Found 26 hits Enz. Inhib. hit(s) with all data for entry = 50017912 Target/Host (Institution) | Ligand | Target/Host Links | Ligand Links | Trg + Lig Links | Ki nM | ΔG° kJ/mole | IC50 nM | Kd nM | EC50/IC50 nM | koff s-1 | kon M-1s-1 | pH | Temp °C |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50188343
(4-(2,6-dichloro-phenyl)-8-[4-(2-diethylamino-ethox...)Show SMILES CCN(CC)CCOc1ccc(Nc2ncc3C=C(N4N(CCC4=O)c3n2)c2c(Cl)cccc2Cl)cc1 |c:17| Show InChI InChI=1S/C27H28Cl2N6O2/c1-3-33(4-2)14-15-37-20-10-8-19(9-11-20)31-27-30-17-18-16-23(25-21(28)6-5-7-22(25)29)35-24(36)12-13-34(35)26(18)32-27/h5-11,16-17H,3-4,12-15H2,1-2H3,(H,30,31,32) | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 2 | n/a | n/a | n/a | n/a | n/a | n/a |
Procter and Gamble Pharmaceuticals
Curated by ChEMBL
| Assay Description Inhibition of human recombinant Lck in presence of 10 mM ATP |
Bioorg Med Chem Lett 16: 4257-61 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.072 BindingDB Entry DOI: 10.7270/Q22V2FQD |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50188342
(4-(2,6-dichloro-phenyl)-8-(4-morpholin-4-yl-phenyl...)Show SMILES Clc1cccc(Cl)c1C1=Cc2cnc(Nc3ccc(cc3)N3CCOCC3)nc2N2CCC(=O)N12 |t:9| Show InChI InChI=1S/C25H22Cl2N6O2/c26-19-2-1-3-20(27)23(19)21-14-16-15-28-25(30-24(16)32-9-8-22(34)33(21)32)29-17-4-6-18(7-5-17)31-10-12-35-13-11-31/h1-7,14-15H,8-13H2,(H,28,29,30) | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 3 | n/a | n/a | n/a | n/a | n/a | n/a |
Procter and Gamble Pharmaceuticals
Curated by ChEMBL
| Assay Description Inhibition of human recombinant Lck in presence of 10 mM ATP |
Bioorg Med Chem Lett 16: 4257-61 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.072 BindingDB Entry DOI: 10.7270/Q22V2FQD |
More data for this Ligand-Target Pair | |
Proto-oncogene tyrosine-protein kinase Src
(Homo sapiens (Human)) | BDBM50188343
(4-(2,6-dichloro-phenyl)-8-[4-(2-diethylamino-ethox...)Show SMILES CCN(CC)CCOc1ccc(Nc2ncc3C=C(N4N(CCC4=O)c3n2)c2c(Cl)cccc2Cl)cc1 |c:17| Show InChI InChI=1S/C27H28Cl2N6O2/c1-3-33(4-2)14-15-37-20-10-8-19(9-11-20)31-27-30-17-18-16-23(25-21(28)6-5-7-22(25)29)35-24(36)12-13-34(35)26(18)32-27/h5-11,16-17H,3-4,12-15H2,1-2H3,(H,30,31,32) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 3 | n/a | n/a | n/a | n/a | n/a | n/a |
Procter and Gamble Pharmaceuticals
Curated by ChEMBL
| Assay Description Inhibition of human recombinant Src in presence of 10 mM ATP |
Bioorg Med Chem Lett 16: 4257-61 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.072 BindingDB Entry DOI: 10.7270/Q22V2FQD |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50188348
(4-(2-chloro-5-hydroxy-phenyl)-8-(4-dimethylamino-p...)Show SMILES CN(C)c1ccc(Nc2ncc3C=C(N4N(CCC4=O)c3n2)c2cc(O)ccc2Cl)cc1 |c:12| Show InChI InChI=1S/C23H21ClN6O2/c1-28(2)16-5-3-15(4-6-16)26-23-25-13-14-11-20(18-12-17(31)7-8-19(18)24)30-21(32)9-10-29(30)22(14)27-23/h3-8,11-13,31H,9-10H2,1-2H3,(H,25,26,27) | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 10 | n/a | n/a | n/a | n/a | n/a | n/a |
Procter and Gamble Pharmaceuticals
Curated by ChEMBL
| Assay Description Inhibition of human recombinant Lck in presence of 10 mM ATP |
Bioorg Med Chem Lett 16: 4257-61 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.072 BindingDB Entry DOI: 10.7270/Q22V2FQD |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50188357
(4-(2,6-dichloro-phenyl)-8-[4-(2-dimethylamino-ethy...)Show SMILES CN(C)CCc1ccc(Nc2ncc3C=C(N4N(CCC4=O)c3n2)c2c(Cl)cccc2Cl)cc1 |c:14| Show InChI InChI=1S/C25H24Cl2N6O/c1-31(2)12-10-16-6-8-18(9-7-16)29-25-28-15-17-14-21(23-19(26)4-3-5-20(23)27)33-22(34)11-13-32(33)24(17)30-25/h3-9,14-15H,10-13H2,1-2H3,(H,28,29,30) | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 21 | n/a | n/a | n/a | n/a | n/a | n/a |
Procter and Gamble Pharmaceuticals
Curated by ChEMBL
| Assay Description Inhibition of human recombinant Lck in presence of 10 mM ATP |
Bioorg Med Chem Lett 16: 4257-61 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.072 BindingDB Entry DOI: 10.7270/Q22V2FQD |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50188352
(4-(2,6-dichloro-phenyl)-8-(4-dimethylamino-phenyla...)Show SMILES CN(C)c1ccc(Nc2ncc3C=C(N4N(CCC4=O)c3n2)c2c(Cl)cccc2Cl)cc1 |c:12| Show InChI InChI=1S/C23H20Cl2N6O/c1-29(2)16-8-6-15(7-9-16)27-23-26-13-14-12-19(21-17(24)4-3-5-18(21)25)31-20(32)10-11-30(31)22(14)28-23/h3-9,12-13H,10-11H2,1-2H3,(H,26,27,28) | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 26 | n/a | n/a | n/a | n/a | n/a | n/a |
Procter and Gamble Pharmaceuticals
Curated by ChEMBL
| Assay Description Inhibition of human recombinant Lck in presence of 10 mM ATP |
Bioorg Med Chem Lett 16: 4257-61 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.072 BindingDB Entry DOI: 10.7270/Q22V2FQD |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50188347
(4-(2,6-dichloro-phenyl)-8-(4-diethylamino-phenylam...)Show SMILES CCN(CC)c1ccc(Nc2ncc3C=C(N4N(CCC4=O)c3n2)c2c(Cl)cccc2Cl)cc1 |c:14| Show InChI InChI=1S/C25H24Cl2N6O/c1-3-31(4-2)18-10-8-17(9-11-18)29-25-28-15-16-14-21(23-19(26)6-5-7-20(23)27)33-22(34)12-13-32(33)24(16)30-25/h5-11,14-15H,3-4,12-13H2,1-2H3,(H,28,29,30) | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 43 | n/a | n/a | n/a | n/a | n/a | n/a |
Procter and Gamble Pharmaceuticals
Curated by ChEMBL
| Assay Description Inhibition of human recombinant Lck in presence of 10 mM ATP |
Bioorg Med Chem Lett 16: 4257-61 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.072 BindingDB Entry DOI: 10.7270/Q22V2FQD |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50188340
(4-(2-chloro-5-hydroxy-phenyl)-8-[4-(4-methyl-piper...)Show SMILES CN1CCN(CC1)c1ccc(Nc2ncc3C=C(N4N(CCC4=O)c3n2)c2cc(O)ccc2Cl)cc1 |c:17| Show InChI InChI=1S/C26H26ClN7O2/c1-31-10-12-32(13-11-31)19-4-2-18(3-5-19)29-26-28-16-17-14-23(21-15-20(35)6-7-22(21)27)34-24(36)8-9-33(34)25(17)30-26/h2-7,14-16,35H,8-13H2,1H3,(H,28,29,30) | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 47 | n/a | n/a | n/a | n/a | n/a | n/a |
Procter and Gamble Pharmaceuticals
Curated by ChEMBL
| Assay Description Inhibition of human recombinant Lck in presence of 10 mM ATP |
Bioorg Med Chem Lett 16: 4257-61 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.072 BindingDB Entry DOI: 10.7270/Q22V2FQD |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase HCK
(Homo sapiens (Human)) | BDBM50188343
(4-(2,6-dichloro-phenyl)-8-[4-(2-diethylamino-ethox...)Show SMILES CCN(CC)CCOc1ccc(Nc2ncc3C=C(N4N(CCC4=O)c3n2)c2c(Cl)cccc2Cl)cc1 |c:17| Show InChI InChI=1S/C27H28Cl2N6O2/c1-3-33(4-2)14-15-37-20-10-8-19(9-11-20)31-27-30-17-18-16-23(25-21(28)6-5-7-22(25)29)35-24(36)12-13-34(35)26(18)32-27/h5-11,16-17H,3-4,12-15H2,1-2H3,(H,30,31,32) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 48 | n/a | n/a | n/a | n/a | n/a | n/a |
Procter and Gamble Pharmaceuticals
Curated by ChEMBL
| Assay Description Inhibition of human recombinant Hck in presence of 10 mM ATP |
Bioorg Med Chem Lett 16: 4257-61 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.072 BindingDB Entry DOI: 10.7270/Q22V2FQD |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50188356
(4-(2,6-dichloro-phenyl)-8-(4-methoxy-phenylamino)-...)Show SMILES COc1ccc(Nc2ncc3C=C(N4N(CCC4=O)c3n2)c2c(Cl)cccc2Cl)cc1 |c:11| Show InChI InChI=1S/C22H17Cl2N5O2/c1-31-15-7-5-14(6-8-15)26-22-25-12-13-11-18(20-16(23)3-2-4-17(20)24)29-19(30)9-10-28(29)21(13)27-22/h2-8,11-12H,9-10H2,1H3,(H,25,26,27) | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 71 | n/a | n/a | n/a | n/a | n/a | n/a |
Procter and Gamble Pharmaceuticals
Curated by ChEMBL
| Assay Description Inhibition of human recombinant Lck in presence of 10 mM ATP |
Bioorg Med Chem Lett 16: 4257-61 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.072 BindingDB Entry DOI: 10.7270/Q22V2FQD |
More data for this Ligand-Target Pair | |
Proto-oncogene tyrosine-protein kinase Src
(Homo sapiens (Human)) | BDBM50188342
(4-(2,6-dichloro-phenyl)-8-(4-morpholin-4-yl-phenyl...)Show SMILES Clc1cccc(Cl)c1C1=Cc2cnc(Nc3ccc(cc3)N3CCOCC3)nc2N2CCC(=O)N12 |t:9| Show InChI InChI=1S/C25H22Cl2N6O2/c26-19-2-1-3-20(27)23(19)21-14-16-15-28-25(30-24(16)32-9-8-22(34)33(21)32)29-17-4-6-18(7-5-17)31-10-12-35-13-11-31/h1-7,14-15H,8-13H2,(H,28,29,30) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 104 | n/a | n/a | n/a | n/a | n/a | n/a |
Procter and Gamble Pharmaceuticals
Curated by ChEMBL
| Assay Description Inhibition of human recombinant Src in presence of 10 mM ATP |
Bioorg Med Chem Lett 16: 4257-61 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.072 BindingDB Entry DOI: 10.7270/Q22V2FQD |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50188349
(4-(2,6-dichloro-phenyl)-8-(4-fluoro-phenylamino)-1...)Show SMILES Fc1ccc(Nc2ncc3C=C(N4N(CCC4=O)c3n2)c2c(Cl)cccc2Cl)cc1 |c:10| Show InChI InChI=1S/C21H14Cl2FN5O/c22-15-2-1-3-16(23)19(15)17-10-12-11-25-21(26-14-6-4-13(24)5-7-14)27-20(12)28-9-8-18(30)29(17)28/h1-7,10-11H,8-9H2,(H,25,26,27) | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 124 | n/a | n/a | n/a | n/a | n/a | n/a |
Procter and Gamble Pharmaceuticals
Curated by ChEMBL
| Assay Description Inhibition of human recombinant Lck in presence of 10 mM ATP |
Bioorg Med Chem Lett 16: 4257-61 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.072 BindingDB Entry DOI: 10.7270/Q22V2FQD |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50188350
(4-[4-(2,6-dichloro-phenyl)-3-oxo-2,3-dihydro-1H-3a...)Show SMILES COC(=O)c1ccc(Nc2ncc3C=C(N4N(CCC4=O)c3n2)c2c(Cl)cccc2Cl)cc1 |c:13| Show InChI InChI=1S/C23H17Cl2N5O3/c1-33-22(32)13-5-7-15(8-6-13)27-23-26-12-14-11-18(20-16(24)3-2-4-17(20)25)30-19(31)9-10-29(30)21(14)28-23/h2-8,11-12H,9-10H2,1H3,(H,26,27,28) | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 143 | n/a | n/a | n/a | n/a | n/a | n/a |
Procter and Gamble Pharmaceuticals
Curated by ChEMBL
| Assay Description Inhibition of human recombinant Lck in presence of 10 mM ATP |
Bioorg Med Chem Lett 16: 4257-61 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.072 BindingDB Entry DOI: 10.7270/Q22V2FQD |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase HCK
(Homo sapiens (Human)) | BDBM50188342
(4-(2,6-dichloro-phenyl)-8-(4-morpholin-4-yl-phenyl...)Show SMILES Clc1cccc(Cl)c1C1=Cc2cnc(Nc3ccc(cc3)N3CCOCC3)nc2N2CCC(=O)N12 |t:9| Show InChI InChI=1S/C25H22Cl2N6O2/c26-19-2-1-3-20(27)23(19)21-14-16-15-28-25(30-24(16)32-9-8-22(34)33(21)32)29-17-4-6-18(7-5-17)31-10-12-35-13-11-31/h1-7,14-15H,8-13H2,(H,28,29,30) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 160 | n/a | n/a | n/a | n/a | n/a | n/a |
Procter and Gamble Pharmaceuticals
Curated by ChEMBL
| Assay Description Inhibition of human recombinant Hck in presence of 10 mM ATP |
Bioorg Med Chem Lett 16: 4257-61 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.072 BindingDB Entry DOI: 10.7270/Q22V2FQD |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50188355
(4-(2,6-dichloro-phenyl)-8-(3-methoxy-phenylamino)-...)Show SMILES COc1cccc(Nc2ncc3C=C(N4N(CCC4=O)c3n2)c2c(Cl)cccc2Cl)c1 |c:12| Show InChI InChI=1S/C22H17Cl2N5O2/c1-31-15-5-2-4-14(11-15)26-22-25-12-13-10-18(20-16(23)6-3-7-17(20)24)29-19(30)8-9-28(29)21(13)27-22/h2-7,10-12H,8-9H2,1H3,(H,25,26,27) | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 179 | n/a | n/a | n/a | n/a | n/a | n/a |
Procter and Gamble Pharmaceuticals
Curated by ChEMBL
| Assay Description Inhibition of human recombinant Lck in presence of 10 mM ATP |
Bioorg Med Chem Lett 16: 4257-61 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.072 BindingDB Entry DOI: 10.7270/Q22V2FQD |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50188353
(4-(2,6-dichloro-phenyl)-8-phenylamino-1,2-dihydro-...)Show SMILES Clc1cccc(Cl)c1C1=Cc2cnc(Nc3ccccc3)nc2N2CCC(=O)N12 |t:9| Show InChI InChI=1S/C21H15Cl2N5O/c22-15-7-4-8-16(23)19(15)17-11-13-12-24-21(25-14-5-2-1-3-6-14)26-20(13)27-10-9-18(29)28(17)27/h1-8,11-12H,9-10H2,(H,24,25,26) | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 182 | n/a | n/a | n/a | n/a | n/a | n/a |
Procter and Gamble Pharmaceuticals
Curated by ChEMBL
| Assay Description Inhibition of human recombinant Lck in presence of 10 mM ATP |
Bioorg Med Chem Lett 16: 4257-61 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.072 BindingDB Entry DOI: 10.7270/Q22V2FQD |
More data for this Ligand-Target Pair | |
Proto-oncogene tyrosine-protein kinase Src
(Homo sapiens (Human)) | BDBM50188348
(4-(2-chloro-5-hydroxy-phenyl)-8-(4-dimethylamino-p...)Show SMILES CN(C)c1ccc(Nc2ncc3C=C(N4N(CCC4=O)c3n2)c2cc(O)ccc2Cl)cc1 |c:12| Show InChI InChI=1S/C23H21ClN6O2/c1-28(2)16-5-3-15(4-6-16)26-23-25-13-14-11-20(18-12-17(31)7-8-19(18)24)30-21(32)9-10-29(30)22(14)27-23/h3-8,11-13,31H,9-10H2,1-2H3,(H,25,26,27) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 273 | n/a | n/a | n/a | n/a | n/a | n/a |
Procter and Gamble Pharmaceuticals
Curated by ChEMBL
| Assay Description Inhibition of human recombinant Src in presence of 10 mM ATP |
Bioorg Med Chem Lett 16: 4257-61 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.072 BindingDB Entry DOI: 10.7270/Q22V2FQD |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50188354
(4-(2,6-dichloro-phenyl)-8-(4-ethoxy-phenylamino)-1...)Show SMILES CCOc1ccc(Nc2ncc3C=C(N4N(CCC4=O)c3n2)c2c(Cl)cccc2Cl)cc1 |c:12| Show InChI InChI=1S/C23H19Cl2N5O2/c1-2-32-16-8-6-15(7-9-16)27-23-26-13-14-12-19(21-17(24)4-3-5-18(21)25)30-20(31)10-11-29(30)22(14)28-23/h3-9,12-13H,2,10-11H2,1H3,(H,26,27,28) | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 285 | n/a | n/a | n/a | n/a | n/a | n/a |
Procter and Gamble Pharmaceuticals
Curated by ChEMBL
| Assay Description Inhibition of human recombinant Lck in presence of 10 mM ATP |
Bioorg Med Chem Lett 16: 4257-61 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.072 BindingDB Entry DOI: 10.7270/Q22V2FQD |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase HCK
(Homo sapiens (Human)) | BDBM50188340
(4-(2-chloro-5-hydroxy-phenyl)-8-[4-(4-methyl-piper...)Show SMILES CN1CCN(CC1)c1ccc(Nc2ncc3C=C(N4N(CCC4=O)c3n2)c2cc(O)ccc2Cl)cc1 |c:17| Show InChI InChI=1S/C26H26ClN7O2/c1-31-10-12-32(13-11-31)19-4-2-18(3-5-19)29-26-28-16-17-14-23(21-15-20(35)6-7-22(21)27)34-24(36)8-9-33(34)25(17)30-26/h2-7,14-16,35H,8-13H2,1H3,(H,28,29,30) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 456 | n/a | n/a | n/a | n/a | n/a | n/a |
Procter and Gamble Pharmaceuticals
Curated by ChEMBL
| Assay Description Inhibition of human recombinant Hck in presence of 10 mM ATP |
Bioorg Med Chem Lett 16: 4257-61 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.072 BindingDB Entry DOI: 10.7270/Q22V2FQD |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase HCK
(Homo sapiens (Human)) | BDBM50188348
(4-(2-chloro-5-hydroxy-phenyl)-8-(4-dimethylamino-p...)Show SMILES CN(C)c1ccc(Nc2ncc3C=C(N4N(CCC4=O)c3n2)c2cc(O)ccc2Cl)cc1 |c:12| Show InChI InChI=1S/C23H21ClN6O2/c1-28(2)16-5-3-15(4-6-16)26-23-25-13-14-11-20(18-12-17(31)7-8-19(18)24)30-21(32)9-10-29(30)22(14)27-23/h3-8,11-13,31H,9-10H2,1-2H3,(H,25,26,27) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 546 | n/a | n/a | n/a | n/a | n/a | n/a |
Procter and Gamble Pharmaceuticals
Curated by ChEMBL
| Assay Description Inhibition of human recombinant Hck in presence of 10 mM ATP |
Bioorg Med Chem Lett 16: 4257-61 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.072 BindingDB Entry DOI: 10.7270/Q22V2FQD |
More data for this Ligand-Target Pair | |
Proto-oncogene tyrosine-protein kinase Src
(Homo sapiens (Human)) | BDBM50188340
(4-(2-chloro-5-hydroxy-phenyl)-8-[4-(4-methyl-piper...)Show SMILES CN1CCN(CC1)c1ccc(Nc2ncc3C=C(N4N(CCC4=O)c3n2)c2cc(O)ccc2Cl)cc1 |c:17| Show InChI InChI=1S/C26H26ClN7O2/c1-31-10-12-32(13-11-31)19-4-2-18(3-5-19)29-26-28-16-17-14-23(21-15-20(35)6-7-22(21)27)34-24(36)8-9-33(34)25(17)30-26/h2-7,14-16,35H,8-13H2,1H3,(H,28,29,30) | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 764 | n/a | n/a | n/a | n/a | n/a | n/a |
Procter and Gamble Pharmaceuticals
Curated by ChEMBL
| Assay Description Inhibition of human recombinant Src in presence of 10 mM ATP |
Bioorg Med Chem Lett 16: 4257-61 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.072 BindingDB Entry DOI: 10.7270/Q22V2FQD |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50188346
(4-(2,6-dichloro-phenyl)-8-methylamino-1,2-dihydro-...)Show SMILES CNc1ncc2C=C(N3N(CCC3=O)c2n1)c1c(Cl)cccc1Cl |c:6| Show InChI InChI=1S/C16H13Cl2N5O/c1-19-16-20-8-9-7-12(14-10(17)3-2-4-11(14)18)23-13(24)5-6-22(23)15(9)21-16/h2-4,7-8H,5-6H2,1H3,(H,19,20,21) | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 2.81E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Procter and Gamble Pharmaceuticals
Curated by ChEMBL
| Assay Description Inhibition of human recombinant Lck in presence of 10 mM ATP |
Bioorg Med Chem Lett 16: 4257-61 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.072 BindingDB Entry DOI: 10.7270/Q22V2FQD |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50188351
(4-(2-chloro-5-methoxy-phenyl)-8-(4-dimethylamino-p...)Show SMILES COc1ccc(Cl)c(c1)C1=Cc2cnc(Nc3ccc(cc3)N(C)C)nc2N2CCC(=O)N12 |t:10| Show InChI InChI=1S/C24H23ClN6O2/c1-29(2)17-6-4-16(5-7-17)27-24-26-14-15-12-21(19-13-18(33-3)8-9-20(19)25)31-22(32)10-11-30(31)23(15)28-24/h4-9,12-14H,10-11H2,1-3H3,(H,26,27,28) | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 2.84E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Procter and Gamble Pharmaceuticals
Curated by ChEMBL
| Assay Description Inhibition of human recombinant Lck in presence of 10 mM ATP |
Bioorg Med Chem Lett 16: 4257-61 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.072 BindingDB Entry DOI: 10.7270/Q22V2FQD |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50188344
(3-(2,6-dichlorophenyl)-N-(4-fluorophenyl)-1,2-dime...)Show SMILES CN1N(C)c2nc(Nc3ccc(F)cc3)ncc2C=C1c1c(Cl)cccc1Cl |c:20| Show InChI InChI=1S/C20H16Cl2FN5/c1-27-17(18-15(21)4-3-5-16(18)22)10-12-11-24-20(26-19(12)28(27)2)25-14-8-6-13(23)7-9-14/h3-11H,1-2H3,(H,24,25,26) | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 3.20E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Procter and Gamble Pharmaceuticals
Curated by ChEMBL
| Assay Description Inhibition of human recombinant Lck in presence of 10 mM ATP |
Bioorg Med Chem Lett 16: 4257-61 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.072 BindingDB Entry DOI: 10.7270/Q22V2FQD |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50188341
(4-(2-chloro-5-methoxy-phenyl)-8-(4-fluoro-phenylam...)Show SMILES COc1ccc(Cl)c(c1)C1=Cc2cnc(Nc3ccc(F)cc3)nc2N2CCC(=O)N12 |t:10| Show InChI InChI=1S/C22H17ClFN5O2/c1-31-16-6-7-18(23)17(11-16)19-10-13-12-25-22(26-15-4-2-14(24)3-5-15)27-21(13)28-9-8-20(30)29(19)28/h2-7,10-12H,8-9H2,1H3,(H,25,26,27) | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 4.80E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Procter and Gamble Pharmaceuticals
Curated by ChEMBL
| Assay Description Inhibition of human recombinant Lck in presence of 10 mM ATP |
Bioorg Med Chem Lett 16: 4257-61 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.072 BindingDB Entry DOI: 10.7270/Q22V2FQD |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50188345
(4-(2,6-dichloro-phenyl)-8-(2-methoxy-phenylamino)-...)Show SMILES COc1ccccc1Nc1ncc2C=C(N3N(CCC3=O)c2n1)c1c(Cl)cccc1Cl |c:14| Show InChI InChI=1S/C22H17Cl2N5O2/c1-31-18-8-3-2-7-16(18)26-22-25-12-13-11-17(20-14(23)5-4-6-15(20)24)29-19(30)9-10-28(29)21(13)27-22/h2-8,11-12H,9-10H2,1H3,(H,25,26,27) | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 7.27E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Procter and Gamble Pharmaceuticals
Curated by ChEMBL
| Assay Description Inhibition of human recombinant Lck in presence of 10 mM ATP |
Bioorg Med Chem Lett 16: 4257-61 (2006)
Article DOI: 10.1016/j.bmcl.2006.05.072 BindingDB Entry DOI: 10.7270/Q22V2FQD |
More data for this Ligand-Target Pair | |