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32 similar compounds to monomer 50311932

Compile data set for download or QSAR
Wt: 583.5
BDBM50311889
Wt: 548.6
BDBM50311890
Wt: 576.7
BDBM50311891
Wt: 643.7
BDBM50311893
Wt: 547.5
BDBM50311894
Wt: 561.5
BDBM50311895
Wt: 503.4
BDBM50311901
Wt: 589.7
BDBM50311908
Wt: 602.6
BDBM50311909
Wt: 630.7
BDBM50311910
Wt: 629.6
BDBM50311911
Wt: 503.4
BDBM50311917
Wt: 643.7
BDBM50311912
Wt: 556.5
BDBM50311913
Wt: 469.9
BDBM50311916
Displayed 1 to 15 (of 32 total )  |  Next  |  Last  >>

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 114 hits for monomerid = 50311889,50311890,50311891,50311893,50311894,50311895,50311901,50311908,50311909,50311910,50311911,50311917,50311912,50311913,50311916   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kcal/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50311893
PNG
(CHEMBL1076478 | N-(4-methyl-3-(1-(6-(3-(4-methylpi...)
Show SMILES CN1CCN(CCCNc2cc(ncn2)-n2c(Nc3cc(NC(=O)c4cccc(c4)C(F)(F)F)ccc3C)nc3ccccc23)CC1
Show InChI InChI=1S/C34H36F3N9O/c1-23-11-12-26(41-32(47)24-7-5-8-25(19-24)34(35,36)37)20-28(23)43-33-42-27-9-3-4-10-29(27)46(33)31-21-30(39-22-40-31)38-13-6-14-45-17-15-44(2)16-18-45/h3-5,7-12,19-22H,6,13-18H2,1-2H3,(H,41,47)(H,42,43)(H,38,39,40)
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n/an/a 6n/an/an/an/an/an/a



Genomics Institute of the Novartis Research Foundation (GNF)

Curated by ChEMBL


Assay Description
Inhibition of LCK


Bioorg Med Chem Lett 19: 6691-5 (2009)


Article DOI: 10.1016/j.bmcl.2009.09.123
BindingDB Entry DOI: 10.7270/Q2Q52PRR
More data for this
Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))
BDBM50311895
PNG
(CHEMBL1076480 | N-(3-(1-(6-(2-methoxyethylamino)py...)
Show SMILES COCCNc1cc(ncn1)-n1c(Nc2cc(NC(=O)c3cccc(c3)C(F)(F)F)ccc2C)nc2ccccc12
Show InChI InChI=1S/C29H26F3N7O2/c1-18-10-11-21(36-27(40)19-6-5-7-20(14-19)29(30,31)32)15-23(18)38-28-37-22-8-3-4-9-24(22)39(28)26-16-25(34-17-35-26)33-12-13-41-2/h3-11,14-17H,12-13H2,1-2H3,(H,36,40)(H,37,38)(H,33,34,35)
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n/an/a 1.69E+3n/an/an/an/an/an/a



Genomics Institute of the Novartis Research Foundation (GNF)

Curated by ChEMBL


Assay Description
Inhibition of SRC


Bioorg Med Chem Lett 19: 6691-5 (2009)


Article DOI: 10.1016/j.bmcl.2009.09.123
BindingDB Entry DOI: 10.7270/Q2Q52PRR
More data for this
Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))
BDBM50311894
PNG
(CHEMBL1087638 | N-(3-(1-(6-(2-hydroxyethylamino)py...)
Show SMILES Cc1ccc(NC(=O)c2cccc(c2)C(F)(F)F)cc1Nc1nc2ccccc2n1-c1cc(NCCO)ncn1
Show InChI InChI=1S/C28H24F3N7O2/c1-17-9-10-20(35-26(40)18-5-4-6-19(13-18)28(29,30)31)14-22(17)37-27-36-21-7-2-3-8-23(21)38(27)25-15-24(32-11-12-39)33-16-34-25/h2-10,13-16,39H,11-12H2,1H3,(H,35,40)(H,36,37)(H,32,33,34)
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n/an/a 1.92E+3n/an/an/an/an/an/a



Genomics Institute of the Novartis Research Foundation (GNF)

Curated by ChEMBL


Assay Description
Inhibition of SRC


Bioorg Med Chem Lett 19: 6691-5 (2009)


Article DOI: 10.1016/j.bmcl.2009.09.123
BindingDB Entry DOI: 10.7270/Q2Q52PRR
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50311894
PNG
(CHEMBL1087638 | N-(3-(1-(6-(2-hydroxyethylamino)py...)
Show SMILES Cc1ccc(NC(=O)c2cccc(c2)C(F)(F)F)cc1Nc1nc2ccccc2n1-c1cc(NCCO)ncn1
Show InChI InChI=1S/C28H24F3N7O2/c1-17-9-10-20(35-26(40)18-5-4-6-19(13-18)28(29,30)31)14-22(17)37-27-36-21-7-2-3-8-23(21)38(27)25-15-24(32-11-12-39)33-16-34-25/h2-10,13-16,39H,11-12H2,1H3,(H,35,40)(H,36,37)(H,32,33,34)
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n/an/a 27n/an/an/an/an/an/a



Genomics Institute of the Novartis Research Foundation (GNF)

Curated by ChEMBL


Assay Description
Inhibition of LCK


Bioorg Med Chem Lett 19: 6691-5 (2009)


Article DOI: 10.1016/j.bmcl.2009.09.123
BindingDB Entry DOI: 10.7270/Q2Q52PRR
More data for this
Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))
BDBM50311893
PNG
(CHEMBL1076478 | N-(4-methyl-3-(1-(6-(3-(4-methylpi...)
Show SMILES CN1CCN(CCCNc2cc(ncn2)-n2c(Nc3cc(NC(=O)c4cccc(c4)C(F)(F)F)ccc3C)nc3ccccc23)CC1
Show InChI InChI=1S/C34H36F3N9O/c1-23-11-12-26(41-32(47)24-7-5-8-25(19-24)34(35,36)37)20-28(23)43-33-42-27-9-3-4-10-29(27)46(33)31-21-30(39-22-40-31)38-13-6-14-45-17-15-44(2)16-18-45/h3-5,7-12,19-22H,6,13-18H2,1-2H3,(H,41,47)(H,42,43)(H,38,39,40)
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n/an/a 601n/an/an/an/an/an/a



Genomics Institute of the Novartis Research Foundation (GNF)

Curated by ChEMBL


Assay Description
Inhibition of Tel-fused SRC expressed in mouse BAF3 cells


Bioorg Med Chem Lett 19: 6691-5 (2009)


Article DOI: 10.1016/j.bmcl.2009.09.123
BindingDB Entry DOI: 10.7270/Q2Q52PRR
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50311917
PNG
(CHEMBL1079945 | N-(3-(1-(6-aminopyrimidin-4-yl)-1H...)
Show SMILES Cc1ccc(NC(=O)c2cccc(c2)C(F)(F)F)cc1Nc1nc2ccccc2n1-c1cc(N)ncn1
Show InChI InChI=1S/C26H20F3N7O/c1-15-9-10-18(33-24(37)16-5-4-6-17(11-16)26(27,28)29)12-20(15)35-25-34-19-7-2-3-8-21(19)36(25)23-13-22(30)31-14-32-23/h2-14H,1H3,(H,33,37)(H,34,35)(H2,30,31,32)
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n/an/a 11n/an/an/an/an/an/a



Genomics Institute of the Novartis Research Foundation (GNF)

Curated by ChEMBL


Assay Description
Inhibition of LCK


Bioorg Med Chem Lett 19: 6691-5 (2009)


Article DOI: 10.1016/j.bmcl.2009.09.123
BindingDB Entry DOI: 10.7270/Q2Q52PRR
More data for this
Ligand-Target Pair
Insulin receptor


(Homo sapiens (Human))
BDBM50311917
PNG
(CHEMBL1079945 | N-(3-(1-(6-aminopyrimidin-4-yl)-1H...)
Show SMILES Cc1ccc(NC(=O)c2cccc(c2)C(F)(F)F)cc1Nc1nc2ccccc2n1-c1cc(N)ncn1
Show InChI InChI=1S/C26H20F3N7O/c1-15-9-10-18(33-24(37)16-5-4-6-17(11-16)26(27,28)29)12-20(15)35-25-34-19-7-2-3-8-21(19)36(25)23-13-22(30)31-14-32-23/h2-14H,1H3,(H,33,37)(H,34,35)(H2,30,31,32)
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n/an/a 661n/an/an/an/an/an/a



Genomics Institute of the Novartis Research Foundation (GNF)

Curated by ChEMBL


Assay Description
Inhibition of Tel-fused InsR expressed in mouse BAF3 cells


Bioorg Med Chem Lett 19: 6691-5 (2009)


Article DOI: 10.1016/j.bmcl.2009.09.123
BindingDB Entry DOI: 10.7270/Q2Q52PRR
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50311895
PNG
(CHEMBL1076480 | N-(3-(1-(6-(2-methoxyethylamino)py...)
Show SMILES COCCNc1cc(ncn1)-n1c(Nc2cc(NC(=O)c3cccc(c3)C(F)(F)F)ccc2C)nc2ccccc12
Show InChI InChI=1S/C29H26F3N7O2/c1-18-10-11-21(36-27(40)19-6-5-7-20(14-19)29(30,31)32)15-23(18)38-28-37-22-8-3-4-9-24(22)39(28)26-16-25(34-17-35-26)33-12-13-41-2/h3-11,14-17H,12-13H2,1-2H3,(H,36,40)(H,37,38)(H,33,34,35)
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n/an/a 135n/an/an/an/an/an/a



Genomics Institute of the Novartis Research Foundation (GNF)

Curated by ChEMBL


Assay Description
Inhibition of LCK


Bioorg Med Chem Lett 19: 6691-5 (2009)


Article DOI: 10.1016/j.bmcl.2009.09.123
BindingDB Entry DOI: 10.7270/Q2Q52PRR
More data for this
Ligand-Target Pair
Insulin receptor


(Homo sapiens (Human))
BDBM50311894
PNG
(CHEMBL1087638 | N-(3-(1-(6-(2-hydroxyethylamino)py...)
Show SMILES Cc1ccc(NC(=O)c2cccc(c2)C(F)(F)F)cc1Nc1nc2ccccc2n1-c1cc(NCCO)ncn1
Show InChI InChI=1S/C28H24F3N7O2/c1-17-9-10-20(35-26(40)18-5-4-6-19(13-18)28(29,30)31)14-22(17)37-27-36-21-7-2-3-8-23(21)38(27)25-15-24(32-11-12-39)33-16-34-25/h2-10,13-16,39H,11-12H2,1H3,(H,35,40)(H,36,37)(H,32,33,34)
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n/an/a 4.40E+3n/an/an/an/an/an/a



Genomics Institute of the Novartis Research Foundation (GNF)

Curated by ChEMBL


Assay Description
Inhibition of Tel-fused InsR expressed in mouse BAF3 cells


Bioorg Med Chem Lett 19: 6691-5 (2009)


Article DOI: 10.1016/j.bmcl.2009.09.123
BindingDB Entry DOI: 10.7270/Q2Q52PRR
More data for this
Ligand-Target Pair
Insulin receptor


(Homo sapiens (Human))
BDBM50311895
PNG
(CHEMBL1076480 | N-(3-(1-(6-(2-methoxyethylamino)py...)
Show SMILES COCCNc1cc(ncn1)-n1c(Nc2cc(NC(=O)c3cccc(c3)C(F)(F)F)ccc2C)nc2ccccc12
Show InChI InChI=1S/C29H26F3N7O2/c1-18-10-11-21(36-27(40)19-6-5-7-20(14-19)29(30,31)32)15-23(18)38-28-37-22-8-3-4-9-24(22)39(28)26-16-25(34-17-35-26)33-12-13-41-2/h3-11,14-17H,12-13H2,1-2H3,(H,36,40)(H,37,38)(H,33,34,35)
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n/an/a>1.00E+4n/an/an/an/an/an/a



Genomics Institute of the Novartis Research Foundation (GNF)

Curated by ChEMBL


Assay Description
Inhibition of Tel-fused InsR expressed in mouse BAF3 cells


Bioorg Med Chem Lett 19: 6691-5 (2009)


Article DOI: 10.1016/j.bmcl.2009.09.123
BindingDB Entry DOI: 10.7270/Q2Q52PRR
More data for this
Ligand-Target Pair
Insulin receptor


(Homo sapiens (Human))
BDBM50311893
PNG
(CHEMBL1076478 | N-(4-methyl-3-(1-(6-(3-(4-methylpi...)
Show SMILES CN1CCN(CCCNc2cc(ncn2)-n2c(Nc3cc(NC(=O)c4cccc(c4)C(F)(F)F)ccc3C)nc3ccccc23)CC1
Show InChI InChI=1S/C34H36F3N9O/c1-23-11-12-26(41-32(47)24-7-5-8-25(19-24)34(35,36)37)20-28(23)43-33-42-27-9-3-4-10-29(27)46(33)31-21-30(39-22-40-31)38-13-6-14-45-17-15-44(2)16-18-45/h3-5,7-12,19-22H,6,13-18H2,1-2H3,(H,41,47)(H,42,43)(H,38,39,40)
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n/an/a 3.16E+3n/an/an/an/an/an/a



Genomics Institute of the Novartis Research Foundation (GNF)

Curated by ChEMBL


Assay Description
Inhibition of Tel-fused InsR expressed in mouse BAF3 cells


Bioorg Med Chem Lett 19: 6691-5 (2009)


Article DOI: 10.1016/j.bmcl.2009.09.123
BindingDB Entry DOI: 10.7270/Q2Q52PRR
More data for this
Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))
BDBM50311917
PNG
(CHEMBL1079945 | N-(3-(1-(6-aminopyrimidin-4-yl)-1H...)
Show SMILES Cc1ccc(NC(=O)c2cccc(c2)C(F)(F)F)cc1Nc1nc2ccccc2n1-c1cc(N)ncn1
Show InChI InChI=1S/C26H20F3N7O/c1-15-9-10-18(33-24(37)16-5-4-6-17(11-16)26(27,28)29)12-20(15)35-25-34-19-7-2-3-8-21(19)36(25)23-13-22(30)31-14-32-23/h2-14H,1H3,(H,33,37)(H,34,35)(H2,30,31,32)
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n/an/a 78n/an/an/an/an/an/a



Genomics Institute of the Novartis Research Foundation (GNF)

Curated by ChEMBL


Assay Description
Inhibition of Tel-fused SRC expressed in mouse BAF3 cells


Bioorg Med Chem Lett 19: 6691-5 (2009)


Article DOI: 10.1016/j.bmcl.2009.09.123
BindingDB Entry DOI: 10.7270/Q2Q52PRR
More data for this
Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))
BDBM50311916
PNG
(CHEMBL1079422 | N-(3-(1-(6-aminopyrimidin-4-yl)-1H...)
Show SMILES Cc1ccc(NC(=O)c2cccc(Cl)c2)cc1Nc1nc2ccccc2n1-c1cc(N)ncn1
Show InChI InChI=1S/C25H20ClN7O/c1-15-9-10-18(30-24(34)16-5-4-6-17(26)11-16)12-20(15)32-25-31-19-7-2-3-8-21(19)33(25)23-13-22(27)28-14-29-23/h2-14H,1H3,(H,30,34)(H,31,32)(H2,27,28,29)
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n/an/a 1.65E+3n/an/an/an/an/an/a



Genomics Institute of the Novartis Research Foundation (GNF)

Curated by ChEMBL


Assay Description
Inhibition of SRC


Bioorg Med Chem Lett 19: 6691-5 (2009)


Article DOI: 10.1016/j.bmcl.2009.09.123
BindingDB Entry DOI: 10.7270/Q2Q52PRR
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50311890
PNG
(3-(1-(6-(4-(dimethylamino)butylamino)pyrimidin-4-y...)
Show SMILES CN(C)CCCCNc1cc(ncn1)-n1c(Nc2cc(ccc2C)C(=O)Nc2cccc(C)c2)nc2ccccc12
Show InChI InChI=1S/C32H36N8O/c1-22-10-9-11-25(18-22)36-31(41)24-15-14-23(2)27(19-24)38-32-37-26-12-5-6-13-28(26)40(32)30-20-29(34-21-35-30)33-16-7-8-17-39(3)4/h5-6,9-15,18-21H,7-8,16-17H2,1-4H3,(H,36,41)(H,37,38)(H,33,34,35)
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n/an/a 531n/an/an/an/an/an/a



Genomics Institute of the Novartis Research Foundation (GNF)

Curated by ChEMBL


Assay Description
Inhibition of Tel-fused LCK expressed in mouse BAF3 cells


Bioorg Med Chem Lett 19: 6691-5 (2009)


Article DOI: 10.1016/j.bmcl.2009.09.123
BindingDB Entry DOI: 10.7270/Q2Q52PRR
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50311889
PNG
(3-(1-(6-aminopyrimidin-4-yl)-1H-benzo[d]imidazol-2...)
Show SMILES Cc1cn(cn1)-c1cc(NC(=O)c2ccc(C)c(Nc3nc4ccccc4n3-c3cc(N)ncn3)c2)cc(c1)C(F)(F)F
Show InChI InChI=1S/C30H24F3N9O/c1-17-7-8-19(28(43)38-21-10-20(30(31,32)33)11-22(12-21)41-14-18(2)37-16-41)9-24(17)40-29-39-23-5-3-4-6-25(23)42(29)27-13-26(34)35-15-36-27/h3-16H,1-2H3,(H,38,43)(H,39,40)(H2,34,35,36)
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n/an/a 14n/an/an/an/an/an/a



Genomics Institute of the Novartis Research Foundation (GNF)

Curated by ChEMBL


Assay Description
Inhibition of Tel-fused LCK expressed in mouse BAF3 cells


Bioorg Med Chem Lett 19: 6691-5 (2009)


Article DOI: 10.1016/j.bmcl.2009.09.123
BindingDB Entry DOI: 10.7270/Q2Q52PRR
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50311909
PNG
(3-(1-(6-(4-(dimethylamino)butylamino)pyrimidin-4-y...)
Show SMILES CN(C)CCCCNc1cc(ncn1)-n1c(Nc2cc(ccc2C)C(=O)Nc2cccc(c2)C(F)(F)F)nc2ccccc12
Show InChI InChI=1S/C32H33F3N8O/c1-21-13-14-22(30(44)39-24-10-8-9-23(18-24)32(33,34)35)17-26(21)41-31-40-25-11-4-5-12-27(25)43(31)29-19-28(37-20-38-29)36-15-6-7-16-42(2)3/h4-5,8-14,17-20H,6-7,15-16H2,1-3H3,(H,39,44)(H,40,41)(H,36,37,38)
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n/an/a 38n/an/an/an/an/an/a



Genomics Institute of the Novartis Research Foundation (GNF)

Curated by ChEMBL


Assay Description
Inhibition of Tel-fused LCK expressed in mouse BAF3 cells


Bioorg Med Chem Lett 19: 6691-5 (2009)


Article DOI: 10.1016/j.bmcl.2009.09.123
BindingDB Entry DOI: 10.7270/Q2Q52PRR
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50311908
PNG
(4-methyl-3-(1-(6-(3-(4-methylpiperazin-1-yl)propyl...)
Show SMILES CN1CCN(CCCNc2cc(ncn2)-n2c(Nc3cc(ccc3C)C(=O)Nc3cccc(C)c3)nc3ccccc23)CC1
Show InChI InChI=1S/C34H39N9O/c1-24-8-6-9-27(20-24)38-33(44)26-13-12-25(2)29(21-26)40-34-39-28-10-4-5-11-30(28)43(34)32-22-31(36-23-37-32)35-14-7-15-42-18-16-41(3)17-19-42/h4-6,8-13,20-23H,7,14-19H2,1-3H3,(H,38,44)(H,39,40)(H,35,36,37)
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n/an/a 337n/an/an/an/an/an/a



Genomics Institute of the Novartis Research Foundation (GNF)

Curated by ChEMBL


Assay Description
Inhibition of Tel-fused LCK expressed in mouse BAF3 cells


Bioorg Med Chem Lett 19: 6691-5 (2009)


Article DOI: 10.1016/j.bmcl.2009.09.123
BindingDB Entry DOI: 10.7270/Q2Q52PRR
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50311891
PNG
(3-(1-(6-(4-(diethylamino)butylamino)pyrimidin-4-yl...)
Show SMILES CCN(CC)CCCCNc1cc(ncn1)-n1c(Nc2cc(ccc2C)C(=O)Nc2cccc(C)c2)nc2ccccc12
Show InChI InChI=1S/C34H40N8O/c1-5-41(6-2)19-10-9-18-35-31-22-32(37-23-36-31)42-30-15-8-7-14-28(30)39-34(42)40-29-21-26(17-16-25(29)4)33(43)38-27-13-11-12-24(3)20-27/h7-8,11-17,20-23H,5-6,9-10,18-19H2,1-4H3,(H,38,43)(H,39,40)(H,35,36,37)
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n/an/a 406n/an/an/an/an/an/a



Genomics Institute of the Novartis Research Foundation (GNF)

Curated by ChEMBL


Assay Description
Inhibition of Tel-fused LCK expressed in mouse BAF3 cells


Bioorg Med Chem Lett 19: 6691-5 (2009)


Article DOI: 10.1016/j.bmcl.2009.09.123
BindingDB Entry DOI: 10.7270/Q2Q52PRR
More data for this
Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))
BDBM50311910
PNG
(3-(1-(6-(4-(diethylamino)butylamino)pyrimidin-4-yl...)
Show SMILES CCN(CC)CCCCNc1cc(ncn1)-n1c(Nc2cc(ccc2C)C(=O)Nc2cccc(c2)C(F)(F)F)nc2ccccc12
Show InChI InChI=1S/C34H37F3N8O/c1-4-44(5-2)18-9-8-17-38-30-21-31(40-22-39-30)45-29-14-7-6-13-27(29)42-33(45)43-28-19-24(16-15-23(28)3)32(46)41-26-12-10-11-25(20-26)34(35,36)37/h6-7,10-16,19-22H,4-5,8-9,17-18H2,1-3H3,(H,41,46)(H,42,43)(H,38,39,40)
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n/an/a 274n/an/an/an/an/an/a



Genomics Institute of the Novartis Research Foundation (GNF)

Curated by ChEMBL


Assay Description
Inhibition of SRC


Bioorg Med Chem Lett 19: 6691-5 (2009)


Article DOI: 10.1016/j.bmcl.2009.09.123
BindingDB Entry DOI: 10.7270/Q2Q52PRR
More data for this
Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))
BDBM50311911
PNG
(4-methyl-3-(1-(6-(2-(4-methylpiperazin-1-yl)ethyla...)
Show SMILES CN1CCN(CCNc2cc(ncn2)-n2c(Nc3cc(ccc3C)C(=O)Nc3cccc(c3)C(F)(F)F)nc3ccccc23)CC1
Show InChI InChI=1S/C33H34F3N9O/c1-22-10-11-23(31(46)40-25-7-5-6-24(19-25)33(34,35)36)18-27(22)42-32-41-26-8-3-4-9-28(26)45(32)30-20-29(38-21-39-30)37-12-13-44-16-14-43(2)15-17-44/h3-11,18-21H,12-17H2,1-2H3,(H,40,46)(H,41,42)(H,37,38,39)
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n/an/a 458n/an/an/an/an/an/a



Genomics Institute of the Novartis Research Foundation (GNF)

Curated by ChEMBL


Assay Description
Inhibition of SRC


Bioorg Med Chem Lett 19: 6691-5 (2009)


Article DOI: 10.1016/j.bmcl.2009.09.123
BindingDB Entry DOI: 10.7270/Q2Q52PRR
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50311910
PNG
(3-(1-(6-(4-(diethylamino)butylamino)pyrimidin-4-yl...)
Show SMILES CCN(CC)CCCCNc1cc(ncn1)-n1c(Nc2cc(ccc2C)C(=O)Nc2cccc(c2)C(F)(F)F)nc2ccccc12
Show InChI InChI=1S/C34H37F3N8O/c1-4-44(5-2)18-9-8-17-38-30-21-31(40-22-39-30)45-29-14-7-6-13-27(29)42-33(45)43-28-19-24(16-15-23(28)3)32(46)41-26-12-10-11-25(20-26)34(35,36)37/h6-7,10-16,19-22H,4-5,8-9,17-18H2,1-3H3,(H,41,46)(H,42,43)(H,38,39,40)
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n/an/a 18n/an/an/an/an/an/a



Genomics Institute of the Novartis Research Foundation (GNF)

Curated by ChEMBL


Assay Description
Inhibition of LCK


Bioorg Med Chem Lett 19: 6691-5 (2009)


Article DOI: 10.1016/j.bmcl.2009.09.123
BindingDB Entry DOI: 10.7270/Q2Q52PRR
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50311911
PNG
(4-methyl-3-(1-(6-(2-(4-methylpiperazin-1-yl)ethyla...)
Show SMILES CN1CCN(CCNc2cc(ncn2)-n2c(Nc3cc(ccc3C)C(=O)Nc3cccc(c3)C(F)(F)F)nc3ccccc23)CC1
Show InChI InChI=1S/C33H34F3N9O/c1-22-10-11-23(31(46)40-25-7-5-6-24(19-25)33(34,35)36)18-27(22)42-32-41-26-8-3-4-9-28(26)45(32)30-20-29(38-21-39-30)37-12-13-44-16-14-43(2)15-17-44/h3-11,18-21H,12-17H2,1-2H3,(H,40,46)(H,41,42)(H,37,38,39)
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n/an/a 11n/an/an/an/an/an/a



Genomics Institute of the Novartis Research Foundation (GNF)

Curated by ChEMBL


Assay Description
Inhibition of LCK


Bioorg Med Chem Lett 19: 6691-5 (2009)


Article DOI: 10.1016/j.bmcl.2009.09.123
BindingDB Entry DOI: 10.7270/Q2Q52PRR
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50311912
PNG
(4-methyl-3-(1-(6-(3-(4-methylpiperazin-1-yl)propyl...)
Show SMILES CN1CCN(CCCNc2cc(ncn2)-n2c(Nc3cc(ccc3C)C(=O)Nc3cccc(c3)C(F)(F)F)nc3ccccc23)CC1
Show InChI InChI=1S/C34H36F3N9O/c1-23-11-12-24(32(47)41-26-8-5-7-25(20-26)34(35,36)37)19-28(23)43-33-42-27-9-3-4-10-29(27)46(33)31-21-30(39-22-40-31)38-13-6-14-45-17-15-44(2)16-18-45/h3-5,7-12,19-22H,6,13-18H2,1-2H3,(H,41,47)(H,42,43)(H,38,39,40)
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n/an/a 18n/an/an/an/an/an/a



Genomics Institute of the Novartis Research Foundation (GNF)

Curated by ChEMBL


Assay Description
Inhibition of LCK


Bioorg Med Chem Lett 19: 6691-5 (2009)


Article DOI: 10.1016/j.bmcl.2009.09.123
BindingDB Entry DOI: 10.7270/Q2Q52PRR
More data for this
Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))
BDBM50311912
PNG
(4-methyl-3-(1-(6-(3-(4-methylpiperazin-1-yl)propyl...)
Show SMILES CN1CCN(CCCNc2cc(ncn2)-n2c(Nc3cc(ccc3C)C(=O)Nc3cccc(c3)C(F)(F)F)nc3ccccc23)CC1
Show InChI InChI=1S/C34H36F3N9O/c1-23-11-12-24(32(47)41-26-8-5-7-25(20-26)34(35,36)37)19-28(23)43-33-42-27-9-3-4-10-29(27)46(33)31-21-30(39-22-40-31)38-13-6-14-45-17-15-44(2)16-18-45/h3-5,7-12,19-22H,6,13-18H2,1-2H3,(H,41,47)(H,42,43)(H,38,39,40)
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n/an/a 494n/an/an/an/an/an/a



Genomics Institute of the Novartis Research Foundation (GNF)

Curated by ChEMBL


Assay Description
Inhibition of SRC


Bioorg Med Chem Lett 19: 6691-5 (2009)


Article DOI: 10.1016/j.bmcl.2009.09.123
BindingDB Entry DOI: 10.7270/Q2Q52PRR
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50311913
PNG
(3-(1-(6-(2-cyanoethylamino)pyrimidin-4-yl)-1H-benz...)
Show SMILES Cc1ccc(cc1Nc1nc2ccccc2n1-c1cc(NCCC#N)ncn1)C(=O)Nc1cccc(c1)C(F)(F)F
Show InChI InChI=1S/C29H23F3N8O/c1-18-10-11-19(27(41)37-21-7-4-6-20(15-21)29(30,31)32)14-23(18)39-28-38-22-8-2-3-9-24(22)40(28)26-16-25(35-17-36-26)34-13-5-12-33/h2-4,6-11,14-17H,5,13H2,1H3,(H,37,41)(H,38,39)(H,34,35,36)
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n/an/a 1.37E+3n/an/an/an/an/an/a



Genomics Institute of the Novartis Research Foundation (GNF)

Curated by ChEMBL


Assay Description
Inhibition of LCK


Bioorg Med Chem Lett 19: 6691-5 (2009)


Article DOI: 10.1016/j.bmcl.2009.09.123
BindingDB Entry DOI: 10.7270/Q2Q52PRR
More data for this
Ligand-Target Pair
Insulin receptor


(Homo sapiens (Human))
BDBM50311910
PNG
(3-(1-(6-(4-(diethylamino)butylamino)pyrimidin-4-yl...)
Show SMILES CCN(CC)CCCCNc1cc(ncn1)-n1c(Nc2cc(ccc2C)C(=O)Nc2cccc(c2)C(F)(F)F)nc2ccccc12
Show InChI InChI=1S/C34H37F3N8O/c1-4-44(5-2)18-9-8-17-38-30-21-31(40-22-39-30)45-29-14-7-6-13-27(29)42-33(45)43-28-19-24(16-15-23(28)3)32(46)41-26-12-10-11-25(20-26)34(35,36)37/h6-7,10-16,19-22H,4-5,8-9,17-18H2,1-3H3,(H,41,46)(H,42,43)(H,38,39,40)
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n/an/a 1.81E+3n/an/an/an/an/an/a



Genomics Institute of the Novartis Research Foundation (GNF)

Curated by ChEMBL


Assay Description
Inhibition of Tel-fused InsR expressed in mouse BAF3 cells


Bioorg Med Chem Lett 19: 6691-5 (2009)


Article DOI: 10.1016/j.bmcl.2009.09.123
BindingDB Entry DOI: 10.7270/Q2Q52PRR
More data for this
Ligand-Target Pair
Insulin receptor


(Homo sapiens (Human))
BDBM50311913
PNG
(3-(1-(6-(2-cyanoethylamino)pyrimidin-4-yl)-1H-benz...)
Show SMILES Cc1ccc(cc1Nc1nc2ccccc2n1-c1cc(NCCC#N)ncn1)C(=O)Nc1cccc(c1)C(F)(F)F
Show InChI InChI=1S/C29H23F3N8O/c1-18-10-11-19(27(41)37-21-7-4-6-20(15-21)29(30,31)32)14-23(18)39-28-38-22-8-2-3-9-24(22)40(28)26-16-25(35-17-36-26)34-13-5-12-33/h2-4,6-11,14-17H,5,13H2,1H3,(H,37,41)(H,38,39)(H,34,35,36)
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n/an/a 1.09E+3n/an/an/an/an/an/a



Genomics Institute of the Novartis Research Foundation (GNF)

Curated by ChEMBL


Assay Description
Inhibition of Tel-fused InsR expressed in mouse BAF3 cells


Bioorg Med Chem Lett 19: 6691-5 (2009)


Article DOI: 10.1016/j.bmcl.2009.09.123
BindingDB Entry DOI: 10.7270/Q2Q52PRR
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50311901
PNG
(3-(1-(6-aminopyrimidin-4-yl)-1H-benzo[d]imidazol-2...)
Show SMILES Cc1ccc(cc1Nc1nc2ccccc2n1-c1cc(N)ncn1)C(=O)Nc1cccc(c1)C(F)(F)F
Show InChI InChI=1S/C26H20F3N7O/c1-15-9-10-16(24(37)33-18-6-4-5-17(12-18)26(27,28)29)11-20(15)35-25-34-19-7-2-3-8-21(19)36(25)23-13-22(30)31-14-32-23/h2-14H,1H3,(H,33,37)(H,34,35)(H2,30,31,32)
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n/an/a 20n/an/an/an/an/an/a



Genomics Institute of the Novartis Research Foundation (GNF)

Curated by ChEMBL


Assay Description
Inhibition of Tel-fused LCK expressed in mouse BAF3 cells


Bioorg Med Chem Lett 19: 6691-5 (2009)


Article DOI: 10.1016/j.bmcl.2009.09.123
BindingDB Entry DOI: 10.7270/Q2Q52PRR
More data for this
Ligand-Target Pair
Insulin receptor


(Homo sapiens (Human))
BDBM50311912
PNG
(4-methyl-3-(1-(6-(3-(4-methylpiperazin-1-yl)propyl...)
Show SMILES CN1CCN(CCCNc2cc(ncn2)-n2c(Nc3cc(ccc3C)C(=O)Nc3cccc(c3)C(F)(F)F)nc3ccccc23)CC1
Show InChI InChI=1S/C34H36F3N9O/c1-23-11-12-24(32(47)41-26-8-5-7-25(20-26)34(35,36)37)19-28(23)43-33-42-27-9-3-4-10-29(27)46(33)31-21-30(39-22-40-31)38-13-6-14-45-17-15-44(2)16-18-45/h3-5,7-12,19-22H,6,13-18H2,1-2H3,(H,41,47)(H,42,43)(H,38,39,40)
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n/an/a 1.86E+3n/an/an/an/an/an/a



Genomics Institute of the Novartis Research Foundation (GNF)

Curated by ChEMBL


Assay Description
Inhibition of Tel-fused InsR expressed in mouse BAF3 cells


Bioorg Med Chem Lett 19: 6691-5 (2009)


Article DOI: 10.1016/j.bmcl.2009.09.123
BindingDB Entry DOI: 10.7270/Q2Q52PRR
More data for this
Ligand-Target Pair
Insulin receptor


(Homo sapiens (Human))
BDBM50311889
PNG
(3-(1-(6-aminopyrimidin-4-yl)-1H-benzo[d]imidazol-2...)
Show SMILES Cc1cn(cn1)-c1cc(NC(=O)c2ccc(C)c(Nc3nc4ccccc4n3-c3cc(N)ncn3)c2)cc(c1)C(F)(F)F
Show InChI InChI=1S/C30H24F3N9O/c1-17-7-8-19(28(43)38-21-10-20(30(31,32)33)11-22(12-21)41-14-18(2)37-16-41)9-24(17)40-29-39-23-5-3-4-6-25(23)42(29)27-13-26(34)35-15-36-27/h3-16H,1-2H3,(H,38,43)(H,39,40)(H2,34,35,36)
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n/an/a 7.63E+3n/an/an/an/an/an/a



Genomics Institute of the Novartis Research Foundation (GNF)

Curated by ChEMBL


Assay Description
Inhibition of Tel-fused InsR expressed in mouse BAF3 cells


Bioorg Med Chem Lett 19: 6691-5 (2009)


Article DOI: 10.1016/j.bmcl.2009.09.123
BindingDB Entry DOI: 10.7270/Q2Q52PRR
More data for this
Ligand-Target Pair
Insulin receptor


(Homo sapiens (Human))
BDBM50311891
PNG
(3-(1-(6-(4-(diethylamino)butylamino)pyrimidin-4-yl...)
Show SMILES CCN(CC)CCCCNc1cc(ncn1)-n1c(Nc2cc(ccc2C)C(=O)Nc2cccc(C)c2)nc2ccccc12
Show InChI InChI=1S/C34H40N8O/c1-5-41(6-2)19-10-9-18-35-31-22-32(37-23-36-31)42-30-15-8-7-14-28(30)39-34(42)40-29-21-26(17-16-25(29)4)33(43)38-27-13-11-12-24(3)20-27/h7-8,11-17,20-23H,5-6,9-10,18-19H2,1-4H3,(H,38,43)(H,39,40)(H,35,36,37)
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n/an/a 2.26E+3n/an/an/an/an/an/a



Genomics Institute of the Novartis Research Foundation (GNF)

Curated by ChEMBL


Assay Description
Inhibition of Tel-fused InsR expressed in mouse BAF3 cells


Bioorg Med Chem Lett 19: 6691-5 (2009)


Article DOI: 10.1016/j.bmcl.2009.09.123
BindingDB Entry DOI: 10.7270/Q2Q52PRR
More data for this
Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))
BDBM50311909
PNG
(3-(1-(6-(4-(dimethylamino)butylamino)pyrimidin-4-y...)
Show SMILES CN(C)CCCCNc1cc(ncn1)-n1c(Nc2cc(ccc2C)C(=O)Nc2cccc(c2)C(F)(F)F)nc2ccccc12
Show InChI InChI=1S/C32H33F3N8O/c1-21-13-14-22(30(44)39-24-10-8-9-23(18-24)32(33,34)35)17-26(21)41-31-40-25-11-4-5-12-27(25)43(31)29-19-28(37-20-38-29)36-15-6-7-16-42(2)3/h4-5,8-14,17-20H,6-7,15-16H2,1-3H3,(H,39,44)(H,40,41)(H,36,37,38)
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n/an/a 485n/an/an/an/an/an/a



Genomics Institute of the Novartis Research Foundation (GNF)

Curated by ChEMBL


Assay Description
Inhibition of SRC


Bioorg Med Chem Lett 19: 6691-5 (2009)


Article DOI: 10.1016/j.bmcl.2009.09.123
BindingDB Entry DOI: 10.7270/Q2Q52PRR
More data for this
Ligand-Target Pair
Insulin receptor


(Homo sapiens (Human))
BDBM50311890
PNG
(3-(1-(6-(4-(dimethylamino)butylamino)pyrimidin-4-y...)
Show SMILES CN(C)CCCCNc1cc(ncn1)-n1c(Nc2cc(ccc2C)C(=O)Nc2cccc(C)c2)nc2ccccc12
Show InChI InChI=1S/C32H36N8O/c1-22-10-9-11-25(18-22)36-31(41)24-15-14-23(2)27(19-24)38-32-37-26-12-5-6-13-28(26)40(32)30-20-29(34-21-35-30)33-16-7-8-17-39(3)4/h5-6,9-15,18-21H,7-8,16-17H2,1-4H3,(H,36,41)(H,37,38)(H,33,34,35)
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n/an/a 2.63E+3n/an/an/an/an/an/a



Genomics Institute of the Novartis Research Foundation (GNF)

Curated by ChEMBL


Assay Description
Inhibition of Tel-fused InsR expressed in mouse BAF3 cells


Bioorg Med Chem Lett 19: 6691-5 (2009)


Article DOI: 10.1016/j.bmcl.2009.09.123
BindingDB Entry DOI: 10.7270/Q2Q52PRR
More data for this
Ligand-Target Pair
Insulin receptor


(Homo sapiens (Human))
BDBM50311908
PNG
(4-methyl-3-(1-(6-(3-(4-methylpiperazin-1-yl)propyl...)
Show SMILES CN1CCN(CCCNc2cc(ncn2)-n2c(Nc3cc(ccc3C)C(=O)Nc3cccc(C)c3)nc3ccccc23)CC1
Show InChI InChI=1S/C34H39N9O/c1-24-8-6-9-27(20-24)38-33(44)26-13-12-25(2)29(21-26)40-34-39-28-10-4-5-11-30(28)43(34)32-22-31(36-23-37-32)35-14-7-15-42-18-16-41(3)17-19-42/h4-6,8-13,20-23H,7,14-19H2,1-3H3,(H,38,44)(H,39,40)(H,35,36,37)
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n/an/a 3.19E+3n/an/an/an/an/an/a



Genomics Institute of the Novartis Research Foundation (GNF)

Curated by ChEMBL


Assay Description
Inhibition of Tel-fused InsR expressed in mouse BAF3 cells


Bioorg Med Chem Lett 19: 6691-5 (2009)


Article DOI: 10.1016/j.bmcl.2009.09.123
BindingDB Entry DOI: 10.7270/Q2Q52PRR
More data for this
Ligand-Target Pair
Insulin receptor


(Homo sapiens (Human))
BDBM50311909
PNG
(3-(1-(6-(4-(dimethylamino)butylamino)pyrimidin-4-y...)
Show SMILES CN(C)CCCCNc1cc(ncn1)-n1c(Nc2cc(ccc2C)C(=O)Nc2cccc(c2)C(F)(F)F)nc2ccccc12
Show InChI InChI=1S/C32H33F3N8O/c1-21-13-14-22(30(44)39-24-10-8-9-23(18-24)32(33,34)35)17-26(21)41-31-40-25-11-4-5-12-27(25)43(31)29-19-28(37-20-38-29)36-15-6-7-16-42(2)3/h4-5,8-14,17-20H,6-7,15-16H2,1-3H3,(H,39,44)(H,40,41)(H,36,37,38)
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n/an/a 1.22E+3n/an/an/an/an/an/a



Genomics Institute of the Novartis Research Foundation (GNF)

Curated by ChEMBL


Assay Description
Inhibition of Tel-fused InsR expressed in mouse BAF3 cells


Bioorg Med Chem Lett 19: 6691-5 (2009)


Article DOI: 10.1016/j.bmcl.2009.09.123
BindingDB Entry DOI: 10.7270/Q2Q52PRR
More data for this
Ligand-Target Pair
Insulin receptor


(Homo sapiens (Human))
BDBM50311901
PNG
(3-(1-(6-aminopyrimidin-4-yl)-1H-benzo[d]imidazol-2...)
Show SMILES Cc1ccc(cc1Nc1nc2ccccc2n1-c1cc(N)ncn1)C(=O)Nc1cccc(c1)C(F)(F)F
Show InChI InChI=1S/C26H20F3N7O/c1-15-9-10-16(24(37)33-18-6-4-5-17(12-18)26(27,28)29)11-20(15)35-25-34-19-7-2-3-8-21(19)36(25)23-13-22(30)31-14-32-23/h2-14H,1H3,(H,33,37)(H,34,35)(H2,30,31,32)
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n/an/a>1.00E+4n/an/an/an/an/an/a



Genomics Institute of the Novartis Research Foundation (GNF)

Curated by ChEMBL


Assay Description
Inhibition of Tel-fused InsR expressed in mouse BAF3 cells


Bioorg Med Chem Lett 19: 6691-5 (2009)


Article DOI: 10.1016/j.bmcl.2009.09.123
BindingDB Entry DOI: 10.7270/Q2Q52PRR
More data for this
Ligand-Target Pair
Insulin receptor


(Homo sapiens (Human))
BDBM50311916
PNG
(CHEMBL1079422 | N-(3-(1-(6-aminopyrimidin-4-yl)-1H...)
Show SMILES Cc1ccc(NC(=O)c2cccc(Cl)c2)cc1Nc1nc2ccccc2n1-c1cc(N)ncn1
Show InChI InChI=1S/C25H20ClN7O/c1-15-9-10-18(30-24(34)16-5-4-6-17(26)11-16)12-20(15)32-25-31-19-7-2-3-8-21(19)33(25)23-13-22(27)28-14-29-23/h2-14H,1H3,(H,30,34)(H,31,32)(H2,27,28,29)
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n/an/a 1.99E+3n/an/an/an/an/an/a



Genomics Institute of the Novartis Research Foundation (GNF)

Curated by ChEMBL


Assay Description
Inhibition of Tel-fused InsR expressed in mouse BAF3 cells


Bioorg Med Chem Lett 19: 6691-5 (2009)


Article DOI: 10.1016/j.bmcl.2009.09.123
BindingDB Entry DOI: 10.7270/Q2Q52PRR
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lck


(Homo sapiens (Human))
BDBM50311916
PNG
(CHEMBL1079422 | N-(3-(1-(6-aminopyrimidin-4-yl)-1H...)
Show SMILES Cc1ccc(NC(=O)c2cccc(Cl)c2)cc1Nc1nc2ccccc2n1-c1cc(N)ncn1
Show InChI InChI=1S/C25H20ClN7O/c1-15-9-10-18(30-24(34)16-5-4-6-17(26)11-16)12-20(15)32-25-31-19-7-2-3-8-21(19)33(25)23-13-22(27)28-14-29-23/h2-14H,1H3,(H,30,34)(H,31,32)(H2,27,28,29)
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n/an/a 132n/an/an/an/an/an/a



Genomics Institute of the Novartis Research Foundation (GNF)

Curated by ChEMBL


Assay Description
Inhibition of LCK


Bioorg Med Chem Lett 19: 6691-5 (2009)


Article DOI: 10.1016/j.bmcl.2009.09.123
BindingDB Entry DOI: 10.7270/Q2Q52PRR
More data for this
Ligand-Target Pair
Insulin receptor


(Homo sapiens (Human))
BDBM50311911
PNG
(4-methyl-3-(1-(6-(2-(4-methylpiperazin-1-yl)ethyla...)
Show SMILES CN1CCN(CCNc2cc(ncn2)-n2c(Nc3cc(ccc3C)C(=O)Nc3cccc(c3)C(F)(F)F)nc3ccccc23)CC1
Show InChI InChI=1S/C33H34F3N9O/c1-22-10-11-23(31(46)40-25-7-5-6-24(19-25)33(34,35)36)18-27(22)42-32-41-26-8-3-4-9-28(26)45(32)30-20-29(38-21-39-30)37-12-13-44-16-14-43(2)15-17-44/h3-11,18-21H,12-17H2,1-2H3,(H,40,46)(H,41,42)(H,37,38,39)
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n/an/a 1.51E+3n/an/an/an/an/an/a



Genomics Institute of the Novartis Research Foundation (GNF)

Curated by ChEMBL


Assay Description
Inhibition of Tel-fused InsR expressed in mouse BAF3 cells


Bioorg Med Chem Lett 19: 6691-5 (2009)


Article DOI: 10.1016/j.bmcl.2009.09.123
BindingDB Entry DOI: 10.7270/Q2Q52PRR
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lyn


(Homo sapiens (Human))
BDBM50311889
PNG
(3-(1-(6-aminopyrimidin-4-yl)-1H-benzo[d]imidazol-2...)
Show SMILES Cc1cn(cn1)-c1cc(NC(=O)c2ccc(C)c(Nc3nc4ccccc4n3-c3cc(N)ncn3)c2)cc(c1)C(F)(F)F
Show InChI InChI=1S/C30H24F3N9O/c1-17-7-8-19(28(43)38-21-10-20(30(31,32)33)11-22(12-21)41-14-18(2)37-16-41)9-24(17)40-29-39-23-5-3-4-6-25(23)42(29)27-13-26(34)35-15-36-27/h3-16H,1-2H3,(H,38,43)(H,39,40)(H2,34,35,36)
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n/an/a 28n/an/an/an/an/an/a



Genomics Institute of the Novartis Research Foundation (GNF)

Curated by ChEMBL


Assay Description
Inhibition of Tel-fused LYN expressed in mouse BAF3 cells


Bioorg Med Chem Lett 19: 6691-5 (2009)


Article DOI: 10.1016/j.bmcl.2009.09.123
BindingDB Entry DOI: 10.7270/Q2Q52PRR
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lyn


(Homo sapiens (Human))
BDBM50311890
PNG
(3-(1-(6-(4-(dimethylamino)butylamino)pyrimidin-4-y...)
Show SMILES CN(C)CCCCNc1cc(ncn1)-n1c(Nc2cc(ccc2C)C(=O)Nc2cccc(C)c2)nc2ccccc12
Show InChI InChI=1S/C32H36N8O/c1-22-10-9-11-25(18-22)36-31(41)24-15-14-23(2)27(19-24)38-32-37-26-12-5-6-13-28(26)40(32)30-20-29(34-21-35-30)33-16-7-8-17-39(3)4/h5-6,9-15,18-21H,7-8,16-17H2,1-4H3,(H,36,41)(H,37,38)(H,33,34,35)
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n/an/a 1.38E+3n/an/an/an/an/an/a



Genomics Institute of the Novartis Research Foundation (GNF)

Curated by ChEMBL


Assay Description
Inhibition of Tel-fused LYN expressed in mouse BAF3 cells


Bioorg Med Chem Lett 19: 6691-5 (2009)


Article DOI: 10.1016/j.bmcl.2009.09.123
BindingDB Entry DOI: 10.7270/Q2Q52PRR
More data for this
Ligand-Target Pair
Tyrosine-protein kinase Lyn


(Homo sapiens (Human))
BDBM50311891
PNG
(3-(1-(6-(4-(diethylamino)butylamino)pyrimidin-4-yl...)
Show SMILES CCN(CC)CCCCNc1cc(ncn1)-n1c(Nc2cc(ccc2C)C(=O)Nc2cccc(C)c2)nc2ccccc12
Show InChI InChI=1S/C34H40N8O/c1-5-41(6-2)19-10-9-18-35-31-22-32(37-23-36-31)42-30-15-8-7-14-28(30)39-34(42)40-29-21-26(17-16-25(29)4)33(43)38-27-13-11-12-24(3)20-27/h7-8,11-17,20-23H,5-6,9-10,18-19H2,1-4H3,(H,38,43)(H,39,40)(H,35,36,37)
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n/an/a 1.32E+3n/an/an/an/an/an/a



Genomics Institute of the Novartis Research Foundation (GNF)

Curated by ChEMBL


Assay Description
Inhibition of Tel-fused LYN expressed in mouse BAF3 cells


Bioorg Med Chem Lett 19: 6691-5 (2009)


Article DOI: 10.1016/j.bmcl.2009.09.123
BindingDB Entry DOI: 10.7270/Q2Q52PRR
More data for this
Ligand-Target Pair
Tyrosine-protein kinase HCK


(Homo sapiens (Human))
BDBM50311893
PNG
(CHEMBL1076478 | N-(4-methyl-3-(1-(6-(3-(4-methylpi...)
Show SMILES CN1CCN(CCCNc2cc(ncn2)-n2c(Nc3cc(NC(=O)c4cccc(c4)C(F)(F)F)ccc3C)nc3ccccc23)CC1
Show InChI InChI=1S/C34H36F3N9O/c1-23-11-12-26(41-32(47)24-7-5-8-25(19-24)34(35,36)37)20-28(23)43-33-42-27-9-3-4-10-29(27)46(33)31-21-30(39-22-40-31)38-13-6-14-45-17-15-44(2)16-18-45/h3-5,7-12,19-22H,6,13-18H2,1-2H3,(H,41,47)(H,42,43)(H,38,39,40)
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n/an/a 31n/an/an/an/an/an/a



Genomics Institute of the Novartis Research Foundation (GNF)

Curated by ChEMBL


Assay Description
Inhibition of HCK


Bioorg Med Chem Lett 19: 6691-5 (2009)


Article DOI: 10.1016/j.bmcl.2009.09.123
BindingDB Entry DOI: 10.7270/Q2Q52PRR
More data for this
Ligand-Target Pair
Tyrosine-protein kinase HCK


(Homo sapiens (Human))
BDBM50311894
PNG
(CHEMBL1087638 | N-(3-(1-(6-(2-hydroxyethylamino)py...)
Show SMILES Cc1ccc(NC(=O)c2cccc(c2)C(F)(F)F)cc1Nc1nc2ccccc2n1-c1cc(NCCO)ncn1
Show InChI InChI=1S/C28H24F3N7O2/c1-17-9-10-20(35-26(40)18-5-4-6-19(13-18)28(29,30)31)14-22(17)37-27-36-21-7-2-3-8-23(21)38(27)25-15-24(32-11-12-39)33-16-34-25/h2-10,13-16,39H,11-12H2,1H3,(H,35,40)(H,36,37)(H,32,33,34)
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n/an/a 192n/an/an/an/an/an/a



Genomics Institute of the Novartis Research Foundation (GNF)

Curated by ChEMBL


Assay Description
Inhibition of HCK


Bioorg Med Chem Lett 19: 6691-5 (2009)


Article DOI: 10.1016/j.bmcl.2009.09.123
BindingDB Entry DOI: 10.7270/Q2Q52PRR
More data for this
Ligand-Target Pair
Tyrosine-protein kinase HCK


(Homo sapiens (Human))
BDBM50311895
PNG
(CHEMBL1076480 | N-(3-(1-(6-(2-methoxyethylamino)py...)
Show SMILES COCCNc1cc(ncn1)-n1c(Nc2cc(NC(=O)c3cccc(c3)C(F)(F)F)ccc2C)nc2ccccc12
Show InChI InChI=1S/C29H26F3N7O2/c1-18-10-11-21(36-27(40)19-6-5-7-20(14-19)29(30,31)32)15-23(18)38-28-37-22-8-3-4-9-24(22)39(28)26-16-25(34-17-35-26)33-12-13-41-2/h3-11,14-17H,12-13H2,1-2H3,(H,36,40)(H,37,38)(H,33,34,35)
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n/an/a 405n/an/an/an/an/an/a



Genomics Institute of the Novartis Research Foundation (GNF)

Curated by ChEMBL


Assay Description
Inhibition of HCK


Bioorg Med Chem Lett 19: 6691-5 (2009)


Article DOI: 10.1016/j.bmcl.2009.09.123
BindingDB Entry DOI: 10.7270/Q2Q52PRR
More data for this
Ligand-Target Pair
Tyrosine-protein kinase HCK


(Homo sapiens (Human))
BDBM50311901
PNG
(3-(1-(6-aminopyrimidin-4-yl)-1H-benzo[d]imidazol-2...)
Show SMILES Cc1ccc(cc1Nc1nc2ccccc2n1-c1cc(N)ncn1)C(=O)Nc1cccc(c1)C(F)(F)F
Show InChI InChI=1S/C26H20F3N7O/c1-15-9-10-16(24(37)33-18-6-4-5-17(12-18)26(27,28)29)11-20(15)35-25-34-19-7-2-3-8-21(19)36(25)23-13-22(30)31-14-32-23/h2-14H,1H3,(H,33,37)(H,34,35)(H2,30,31,32)
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n/an/a>2.50E+3n/an/an/an/an/an/a



Genomics Institute of the Novartis Research Foundation (GNF)

Curated by ChEMBL


Assay Description
Inhibition of HCK


Bioorg Med Chem Lett 19: 6691-5 (2009)


Article DOI: 10.1016/j.bmcl.2009.09.123
BindingDB Entry DOI: 10.7270/Q2Q52PRR
More data for this
Ligand-Target Pair
Tyrosine-protein kinase HCK


(Homo sapiens (Human))
BDBM50311889
PNG
(3-(1-(6-aminopyrimidin-4-yl)-1H-benzo[d]imidazol-2...)
Show SMILES Cc1cn(cn1)-c1cc(NC(=O)c2ccc(C)c(Nc3nc4ccccc4n3-c3cc(N)ncn3)c2)cc(c1)C(F)(F)F
Show InChI InChI=1S/C30H24F3N9O/c1-17-7-8-19(28(43)38-21-10-20(30(31,32)33)11-22(12-21)41-14-18(2)37-16-41)9-24(17)40-29-39-23-5-3-4-6-25(23)42(29)27-13-26(34)35-15-36-27/h3-16H,1-2H3,(H,38,43)(H,39,40)(H2,34,35,36)
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n/an/a 904n/an/an/an/an/an/a



Genomics Institute of the Novartis Research Foundation (GNF)

Curated by ChEMBL


Assay Description
Inhibition of HCK


Bioorg Med Chem Lett 19: 6691-5 (2009)


Article DOI: 10.1016/j.bmcl.2009.09.123
BindingDB Entry DOI: 10.7270/Q2Q52PRR
More data for this
Ligand-Target Pair
Tyrosine-protein kinase HCK


(Homo sapiens (Human))
BDBM50311890
PNG
(3-(1-(6-(4-(dimethylamino)butylamino)pyrimidin-4-y...)
Show SMILES CN(C)CCCCNc1cc(ncn1)-n1c(Nc2cc(ccc2C)C(=O)Nc2cccc(C)c2)nc2ccccc12
Show InChI InChI=1S/C32H36N8O/c1-22-10-9-11-25(18-22)36-31(41)24-15-14-23(2)27(19-24)38-32-37-26-12-5-6-13-28(26)40(32)30-20-29(34-21-35-30)33-16-7-8-17-39(3)4/h5-6,9-15,18-21H,7-8,16-17H2,1-4H3,(H,36,41)(H,37,38)(H,33,34,35)
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n/an/a>2.50E+3n/an/an/an/an/an/a



Genomics Institute of the Novartis Research Foundation (GNF)

Curated by ChEMBL


Assay Description
Inhibition of HCK


Bioorg Med Chem Lett 19: 6691-5 (2009)


Article DOI: 10.1016/j.bmcl.2009.09.123
BindingDB Entry DOI: 10.7270/Q2Q52PRR
More data for this
Ligand-Target Pair
Tyrosine-protein kinase HCK


(Homo sapiens (Human))
BDBM50311891
PNG
(3-(1-(6-(4-(diethylamino)butylamino)pyrimidin-4-yl...)
Show SMILES CCN(CC)CCCCNc1cc(ncn1)-n1c(Nc2cc(ccc2C)C(=O)Nc2cccc(C)c2)nc2ccccc12
Show InChI InChI=1S/C34H40N8O/c1-5-41(6-2)19-10-9-18-35-31-22-32(37-23-36-31)42-30-15-8-7-14-28(30)39-34(42)40-29-21-26(17-16-25(29)4)33(43)38-27-13-11-12-24(3)20-27/h7-8,11-17,20-23H,5-6,9-10,18-19H2,1-4H3,(H,38,43)(H,39,40)(H,35,36,37)
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n/an/a 1.81E+3n/an/an/an/an/an/a



Genomics Institute of the Novartis Research Foundation (GNF)

Curated by ChEMBL


Assay Description
Inhibition of HCK


Bioorg Med Chem Lett 19: 6691-5 (2009)


Article DOI: 10.1016/j.bmcl.2009.09.123
BindingDB Entry DOI: 10.7270/Q2Q52PRR
More data for this
Ligand-Target Pair
Tyrosine-protein kinase HCK


(Homo sapiens (Human))
BDBM50311908
PNG
(4-methyl-3-(1-(6-(3-(4-methylpiperazin-1-yl)propyl...)
Show SMILES CN1CCN(CCCNc2cc(ncn2)-n2c(Nc3cc(ccc3C)C(=O)Nc3cccc(C)c3)nc3ccccc23)CC1
Show InChI InChI=1S/C34H39N9O/c1-24-8-6-9-27(20-24)38-33(44)26-13-12-25(2)29(21-26)40-34-39-28-10-4-5-11-30(28)43(34)32-22-31(36-23-37-32)35-14-7-15-42-18-16-41(3)17-19-42/h4-6,8-13,20-23H,7,14-19H2,1-3H3,(H,38,44)(H,39,40)(H,35,36,37)
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n/an/a 1.88E+3n/an/an/an/an/an/a



Genomics Institute of the Novartis Research Foundation (GNF)

Curated by ChEMBL


Assay Description
Inhibition of HCK


Bioorg Med Chem Lett 19: 6691-5 (2009)


Article DOI: 10.1016/j.bmcl.2009.09.123
BindingDB Entry DOI: 10.7270/Q2Q52PRR
More data for this
Ligand-Target Pair
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