[2,3-c]p...)
Show SMILES Cc1n[nH]c2sc(cc12)C(=O)NCc1ccccc1
Show InChI InChI=1S/C14H13N3OS/c1-9-11-7-12(19-14(11)17-16-9)13(18)15-8-10-5-3-2-4-6-10/h2-7H,8H2,1H3,(H,15,18)(H,16,17)
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n/an/a 1.60E+4n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against Plk1


Bioorg Med Chem Lett 16: 96-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.09.042
BindingDB Entry DOI: 10.7270/Q2JH3KRS
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase PLK1


(Homo sapiens (Human))
BDBM50175234
PNG
(CHEMBL197923 | N-phenethyl-3-phenyl-1H-thieno[2,3-...)
Show SMILES O=C(NCCc1ccccc1)c1cc2c(n[nH]c2s1)-c1ccccc1
Show InChI InChI=1S/C20H17N3OS/c24-19(21-12-11-14-7-3-1-4-8-14)17-13-16-18(22-23-20(16)25-17)15-9-5-2-6-10-15/h1-10,13H,11-12H2,(H,21,24)(H,22,23)
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n/an/a 1.70E+4n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against Plk1


Bioorg Med Chem Lett 16: 96-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.09.042
BindingDB Entry DOI: 10.7270/Q2JH3KRS
More data for this
Ligand-Target Pair
Vascular endothelial growth factor receptor 2


(Homo sapiens (Human))
BDBM50175250
PNG
(CHEMBL370199 | methyl 2-(5-carbamoyl-3-methyl-1H-t...)
Show SMILES COC(=O)C(=O)Nc1c(sc2n[nH]c(C)c12)C(N)=O
Show InChI InChI=1S/C10H10N4O4S/c1-3-4-5(12-8(16)10(17)18-2)6(7(11)15)19-9(4)14-13-3/h1-2H3,(H2,11,15)(H,12,16)(H,13,14)
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n/an/a 1.70E+4n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against KDR


Bioorg Med Chem Lett 16: 96-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.09.042
BindingDB Entry DOI: 10.7270/Q2JH3KRS
More data for this
Ligand-Target Pair
Vascular endothelial growth factor receptor 2


(Homo sapiens (Human))
BDBM50175238
PNG
(3-methyl-1H-thieno[2,3-c]pyrazole-5-carboxamide | ...)
Show SMILES Cc1n[nH]c2sc(cc12)C(N)=O
Show InChI InChI=1S/C7H7N3OS/c1-3-4-2-5(6(8)11)12-7(4)10-9-3/h2H,1H3,(H2,8,11)(H,9,10)
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n/an/a 1.70E+4n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against KDR


Bioorg Med Chem Lett 16: 96-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.09.042
BindingDB Entry DOI: 10.7270/Q2JH3KRS
More data for this
Ligand-Target Pair
MAP kinase-activated protein kinase 2


(Homo sapiens (Human))
BDBM50175247
PNG
(CHEMBL200499 | N-benzyl-3-phenyl-1H-thieno[2,3-c]p...)
Show SMILES O=C(NCc1ccccc1)c1cc2c(n[nH]c2s1)-c1ccccc1
Show InChI InChI=1S/C19H15N3OS/c23-18(20-12-13-7-3-1-4-8-13)16-11-15-17(21-22-19(15)24-16)14-9-5-2-6-10-14/h1-11H,12H2,(H,20,23)(H,21,22)
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n/an/a 1.70E+4n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against MK2


Bioorg Med Chem Lett 16: 96-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.09.042
BindingDB Entry DOI: 10.7270/Q2JH3KRS
More data for this
Ligand-Target Pair
RAC-alpha serine/threonine-protein kinase


(Homo sapiens (Human))
BDBM50175246
PNG
(3-methyl-4-(thiophene-2-carboxamido)-1H-thieno[2,3...)
Show SMILES Cc1[nH]nc2sc(C(N)=O)c(NC(=O)c3cccs3)c12
Show InChI InChI=1S/C12H10N4O2S2/c1-5-7-8(14-11(18)6-3-2-4-19-6)9(10(13)17)20-12(7)16-15-5/h2-4H,1H3,(H2,13,17)(H,14,18)(H,15,16)
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n/an/a 1.70E+4n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against Akt1


Bioorg Med Chem Lett 16: 96-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.09.042
BindingDB Entry DOI: 10.7270/Q2JH3KRS
More data for this
Ligand-Target Pair
Vascular endothelial growth factor receptor 2


(Homo sapiens (Human))
BDBM50175236
PNG
(4-acetamido-3-methyl-1H-thieno[2,3-c]pyrazole-5-ca...)
Show SMILES CC(=O)Nc1c(sc2n[nH]c(C)c12)C(N)=O
Show InChI InChI=1S/C9H10N4O2S/c1-3-5-6(11-4(2)14)7(8(10)15)16-9(5)13-12-3/h1-2H3,(H2,10,15)(H,11,14)(H,12,13)
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n/an/a 1.90E+4n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against KDR


Bioorg Med Chem Lett 16: 96-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.09.042
BindingDB Entry DOI: 10.7270/Q2JH3KRS
More data for this
Ligand-Target Pair
Cyclin-A1/Cyclin-A2/Cyclin-dependent kinase 2


(Homo sapiens (Human))
BDBM50175237
PNG
(CHEMBL199528 | N-butyl-N-methyl-3-phenyl-1H-thieno...)
Show SMILES CCCCN(C)C(=O)c1cc2c(n[nH]c2s1)-c1ccccc1
Show InChI InChI=1S/C17H19N3OS/c1-3-4-10-20(2)17(21)14-11-13-15(18-19-16(13)22-14)12-8-6-5-7-9-12/h5-9,11H,3-4,10H2,1-2H3,(H,18,19)
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n/an/a>2.00E+4n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against CDK2/Cyclin A


Bioorg Med Chem Lett 16: 96-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.09.042
BindingDB Entry DOI: 10.7270/Q2JH3KRS
More data for this
Ligand-Target Pair
Cyclin-A1/Cyclin-A2/Cyclin-dependent kinase 2


(Homo sapiens (Human))
BDBM50175232
PNG
((4-methylpiperazin-1-yl)(3-phenyl-1H-thieno[2,3-c]...)
Show SMILES CN1CCN(CC1)C(=O)c1cc2c(n[nH]c2s1)-c1ccccc1
Show InChI InChI=1S/C17H18N4OS/c1-20-7-9-21(10-8-20)17(22)14-11-13-15(18-19-16(13)23-14)12-5-3-2-4-6-12/h2-6,11H,7-10H2,1H3,(H,18,19)
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n/an/a>2.00E+4n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against CDK2/Cyclin A


Bioorg Med Chem Lett 16: 96-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.09.042
BindingDB Entry DOI: 10.7270/Q2JH3KRS
More data for this
Ligand-Target Pair
Cyclin-A1/Cyclin-A2/Cyclin-dependent kinase 2


(Homo sapiens (Human))
BDBM50175234
PNG
(CHEMBL197923 | N-phenethyl-3-phenyl-1H-thieno[2,3-...)
Show SMILES O=C(NCCc1ccccc1)c1cc2c(n[nH]c2s1)-c1ccccc1
Show InChI InChI=1S/C20H17N3OS/c24-19(21-12-11-14-7-3-1-4-8-14)17-13-16-18(22-23-20(16)25-17)15-9-5-2-6-10-15/h1-10,13H,11-12H2,(H,21,24)(H,22,23)
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n/an/a>2.00E+4n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against CDK2/Cyclin A


Bioorg Med Chem Lett 16: 96-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.09.042
BindingDB Entry DOI: 10.7270/Q2JH3KRS
More data for this
Ligand-Target Pair
Cyclin-A1/Cyclin-A2/Cyclin-dependent kinase 2


(Homo sapiens (Human))
BDBM50175241
PNG
(CHEMBL199383 | N-(4-methoxybenzyl)-3-phenyl-1H-thi...)
Show SMILES COc1ccc(CNC(=O)c2cc3c(n[nH]c3s2)-c2ccccc2)cc1
Show InChI InChI=1S/C20H17N3O2S/c1-25-15-9-7-13(8-10-15)12-21-19(24)17-11-16-18(22-23-20(16)26-17)14-5-3-2-4-6-14/h2-11H,12H2,1H3,(H,21,24)(H,22,23)
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n/an/a>2.00E+4n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against CDK2/Cyclin A


Bioorg Med Chem Lett 16: 96-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.09.042
BindingDB Entry DOI: 10.7270/Q2JH3KRS
More data for this
Ligand-Target Pair
Mitogen-activated protein kinase kinase kinase 8


(Homo sapiens (Human))
BDBM50175232
PNG
((4-methylpiperazin-1-yl)(3-phenyl-1H-thieno[2,3-c]...)
Show SMILES CN1CCN(CC1)C(=O)c1cc2c(n[nH]c2s1)-c1ccccc1
Show InChI InChI=1S/C17H18N4OS/c1-20-7-9-21(10-8-20)17(22)14-11-13-15(18-19-16(13)23-14)12-5-3-2-4-6-12/h2-6,11H,7-10H2,1H3,(H,18,19)
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n/an/a>2.00E+4n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against COT


Bioorg Med Chem Lett 16: 96-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.09.042
BindingDB Entry DOI: 10.7270/Q2JH3KRS
More data for this
Ligand-Target Pair
Mitogen-activated protein kinase kinase kinase 8


(Homo sapiens (Human))
BDBM50175234
PNG
(CHEMBL197923 | N-phenethyl-3-phenyl-1H-thieno[2,3-...)
Show SMILES O=C(NCCc1ccccc1)c1cc2c(n[nH]c2s1)-c1ccccc1
Show InChI InChI=1S/C20H17N3OS/c24-19(21-12-11-14-7-3-1-4-8-14)17-13-16-18(22-23-20(16)25-17)15-9-5-2-6-10-15/h1-10,13H,11-12H2,(H,21,24)(H,22,23)
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n/an/a>2.00E+4n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against COT


Bioorg Med Chem Lett 16: 96-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.09.042
BindingDB Entry DOI: 10.7270/Q2JH3KRS
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase PAK 4


(Homo sapiens (Human))
BDBM50175238
PNG
(3-methyl-1H-thieno[2,3-c]pyrazole-5-carboxamide | ...)
Show SMILES Cc1n[nH]c2sc(cc12)C(N)=O
Show InChI InChI=1S/C7H7N3OS/c1-3-4-2-5(6(8)11)12-7(4)10-9-3/h2H,1H3,(H2,8,11)(H,9,10)
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n/an/a>2.00E+4n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against Pak4


Bioorg Med Chem Lett 16: 96-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.09.042
BindingDB Entry DOI: 10.7270/Q2JH3KRS
More data for this
Ligand-Target Pair
Mitogen-activated protein kinase kinase kinase 8


(Homo sapiens (Human))
BDBM50175239
PNG
(CHEMBL199755 | N-cyclohexyl-3-phenyl-1H-thieno[2,3...)
Show SMILES O=C(NC1CCCCC1)c1cc2c(n[nH]c2s1)-c1ccccc1
Show InChI InChI=1S/C18H19N3OS/c22-17(19-13-9-5-2-6-10-13)15-11-14-16(20-21-18(14)23-15)12-7-3-1-4-8-12/h1,3-4,7-8,11,13H,2,5-6,9-10H2,(H,19,22)(H,20,21)
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n/an/a>2.00E+4n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against COT


Bioorg Med Chem Lett 16: 96-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.09.042
BindingDB Entry DOI: 10.7270/Q2JH3KRS
More data for this
Ligand-Target Pair
Mitogen-activated protein kinase kinase kinase 8


(Homo sapiens (Human))
BDBM50175240
PNG
(CHEMBL199951 | N-cyclohexyl-3-methyl-1H-thieno[2,3...)
Show SMILES Cc1n[nH]c2sc(cc12)C(=O)NC1CCCCC1
Show InChI InChI=1S/C13H17N3OS/c1-8-10-7-11(18-13(10)16-15-8)12(17)14-9-5-3-2-4-6-9/h7,9H,2-6H2,1H3,(H,14,17)(H,15,16)
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n/an/a>2.00E+4n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against COT


Bioorg Med Chem Lett 16: 96-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.09.042
BindingDB Entry DOI: 10.7270/Q2JH3KRS
More data for this
Ligand-Target Pair
MAP kinase-activated protein kinase 2


(Homo sapiens (Human))
BDBM50175243
PNG
(CHEMBL373001 | N-benzyl-3-methyl-1H-thieno[2,3-c]p...)
Show SMILES Cc1n[nH]c2sc(cc12)C(=O)NCc1ccccc1
Show InChI InChI=1S/C14H13N3OS/c1-9-11-7-12(19-14(11)17-16-9)13(18)15-8-10-5-3-2-4-6-10/h2-7H,8H2,1H3,(H,15,18)(H,16,17)
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n/an/a>2.00E+4n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against MK2


Bioorg Med Chem Lett 16: 96-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.09.042
BindingDB Entry DOI: 10.7270/Q2JH3KRS
More data for this
Ligand-Target Pair
Mitogen-activated protein kinase 14


(Homo sapiens (Human))
BDBM50175232
PNG
((4-methylpiperazin-1-yl)(3-phenyl-1H-thieno[2,3-c]...)
Show SMILES CN1CCN(CC1)C(=O)c1cc2c(n[nH]c2s1)-c1ccccc1
Show InChI InChI=1S/C17H18N4OS/c1-20-7-9-21(10-8-20)17(22)14-11-13-15(18-19-16(13)23-14)12-5-3-2-4-6-12/h2-6,11H,7-10H2,1H3,(H,18,19)
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n/an/a>2.00E+4n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against p38alpha


Bioorg Med Chem Lett 16: 96-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.09.042
BindingDB Entry DOI: 10.7270/Q2JH3KRS
More data for this
Ligand-Target Pair
Vascular endothelial growth factor receptor 2


(Homo sapiens (Human))
BDBM50175242
PNG
(CHEMBL200657 | N-butyl-N,3-dimethyl-1H-thieno[2,3-...)
Show SMILES CCCCN(C)C(=O)c1cc2c(C)n[nH]c2s1
Show InChI InChI=1S/C12H17N3OS/c1-4-5-6-15(3)12(16)10-7-9-8(2)13-14-11(9)17-10/h7H,4-6H2,1-3H3,(H,13,14)
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Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against KDR


Bioorg Med Chem Lett 16: 96-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.09.042
BindingDB Entry DOI: 10.7270/Q2JH3KRS
More data for this
Ligand-Target Pair
MAP kinase-activated protein kinase 2


(Homo sapiens (Human))
BDBM50175234
PNG
(CHEMBL197923 | N-phenethyl-3-phenyl-1H-thieno[2,3-...)
Show SMILES O=C(NCCc1ccccc1)c1cc2c(n[nH]c2s1)-c1ccccc1
Show InChI InChI=1S/C20H17N3OS/c24-19(21-12-11-14-7-3-1-4-8-14)17-13-16-18(22-23-20(16)25-17)15-9-5-2-6-10-15/h1-10,13H,11-12H2,(H,21,24)(H,22,23)
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Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against MK2


Bioorg Med Chem Lett 16: 96-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.09.042
BindingDB Entry DOI: 10.7270/Q2JH3KRS
More data for this
Ligand-Target Pair
RAC-alpha serine/threonine-protein kinase


(Homo sapiens (Human))
BDBM50175243
PNG
(CHEMBL373001 | N-benzyl-3-methyl-1H-thieno[2,3-c]p...)
Show SMILES Cc1n[nH]c2sc(cc12)C(=O)NCc1ccccc1
Show InChI InChI=1S/C14H13N3OS/c1-9-11-7-12(19-14(11)17-16-9)13(18)15-8-10-5-3-2-4-6-10/h2-7H,8H2,1H3,(H,15,18)(H,16,17)
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n/an/a>2.00E+4n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against Akt1


Bioorg Med Chem Lett 16: 96-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.09.042
BindingDB Entry DOI: 10.7270/Q2JH3KRS
More data for this
Ligand-Target Pair
Mitogen-activated protein kinase 14


(Homo sapiens (Human))
BDBM50175239
PNG
(CHEMBL199755 | N-cyclohexyl-3-phenyl-1H-thieno[2,3...)
Show SMILES O=C(NC1CCCCC1)c1cc2c(n[nH]c2s1)-c1ccccc1
Show InChI InChI=1S/C18H19N3OS/c22-17(19-13-9-5-2-6-10-13)15-11-14-16(20-21-18(14)23-15)12-7-3-1-4-8-12/h1,3-4,7-8,11,13H,2,5-6,9-10H2,(H,19,22)(H,20,21)
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n/an/a>2.00E+4n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against p38alpha


Bioorg Med Chem Lett 16: 96-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.09.042
BindingDB Entry DOI: 10.7270/Q2JH3KRS
More data for this
Ligand-Target Pair
Mitogen-activated protein kinase 14


(Homo sapiens (Human))
BDBM50175237
PNG
(CHEMBL199528 | N-butyl-N-methyl-3-phenyl-1H-thieno...)
Show SMILES CCCCN(C)C(=O)c1cc2c(n[nH]c2s1)-c1ccccc1
Show InChI InChI=1S/C17H19N3OS/c1-3-4-10-20(2)17(21)14-11-13-15(18-19-16(13)22-14)12-8-6-5-7-9-12/h5-9,11H,3-4,10H2,1-2H3,(H,18,19)
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n/an/a>2.00E+4n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against p38alpha


Bioorg Med Chem Lett 16: 96-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.09.042
BindingDB Entry DOI: 10.7270/Q2JH3KRS
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase PLK1


(Homo sapiens (Human))
BDBM50175236
PNG
(4-acetamido-3-methyl-1H-thieno[2,3-c]pyrazole-5-ca...)
Show SMILES CC(=O)Nc1c(sc2n[nH]c(C)c12)C(N)=O
Show InChI InChI=1S/C9H10N4O2S/c1-3-5-6(11-4(2)14)7(8(10)15)16-9(5)13-12-3/h1-2H3,(H2,10,15)(H,11,14)(H,12,13)
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n/an/a>2.00E+4n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against Plk1


Bioorg Med Chem Lett 16: 96-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.09.042
BindingDB Entry DOI: 10.7270/Q2JH3KRS
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase PAK 4


(Homo sapiens (Human))
BDBM50175232
PNG
((4-methylpiperazin-1-yl)(3-phenyl-1H-thieno[2,3-c]...)
Show SMILES CN1CCN(CC1)C(=O)c1cc2c(n[nH]c2s1)-c1ccccc1
Show InChI InChI=1S/C17H18N4OS/c1-20-7-9-21(10-8-20)17(22)14-11-13-15(18-19-16(13)23-14)12-5-3-2-4-6-12/h2-6,11H,7-10H2,1H3,(H,18,19)
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n/an/a>2.00E+4n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against Pak4


Bioorg Med Chem Lett 16: 96-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.09.042
BindingDB Entry DOI: 10.7270/Q2JH3KRS
More data for this
Ligand-Target Pair
Mitogen-activated protein kinase kinase kinase 8


(Homo sapiens (Human))
BDBM50175242
PNG
(CHEMBL200657 | N-butyl-N,3-dimethyl-1H-thieno[2,3-...)
Show SMILES CCCCN(C)C(=O)c1cc2c(C)n[nH]c2s1
Show InChI InChI=1S/C12H17N3OS/c1-4-5-6-15(3)12(16)10-7-9-8(2)13-14-11(9)17-10/h7H,4-6H2,1-3H3,(H,13,14)
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n/an/a>2.00E+4n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against COT


Bioorg Med Chem Lett 16: 96-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.09.042
BindingDB Entry DOI: 10.7270/Q2JH3KRS
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase PAK 4


(Homo sapiens (Human))
BDBM50175249
PNG
(CHEMBL371242 | N-butyl-3-methyl-1H-thieno[2,3-c]py...)
Show SMILES CCCCNC(=O)c1cc2c(C)n[nH]c2s1
Show InChI InChI=1S/C11H15N3OS/c1-3-4-5-12-10(15)9-6-8-7(2)13-14-11(8)16-9/h6H,3-5H2,1-2H3,(H,12,15)(H,13,14)
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n/an/a>2.00E+4n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against Pak4


Bioorg Med Chem Lett 16: 96-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.09.042
BindingDB Entry DOI: 10.7270/Q2JH3KRS
More data for this
Ligand-Target Pair
RAC-alpha serine/threonine-protein kinase


(Homo sapiens (Human))
BDBM50175249
PNG
(CHEMBL371242 | N-butyl-3-methyl-1H-thieno[2,3-c]py...)
Show SMILES CCCCNC(=O)c1cc2c(C)n[nH]c2s1
Show InChI InChI=1S/C11H15N3OS/c1-3-4-5-12-10(15)9-6-8-7(2)13-14-11(8)16-9/h6H,3-5H2,1-2H3,(H,12,15)(H,13,14)
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n/an/a>2.00E+4n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against Akt1


Bioorg Med Chem Lett 16: 96-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.09.042
BindingDB Entry DOI: 10.7270/Q2JH3KRS
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase PAK 4


(Homo sapiens (Human))
BDBM50175240
PNG
(CHEMBL199951 | N-cyclohexyl-3-methyl-1H-thieno[2,3...)
Show SMILES Cc1n[nH]c2sc(cc12)C(=O)NC1CCCCC1
Show InChI InChI=1S/C13H17N3OS/c1-8-10-7-11(18-13(10)16-15-8)12(17)14-9-5-3-2-4-6-9/h7,9H,2-6H2,1H3,(H,14,17)(H,15,16)
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n/an/a>2.00E+4n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against Pak4


Bioorg Med Chem Lett 16: 96-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.09.042
BindingDB Entry DOI: 10.7270/Q2JH3KRS
More data for this
Ligand-Target Pair
RAC-alpha serine/threonine-protein kinase


(Homo sapiens (Human))
BDBM50175240
PNG
(CHEMBL199951 | N-cyclohexyl-3-methyl-1H-thieno[2,3...)
Show SMILES Cc1n[nH]c2sc(cc12)C(=O)NC1CCCCC1
Show InChI InChI=1S/C13H17N3OS/c1-8-10-7-11(18-13(10)16-15-8)12(17)14-9-5-3-2-4-6-9/h7,9H,2-6H2,1H3,(H,14,17)(H,15,16)
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n/an/a>2.00E+4n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against Akt1


Bioorg Med Chem Lett 16: 96-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.09.042
BindingDB Entry DOI: 10.7270/Q2JH3KRS
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase PLK1


(Homo sapiens (Human))
BDBM50175237
PNG
(CHEMBL199528 | N-butyl-N-methyl-3-phenyl-1H-thieno...)
Show SMILES CCCCN(C)C(=O)c1cc2c(n[nH]c2s1)-c1ccccc1
Show InChI InChI=1S/C17H19N3OS/c1-3-4-10-20(2)17(21)14-11-13-15(18-19-16(13)22-14)12-8-6-5-7-9-12/h5-9,11H,3-4,10H2,1-2H3,(H,18,19)
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n/an/a>2.00E+4n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against Plk1


Bioorg Med Chem Lett 16: 96-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.09.042
BindingDB Entry DOI: 10.7270/Q2JH3KRS
More data for this
Ligand-Target Pair
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