Compile Data Set for Download or QSAR

Found 82 hits Enz. Inhib. hit(s) with all data for entry = 50019209   

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))	BDBM50202759 (CHEMBL231720 | N-(4-(4-amino-1-methyl-1H-pyrazolo[...) Show SMILES COc1cc(ccc1NC(=O)c1cc2ccccc2n1C)-c1nn(C)c2ncnc(N)c12 Show InChI InChI=1S/C23H21N7O2/c1-29-16-7-5-4-6-13(16)10-17(29)23(31)27-15-9-8-14(11-18(15)32-3)20-19-21(24)25-12-26-22(19)30(2)28-20/h4-12H,1-3H3,(H,27,31)(H2,24,25,26)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	31	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Bioresearch Center Curated by ChEMBL					Assay Description Inhibition of Lck				Bioorg Med Chem Lett 17: 1167-71 (2007) Article DOI: 10.1016/j.bmcl.2006.12.035 BindingDB Entry DOI: 10.7270/Q24Q7TN6
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50202737 (CHEMBL395665 | N-(4-(4-amino-7-(3-((1r,4r)-4-amino...) Show SMILES COc1cc(ccc1NC(=O)c1cc2ccccc2n1C)-c1csc2c(\C=C\CN[C@H]3CC[C@H](N)CC3)cnc(N)c12 |wU:30.32,wD:33.36,(5.61,-23.77,;4.15,-23.29,;3.01,-24.32,;1.54,-23.84,;.4,-24.87,;.73,-26.38,;2.18,-26.85,;3.33,-25.82,;4.78,-26.3,;5.1,-27.8,;3.96,-28.84,;6.57,-28.28,;7.04,-29.76,;8.59,-29.75,;9.62,-30.9,;11.13,-30.57,;11.61,-29.11,;10.57,-27.96,;9.07,-28.28,;7.83,-27.37,;7.83,-25.83,;-1.07,-24.39,;-2.31,-25.31,;-3.56,-24.4,;-3.08,-22.94,;-3.85,-21.62,;-5.39,-21.62,;-6.16,-20.29,;-7.7,-20.3,;-8.47,-18.96,;-7.71,-17.63,;-8.47,-16.3,;-7.7,-14.97,;-6.16,-14.97,;-5.39,-13.64,;-5.4,-16.3,;-6.16,-17.63,;-3.09,-20.3,;-1.55,-20.29,;-.79,-21.62,;.75,-21.62,;-1.55,-22.94,)| Show InChI InChI=1S/C33H36N6O2S/c1-39-27-8-4-3-6-21(27)16-28(39)33(40)38-26-14-9-20(17-29(26)41-2)25-19-42-31-22(18-37-32(35)30(25)31)7-5-15-36-24-12-10-23(34)11-13-24/h3-9,14,16-19,23-24,36H,10-13,15,34H2,1-2H3,(H2,35,37)(H,38,40)/b7-5+/t23-,24-	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	110	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Bioresearch Center Curated by ChEMBL					Assay Description Inhibition of Lck				Bioorg Med Chem Lett 17: 1167-71 (2007) Article DOI: 10.1016/j.bmcl.2006.12.035 BindingDB Entry DOI: 10.7270/Q24Q7TN6
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50202757 (CHEMBL396359 | N-(4-(4-amino-7-(3-oxo-3-(piperidin...) Show SMILES COc1cc(ccc1NC(=O)c1cc2ccccc2n1C)-c1csc2C(CN=C(N)c12)C=CC(=O)NC1CCNCC1 |w:31.35,t:30| Show InChI InChI=1S/C32H34N6O3S/c1-38-25-6-4-3-5-20(25)15-26(38)32(40)37-24-9-7-19(16-27(24)41-2)23-18-42-30-21(17-35-31(33)29(23)30)8-10-28(39)36-22-11-13-34-14-12-22/h3-10,15-16,18,21-22,34H,11-14,17H2,1-2H3,(H2,33,35)(H,36,39)(H,37,40)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	130	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Bioresearch Center Curated by ChEMBL					Assay Description Inhibition of Lck				Bioorg Med Chem Lett 17: 1167-71 (2007) Article DOI: 10.1016/j.bmcl.2006.12.035 BindingDB Entry DOI: 10.7270/Q24Q7TN6
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50202733 (4-amino-N-(2-(dimethylamino)ethyl)-3-(3-methoxy-4-...) Show SMILES COc1cc(ccc1NC(=O)c1cc2ccccc2n1C)-c1csc2c(cnc(N)c12)C(=O)NCCN(C)C Show InChI InChI=1S/C29H30N6O3S/c1-34(2)12-11-31-28(36)19-15-32-27(30)25-20(16-39-26(19)25)17-9-10-21(24(14-17)38-4)33-29(37)23-13-18-7-5-6-8-22(18)35(23)3/h5-10,13-16H,11-12H2,1-4H3,(H2,30,32)(H,31,36)(H,33,37)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	140	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Bioresearch Center Curated by ChEMBL					Assay Description Inhibition of Lck				Bioorg Med Chem Lett 17: 1167-71 (2007) Article DOI: 10.1016/j.bmcl.2006.12.035 BindingDB Entry DOI: 10.7270/Q24Q7TN6
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50202739 (CHEMBL395664 | N-(4-(4-amino-7-(3-(piperidin-4-yla...) Show SMILES COc1cc(ccc1NC(=O)c1cc2ccccc2n1C)-c1csc2c(\C=C\CNC3CCNCC3)cnc(N)c12 Show InChI InChI=1S/C32H34N6O2S/c1-38-26-8-4-3-6-21(26)16-27(38)32(39)37-25-10-9-20(17-28(25)40-2)24-19-41-30-22(18-36-31(33)29(24)30)7-5-13-35-23-11-14-34-15-12-23/h3-10,16-19,23,34-35H,11-15H2,1-2H3,(H2,33,36)(H,37,39)/b7-5+	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	190	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Bioresearch Center Curated by ChEMBL					Assay Description Inhibition of Lck				Bioorg Med Chem Lett 17: 1167-71 (2007) Article DOI: 10.1016/j.bmcl.2006.12.035 BindingDB Entry DOI: 10.7270/Q24Q7TN6
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50202741 (CHEMBL233958 | N-(4-(4-amino-7-(3-(4-hydroxypiperi...) Show SMILES COc1cc(ccc1NC(=O)c1cc2ccccc2n1C)-c1csc2c(\C=C\CN3CCC(O)CC3)cnc(N)c12 Show InChI InChI=1S/C32H33N5O3S/c1-36-26-8-4-3-6-21(26)16-27(36)32(39)35-25-10-9-20(17-28(25)40-2)24-19-41-30-22(18-34-31(33)29(24)30)7-5-13-37-14-11-23(38)12-15-37/h3-10,16-19,23,38H,11-15H2,1-2H3,(H2,33,34)(H,35,39)/b7-5+	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	210	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Bioresearch Center Curated by ChEMBL					Assay Description Inhibition of Lck				Bioorg Med Chem Lett 17: 1167-71 (2007) Article DOI: 10.1016/j.bmcl.2006.12.035 BindingDB Entry DOI: 10.7270/Q24Q7TN6
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50202738 (CHEMBL232127 | trans-N-(4-(4-amino-7-(3-aminoprop-...) Show SMILES COc1cc(ccc1NC(=O)c1cc2ccccc2n1C)-c1csc2c(\C=C\CN)cnc(N)c12 Show InChI InChI=1S/C27H25N5O2S/c1-32-21-8-4-3-6-17(21)12-22(32)27(33)31-20-10-9-16(13-23(20)34-2)19-15-35-25-18(7-5-11-28)14-30-26(29)24(19)25/h3-10,12-15H,11,28H2,1-2H3,(H2,29,30)(H,31,33)/b7-5+	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	230	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Bioresearch Center Curated by ChEMBL					Assay Description Inhibition of Lck				Bioorg Med Chem Lett 17: 1167-71 (2007) Article DOI: 10.1016/j.bmcl.2006.12.035 BindingDB Entry DOI: 10.7270/Q24Q7TN6
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50202745 (4-amino-3-(3-methoxy-4-(1-methyl-1H-indole-2-carbo...) Show SMILES COc1cc(ccc1NC(=O)c1cc2ccccc2n1C)-c1csc2c(cnc(N)c12)C(=O)NCCN1CCCC1 Show InChI InChI=1S/C31H32N6O3S/c1-36-24-8-4-3-7-20(24)15-25(36)31(39)35-23-10-9-19(16-26(23)40-2)22-18-41-28-21(17-34-29(32)27(22)28)30(38)33-11-14-37-12-5-6-13-37/h3-4,7-10,15-18H,5-6,11-14H2,1-2H3,(H2,32,34)(H,33,38)(H,35,39)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	240	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Bioresearch Center Curated by ChEMBL					Assay Description Inhibition of Lck				Bioorg Med Chem Lett 17: 1167-71 (2007) Article DOI: 10.1016/j.bmcl.2006.12.035 BindingDB Entry DOI: 10.7270/Q24Q7TN6
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50202754 (CHEMBL395662 | N-(4-(4-amino-7-(3-(4-methylpiperaz...) Show SMILES COc1cc(ccc1NC(=O)c1cc2ccccc2n1C)-c1csc2c(\C=C\CN3CCN(C)CC3)cnc(N)c12 Show InChI InChI=1S/C32H34N6O2S/c1-36-13-15-38(16-14-36)12-6-8-23-19-34-31(33)29-24(20-41-30(23)29)21-10-11-25(28(18-21)40-3)35-32(39)27-17-22-7-4-5-9-26(22)37(27)2/h4-11,17-20H,12-16H2,1-3H3,(H2,33,34)(H,35,39)/b8-6+	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	290	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Bioresearch Center Curated by ChEMBL					Assay Description Inhibition of Lck				Bioorg Med Chem Lett 17: 1167-71 (2007) Article DOI: 10.1016/j.bmcl.2006.12.035 BindingDB Entry DOI: 10.7270/Q24Q7TN6
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50202734 (CHEMBL232542 | N-(4-(4-amino-7-(3-(diethylamino)pr...) Show SMILES CCN(CC)C\C=C\c1cnc(N)c2c(csc12)-c1ccc(NC(=O)c2cc3ccccc3n2C)c(OC)c1 Show InChI InChI=1S/C31H33N5O2S/c1-5-36(6-2)15-9-11-22-18-33-30(32)28-23(19-39-29(22)28)20-13-14-24(27(17-20)38-4)34-31(37)26-16-21-10-7-8-12-25(21)35(26)3/h7-14,16-19H,5-6,15H2,1-4H3,(H2,32,33)(H,34,37)/b11-9+	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	290	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Bioresearch Center Curated by ChEMBL					Assay Description Inhibition of Lck				Bioorg Med Chem Lett 17: 1167-71 (2007) Article DOI: 10.1016/j.bmcl.2006.12.035 BindingDB Entry DOI: 10.7270/Q24Q7TN6
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50202744 (4-amino-3-(3-methoxy-4-(1-methyl-1H-indole-2-carbo...) Show SMILES COc1cc(ccc1NC(=O)c1cc2ccccc2n1C)-c1csc2c(cnc(N)c12)C(N)=O Show InChI InChI=1S/C25H21N5O3S/c1-30-18-6-4-3-5-14(18)9-19(30)25(32)29-17-8-7-13(10-20(17)33-2)16-12-34-22-15(24(27)31)11-28-23(26)21(16)22/h3-12H,1-2H3,(H2,26,28)(H2,27,31)(H,29,32)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	380	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Bioresearch Center Curated by ChEMBL					Assay Description Inhibition of Lck				Bioorg Med Chem Lett 17: 1167-71 (2007) Article DOI: 10.1016/j.bmcl.2006.12.035 BindingDB Entry DOI: 10.7270/Q24Q7TN6
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50202735 (CHEMBL395666 | N-(4-(4-amino-7-(3-((1s,4s)-4-amino...) Show SMILES COc1cc(ccc1NC(=O)c1cc2ccccc2n1C)-c1csc2c(\C=C\CN[C@@H]3CC[C@H](N)CC3)cnc(N)c12 |wU:30.32,33.36,(28.87,-24.7,;27.4,-24.22,;26.26,-25.25,;24.79,-24.77,;23.65,-25.8,;23.98,-27.31,;25.43,-27.78,;26.58,-26.75,;28.03,-27.23,;28.36,-28.73,;27.21,-29.77,;29.82,-29.21,;30.29,-30.69,;31.84,-30.68,;32.87,-31.82,;34.38,-31.5,;34.86,-30.04,;33.82,-28.89,;32.32,-29.21,;31.08,-28.3,;31.08,-26.76,;22.18,-25.32,;20.94,-26.24,;19.69,-25.33,;20.17,-23.87,;19.4,-22.55,;17.86,-22.55,;17.09,-21.22,;15.55,-21.23,;14.78,-19.89,;15.54,-18.56,;17.09,-18.56,;17.85,-17.23,;17.09,-15.9,;17.86,-14.57,;15.55,-15.9,;14.78,-17.23,;20.16,-21.22,;21.7,-21.22,;22.47,-22.55,;24.01,-22.55,;21.7,-23.87,)| Show InChI InChI=1S/C33H36N6O2S/c1-39-27-8-4-3-6-21(27)16-28(39)33(40)38-26-14-9-20(17-29(26)41-2)25-19-42-31-22(18-37-32(35)30(25)31)7-5-15-36-24-12-10-23(34)11-13-24/h3-9,14,16-19,23-24,36H,10-13,15,34H2,1-2H3,(H2,35,37)(H,38,40)/b7-5+/t23-,24+	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	480	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Bioresearch Center Curated by ChEMBL					Assay Description Inhibition of Lck				Bioorg Med Chem Lett 17: 1167-71 (2007) Article DOI: 10.1016/j.bmcl.2006.12.035 BindingDB Entry DOI: 10.7270/Q24Q7TN6
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50202736 (CHEMBL231930 | trans-N-(4-(4-amino-7-(3-amino-3-ox...) Show SMILES COc1cc(ccc1NC(=O)c1cc2ccccc2n1C)-c1csc2c(\C=C\C(N)=O)cnc(N)c12 Show InChI InChI=1S/C27H23N5O3S/c1-32-20-6-4-3-5-16(20)11-21(32)27(34)31-19-9-7-15(12-22(19)35-2)18-14-36-25-17(8-10-23(28)33)13-30-26(29)24(18)25/h3-14H,1-2H3,(H2,28,33)(H2,29,30)(H,31,34)/b10-8+	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	541	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Bioresearch Center Curated by ChEMBL					Assay Description Inhibition of Lck				Bioorg Med Chem Lett 17: 1167-71 (2007) Article DOI: 10.1016/j.bmcl.2006.12.035 BindingDB Entry DOI: 10.7270/Q24Q7TN6
					More data for this Ligand-Target Pair
Angiopoietin-1 receptor (Homo sapiens (Human))	BDBM50202735 (CHEMBL395666 | N-(4-(4-amino-7-(3-((1s,4s)-4-amino...) Show SMILES COc1cc(ccc1NC(=O)c1cc2ccccc2n1C)-c1csc2c(\C=C\CN[C@@H]3CC[C@H](N)CC3)cnc(N)c12 |wU:30.32,33.36,(28.87,-24.7,;27.4,-24.22,;26.26,-25.25,;24.79,-24.77,;23.65,-25.8,;23.98,-27.31,;25.43,-27.78,;26.58,-26.75,;28.03,-27.23,;28.36,-28.73,;27.21,-29.77,;29.82,-29.21,;30.29,-30.69,;31.84,-30.68,;32.87,-31.82,;34.38,-31.5,;34.86,-30.04,;33.82,-28.89,;32.32,-29.21,;31.08,-28.3,;31.08,-26.76,;22.18,-25.32,;20.94,-26.24,;19.69,-25.33,;20.17,-23.87,;19.4,-22.55,;17.86,-22.55,;17.09,-21.22,;15.55,-21.23,;14.78,-19.89,;15.54,-18.56,;17.09,-18.56,;17.85,-17.23,;17.09,-15.9,;17.86,-14.57,;15.55,-15.9,;14.78,-17.23,;20.16,-21.22,;21.7,-21.22,;22.47,-22.55,;24.01,-22.55,;21.7,-23.87,)| Show InChI InChI=1S/C33H36N6O2S/c1-39-27-8-4-3-6-21(27)16-28(39)33(40)38-26-14-9-20(17-29(26)41-2)25-19-42-31-22(18-37-32(35)30(25)31)7-5-15-36-24-12-10-23(34)11-13-24/h3-9,14,16-19,23-24,36H,10-13,15,34H2,1-2H3,(H2,35,37)(H,38,40)/b7-5+/t23-,24+	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	570	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Bioresearch Center Curated by ChEMBL					Assay Description Inhibition of Tie2				Bioorg Med Chem Lett 17: 1167-71 (2007) Article DOI: 10.1016/j.bmcl.2006.12.035 BindingDB Entry DOI: 10.7270/Q24Q7TN6
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50202753 (CHEMBL232927 | N-(4-(7-(3-acetamidoprop-1-enyl)-4-...) Show SMILES COc1cc(ccc1NC(=O)c1cc2ccccc2n1C)-c1csc2c(\C=C\CNC(C)=O)cnc(N)c12 Show InChI InChI=1S/C29H27N5O3S/c1-17(35)31-12-6-8-20-15-32-28(30)26-21(16-38-27(20)26)18-10-11-22(25(14-18)37-3)33-29(36)24-13-19-7-4-5-9-23(19)34(24)2/h4-11,13-16H,12H2,1-3H3,(H2,30,32)(H,31,35)(H,33,36)/b8-6+	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	720	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Bioresearch Center Curated by ChEMBL					Assay Description Inhibition of Lck				Bioorg Med Chem Lett 17: 1167-71 (2007) Article DOI: 10.1016/j.bmcl.2006.12.035 BindingDB Entry DOI: 10.7270/Q24Q7TN6
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50202740 (CHEMBL232126 | trans-N-(4-(4-amino-7-(3-hydroxypro...) Show SMILES COc1cc(ccc1NC(=O)c1cc2ccccc2n1C)-c1csc2c(\C=C\CO)cnc(N)c12 Show InChI InChI=1S/C27H24N4O3S/c1-31-21-8-4-3-6-17(21)12-22(31)27(33)30-20-10-9-16(13-23(20)34-2)19-15-35-25-18(7-5-11-32)14-29-26(28)24(19)25/h3-10,12-15,32H,11H2,1-2H3,(H2,28,29)(H,30,33)/b7-5+	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	770	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Bioresearch Center Curated by ChEMBL					Assay Description Inhibition of Lck				Bioorg Med Chem Lett 17: 1167-71 (2007) Article DOI: 10.1016/j.bmcl.2006.12.035 BindingDB Entry DOI: 10.7270/Q24Q7TN6
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lyn (Homo sapiens (Human))	BDBM50202734 (CHEMBL232542 | N-(4-(4-amino-7-(3-(diethylamino)pr...) Show SMILES CCN(CC)C\C=C\c1cnc(N)c2c(csc12)-c1ccc(NC(=O)c2cc3ccccc3n2C)c(OC)c1 Show InChI InChI=1S/C31H33N5O2S/c1-5-36(6-2)15-9-11-22-18-33-30(32)28-23(19-39-29(22)28)20-13-14-24(27(17-20)38-4)34-31(37)26-16-21-10-7-8-12-25(21)35(26)3/h7-14,16-19H,5-6,15H2,1-4H3,(H2,32,33)(H,34,37)/b11-9+	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	1.18E+3	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Bioresearch Center Curated by ChEMBL					Assay Description Inhibition of Lyn				Bioorg Med Chem Lett 17: 1167-71 (2007) Article DOI: 10.1016/j.bmcl.2006.12.035 BindingDB Entry DOI: 10.7270/Q24Q7TN6
					More data for this Ligand-Target Pair
Tyrosine-protein kinase HCK (Homo sapiens (Human))	BDBM50202757 (CHEMBL396359 | N-(4-(4-amino-7-(3-oxo-3-(piperidin...) Show SMILES COc1cc(ccc1NC(=O)c1cc2ccccc2n1C)-c1csc2C(CN=C(N)c12)C=CC(=O)NC1CCNCC1 |w:31.35,t:30| Show InChI InChI=1S/C32H34N6O3S/c1-38-25-6-4-3-5-20(25)15-26(38)32(40)37-24-9-7-19(16-27(24)41-2)23-18-42-30-21(17-35-31(33)29(23)30)8-10-28(39)36-22-11-13-34-14-12-22/h3-10,15-16,18,21-22,34H,11-14,17H2,1-2H3,(H2,33,35)(H,36,39)(H,37,40)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.29E+3	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Bioresearch Center Curated by ChEMBL					Assay Description Inhibition of Hck				Bioorg Med Chem Lett 17: 1167-71 (2007) Article DOI: 10.1016/j.bmcl.2006.12.035 BindingDB Entry DOI: 10.7270/Q24Q7TN6
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50202748 (CHEMBL232731 | N-(4-(4-amino-7-(3-(methylsulfonami...) Show SMILES COc1cc(ccc1NC(=O)c1cc2ccccc2n1C)-c1csc2c(\C=C\CNS(C)(=O)=O)cnc(N)c12 Show InChI InChI=1S/C28H27N5O4S2/c1-33-22-9-5-4-7-18(22)13-23(33)28(34)32-21-11-10-17(14-24(21)37-2)20-16-38-26-19(15-30-27(29)25(20)26)8-6-12-31-39(3,35)36/h4-11,13-16,31H,12H2,1-3H3,(H2,29,30)(H,32,34)/b8-6+	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.37E+3	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Bioresearch Center Curated by ChEMBL					Assay Description Inhibition of Lck				Bioorg Med Chem Lett 17: 1167-71 (2007) Article DOI: 10.1016/j.bmcl.2006.12.035 BindingDB Entry DOI: 10.7270/Q24Q7TN6
					More data for this Ligand-Target Pair
Tyrosine-protein kinase HCK (Homo sapiens (Human))	BDBM50202744 (4-amino-3-(3-methoxy-4-(1-methyl-1H-indole-2-carbo...) Show SMILES COc1cc(ccc1NC(=O)c1cc2ccccc2n1C)-c1csc2c(cnc(N)c12)C(N)=O Show InChI InChI=1S/C25H21N5O3S/c1-30-18-6-4-3-5-14(18)9-19(30)25(32)29-17-8-7-13(10-20(17)33-2)16-12-34-22-15(24(27)31)11-28-23(26)21(16)22/h3-12H,1-2H3,(H2,26,28)(H2,27,31)(H,29,32)	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	1.41E+3	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Bioresearch Center Curated by ChEMBL					Assay Description Inhibition of Hck				Bioorg Med Chem Lett 17: 1167-71 (2007) Article DOI: 10.1016/j.bmcl.2006.12.035 BindingDB Entry DOI: 10.7270/Q24Q7TN6
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50202746 (CHEMBL395663 | N-(4-(4-amino-7-(3-(4-methyl-3-oxop...) Show SMILES COc1cc(ccc1NC(=O)c1cc2ccccc2n1C)-c1csc2c(C=CCN3CCN(C)C(=O)C3)cnc(N)c12 |w:26.28| Show InChI InChI=1S/C32H32N6O3S/c1-36-13-14-38(18-28(36)39)12-6-8-22-17-34-31(33)29-23(19-42-30(22)29)20-10-11-24(27(16-20)41-3)35-32(40)26-15-21-7-4-5-9-25(21)37(26)2/h4-11,15-17,19H,12-14,18H2,1-3H3,(H2,33,34)(H,35,40)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.52E+3	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Bioresearch Center Curated by ChEMBL					Assay Description Inhibition of Lck				Bioorg Med Chem Lett 17: 1167-71 (2007) Article DOI: 10.1016/j.bmcl.2006.12.035 BindingDB Entry DOI: 10.7270/Q24Q7TN6
					More data for this Ligand-Target Pair
Angiopoietin-1 receptor (Homo sapiens (Human))	BDBM50202737 (CHEMBL395665 | N-(4-(4-amino-7-(3-((1r,4r)-4-amino...) Show SMILES COc1cc(ccc1NC(=O)c1cc2ccccc2n1C)-c1csc2c(\C=C\CN[C@H]3CC[C@H](N)CC3)cnc(N)c12 |wU:30.32,wD:33.36,(5.61,-23.77,;4.15,-23.29,;3.01,-24.32,;1.54,-23.84,;.4,-24.87,;.73,-26.38,;2.18,-26.85,;3.33,-25.82,;4.78,-26.3,;5.1,-27.8,;3.96,-28.84,;6.57,-28.28,;7.04,-29.76,;8.59,-29.75,;9.62,-30.9,;11.13,-30.57,;11.61,-29.11,;10.57,-27.96,;9.07,-28.28,;7.83,-27.37,;7.83,-25.83,;-1.07,-24.39,;-2.31,-25.31,;-3.56,-24.4,;-3.08,-22.94,;-3.85,-21.62,;-5.39,-21.62,;-6.16,-20.29,;-7.7,-20.3,;-8.47,-18.96,;-7.71,-17.63,;-8.47,-16.3,;-7.7,-14.97,;-6.16,-14.97,;-5.39,-13.64,;-5.4,-16.3,;-6.16,-17.63,;-3.09,-20.3,;-1.55,-20.29,;-.79,-21.62,;.75,-21.62,;-1.55,-22.94,)| Show InChI InChI=1S/C33H36N6O2S/c1-39-27-8-4-3-6-21(27)16-28(39)33(40)38-26-14-9-20(17-29(26)41-2)25-19-42-31-22(18-37-32(35)30(25)31)7-5-15-36-24-12-10-23(34)11-13-24/h3-9,14,16-19,23-24,36H,10-13,15,34H2,1-2H3,(H2,35,37)(H,38,40)/b7-5+/t23-,24-	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.90E+3	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Bioresearch Center Curated by ChEMBL					Assay Description Inhibition of Tie2				Bioorg Med Chem Lett 17: 1167-71 (2007) Article DOI: 10.1016/j.bmcl.2006.12.035 BindingDB Entry DOI: 10.7270/Q24Q7TN6
					More data for this Ligand-Target Pair
Tyrosine-protein kinase HCK (Homo sapiens (Human))	BDBM50202733 (4-amino-N-(2-(dimethylamino)ethyl)-3-(3-methoxy-4-...) Show SMILES COc1cc(ccc1NC(=O)c1cc2ccccc2n1C)-c1csc2c(cnc(N)c12)C(=O)NCCN(C)C Show InChI InChI=1S/C29H30N6O3S/c1-34(2)12-11-31-28(36)19-15-32-27(30)25-20(16-39-26(19)25)17-9-10-21(24(14-17)38-4)33-29(37)23-13-18-7-5-6-8-22(18)35(23)3/h5-10,13-16H,11-12H2,1-4H3,(H2,30,32)(H,31,36)(H,33,37)	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	1.97E+3	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Bioresearch Center Curated by ChEMBL					Assay Description Inhibition of Hck				Bioorg Med Chem Lett 17: 1167-71 (2007) Article DOI: 10.1016/j.bmcl.2006.12.035 BindingDB Entry DOI: 10.7270/Q24Q7TN6
					More data for this Ligand-Target Pair
Tyrosine-protein kinase HCK (Homo sapiens (Human))	BDBM50202736 (CHEMBL231930 | trans-N-(4-(4-amino-7-(3-amino-3-ox...) Show SMILES COc1cc(ccc1NC(=O)c1cc2ccccc2n1C)-c1csc2c(\C=C\C(N)=O)cnc(N)c12 Show InChI InChI=1S/C27H23N5O3S/c1-32-20-6-4-3-5-16(20)11-21(32)27(34)31-19-9-7-15(12-22(19)35-2)18-14-36-25-17(8-10-23(28)33)13-30-26(29)24(18)25/h3-14H,1-2H3,(H2,28,33)(H2,29,30)(H,31,34)/b10-8+	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	2.26E+3	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Bioresearch Center Curated by ChEMBL					Assay Description Inhibition of Hck				Bioorg Med Chem Lett 17: 1167-71 (2007) Article DOI: 10.1016/j.bmcl.2006.12.035 BindingDB Entry DOI: 10.7270/Q24Q7TN6
					More data for this Ligand-Target Pair
Tyrosine-protein kinase HCK (Homo sapiens (Human))	BDBM50202740 (CHEMBL232126 | trans-N-(4-(4-amino-7-(3-hydroxypro...) Show SMILES COc1cc(ccc1NC(=O)c1cc2ccccc2n1C)-c1csc2c(\C=C\CO)cnc(N)c12 Show InChI InChI=1S/C27H24N4O3S/c1-31-21-8-4-3-6-17(21)12-22(31)27(33)30-20-10-9-16(13-23(20)34-2)19-15-35-25-18(7-5-11-32)14-29-26(28)24(19)25/h3-10,12-15,32H,11H2,1-2H3,(H2,28,29)(H,30,33)/b7-5+	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	2.36E+3	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Bioresearch Center Curated by ChEMBL					Assay Description Inhibition of Hck				Bioorg Med Chem Lett 17: 1167-71 (2007) Article DOI: 10.1016/j.bmcl.2006.12.035 BindingDB Entry DOI: 10.7270/Q24Q7TN6
					More data for this Ligand-Target Pair
Tyrosine-protein kinase HCK (Homo sapiens (Human))	BDBM50202753 (CHEMBL232927 | N-(4-(7-(3-acetamidoprop-1-enyl)-4-...) Show SMILES COc1cc(ccc1NC(=O)c1cc2ccccc2n1C)-c1csc2c(\C=C\CNC(C)=O)cnc(N)c12 Show InChI InChI=1S/C29H27N5O3S/c1-17(35)31-12-6-8-20-15-32-28(30)26-21(16-38-27(20)26)18-10-11-22(25(14-18)37-3)33-29(36)24-13-19-7-4-5-9-23(19)34(24)2/h4-11,13-16H,12H2,1-3H3,(H2,30,32)(H,31,35)(H,33,36)/b8-6+	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	2.36E+3	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Bioresearch Center Curated by ChEMBL					Assay Description Inhibition of Hck				Bioorg Med Chem Lett 17: 1167-71 (2007) Article DOI: 10.1016/j.bmcl.2006.12.035 BindingDB Entry DOI: 10.7270/Q24Q7TN6
					More data for this Ligand-Target Pair
Tyrosine-protein kinase HCK (Homo sapiens (Human))	BDBM50202745 (4-amino-3-(3-methoxy-4-(1-methyl-1H-indole-2-carbo...) Show SMILES COc1cc(ccc1NC(=O)c1cc2ccccc2n1C)-c1csc2c(cnc(N)c12)C(=O)NCCN1CCCC1 Show InChI InChI=1S/C31H32N6O3S/c1-36-24-8-4-3-7-20(24)15-25(36)31(39)35-23-10-9-19(16-26(23)40-2)22-18-41-28-21(17-34-29(32)27(22)28)30(38)33-11-14-37-12-5-6-13-37/h3-4,7-10,15-18H,5-6,11-14H2,1-2H3,(H2,32,34)(H,33,38)(H,35,39)	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	2.55E+3	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Bioresearch Center Curated by ChEMBL					Assay Description Inhibition of Hck				Bioorg Med Chem Lett 17: 1167-71 (2007) Article DOI: 10.1016/j.bmcl.2006.12.035 BindingDB Entry DOI: 10.7270/Q24Q7TN6
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50202756 (CHEMBL233540 | N-(4-(4-amino-7-(3-(4-phenylpiperaz...) Show SMILES COc1cc(ccc1NC(=O)c1cc2ccccc2n1C)-c1csc2c(\C=C\CN3CCN(CC3)c3ccccc3)cnc(N)c12 Show InChI InChI=1S/C37H36N6O2S/c1-41-31-13-7-6-9-26(31)21-32(41)37(44)40-30-15-14-25(22-33(30)45-2)29-24-46-35-27(23-39-36(38)34(29)35)10-8-16-42-17-19-43(20-18-42)28-11-4-3-5-12-28/h3-15,21-24H,16-20H2,1-2H3,(H2,38,39)(H,40,44)/b10-8+	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.95E+3	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Bioresearch Center Curated by ChEMBL					Assay Description Inhibition of Lck				Bioorg Med Chem Lett 17: 1167-71 (2007) Article DOI: 10.1016/j.bmcl.2006.12.035 BindingDB Entry DOI: 10.7270/Q24Q7TN6
					More data for this Ligand-Target Pair
Angiopoietin-1 receptor (Homo sapiens (Human))	BDBM50202739 (CHEMBL395664 | N-(4-(4-amino-7-(3-(piperidin-4-yla...) Show SMILES COc1cc(ccc1NC(=O)c1cc2ccccc2n1C)-c1csc2c(\C=C\CNC3CCNCC3)cnc(N)c12 Show InChI InChI=1S/C32H34N6O2S/c1-38-26-8-4-3-6-21(26)16-27(38)32(39)37-25-10-9-20(17-28(25)40-2)24-19-41-30-22(18-36-31(33)29(24)30)7-5-13-35-23-11-14-34-15-12-23/h3-10,16-19,23,34-35H,11-15H2,1-2H3,(H2,33,36)(H,37,39)/b7-5+	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.70E+3	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Bioresearch Center Curated by ChEMBL					Assay Description Inhibition of Tie2				Bioorg Med Chem Lett 17: 1167-71 (2007) Article DOI: 10.1016/j.bmcl.2006.12.035 BindingDB Entry DOI: 10.7270/Q24Q7TN6
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lyn (Homo sapiens (Human))	BDBM50202739 (CHEMBL395664 | N-(4-(4-amino-7-(3-(piperidin-4-yla...) Show SMILES COc1cc(ccc1NC(=O)c1cc2ccccc2n1C)-c1csc2c(\C=C\CNC3CCNCC3)cnc(N)c12 Show InChI InChI=1S/C32H34N6O2S/c1-38-26-8-4-3-6-21(26)16-27(38)32(39)37-25-10-9-20(17-28(25)40-2)24-19-41-30-22(18-36-31(33)29(24)30)7-5-13-35-23-11-14-34-15-12-23/h3-10,16-19,23,34-35H,11-15H2,1-2H3,(H2,33,36)(H,37,39)/b7-5+	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	3.70E+3	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Bioresearch Center Curated by ChEMBL					Assay Description Inhibition of Lyn				Bioorg Med Chem Lett 17: 1167-71 (2007) Article DOI: 10.1016/j.bmcl.2006.12.035 BindingDB Entry DOI: 10.7270/Q24Q7TN6
					More data for this Ligand-Target Pair
Tyrosine-protein kinase HCK (Homo sapiens (Human))	BDBM50202748 (CHEMBL232731 | N-(4-(4-amino-7-(3-(methylsulfonami...) Show SMILES COc1cc(ccc1NC(=O)c1cc2ccccc2n1C)-c1csc2c(\C=C\CNS(C)(=O)=O)cnc(N)c12 Show InChI InChI=1S/C28H27N5O4S2/c1-33-22-9-5-4-7-18(22)13-23(33)28(34)32-21-11-10-17(14-24(21)37-2)20-16-38-26-19(15-30-27(29)25(20)26)8-6-12-31-39(3,35)36/h4-11,13-16,31H,12H2,1-3H3,(H2,29,30)(H,32,34)/b8-6+	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	4.30E+3	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Bioresearch Center Curated by ChEMBL					Assay Description Inhibition of Hck				Bioorg Med Chem Lett 17: 1167-71 (2007) Article DOI: 10.1016/j.bmcl.2006.12.035 BindingDB Entry DOI: 10.7270/Q24Q7TN6
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50202750 (CHEMBL391247 | cis-N-(4-(4-amino-7-(3-(diethylamin...) Show SMILES CCN(CC)C\C=C/c1cnc(N)c2c(csc12)-c1ccc(NC(=O)c2cc3ccccc3n2C)c(OC)c1 Show InChI InChI=1S/C31H33N5O2S/c1-5-36(6-2)15-9-11-22-18-33-30(32)28-23(19-39-29(22)28)20-13-14-24(27(17-20)38-4)34-31(37)26-16-21-10-7-8-12-25(21)35(26)3/h7-14,16-19H,5-6,15H2,1-4H3,(H2,32,33)(H,34,37)/b11-9-	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4.47E+3	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Bioresearch Center Curated by ChEMBL					Assay Description Inhibition of Lck				Bioorg Med Chem Lett 17: 1167-71 (2007) Article DOI: 10.1016/j.bmcl.2006.12.035 BindingDB Entry DOI: 10.7270/Q24Q7TN6
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50202755 (CHEMBL391044 | N-(4-(4-amino-7-(3-hydroxypropyl)th...) Show SMILES COc1cc(ccc1NC(=O)c1cc2ccccc2n1C)-c1csc2c(CCCO)cnc(N)c12 Show InChI InChI=1S/C27H26N4O3S/c1-31-21-8-4-3-6-17(21)12-22(31)27(33)30-20-10-9-16(13-23(20)34-2)19-15-35-25-18(7-5-11-32)14-29-26(28)24(19)25/h3-4,6,8-10,12-15,32H,5,7,11H2,1-2H3,(H2,28,29)(H,30,33)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4.81E+3	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Bioresearch Center Curated by ChEMBL					Assay Description Inhibition of Lck				Bioorg Med Chem Lett 17: 1167-71 (2007) Article DOI: 10.1016/j.bmcl.2006.12.035 BindingDB Entry DOI: 10.7270/Q24Q7TN6
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50202758 (CHEMBL391475 | N-(4-(4-aminothieno[3,2-c]pyridin-3...) Show SMILES COc1cc(ccc1NC(=O)c1cc2ccccc2n1C)-c1csc2ccnc(N)c12 Show InChI InChI=1S/C24H20N4O2S/c1-28-18-6-4-3-5-15(18)11-19(28)24(29)27-17-8-7-14(12-20(17)30-2)16-13-31-21-9-10-26-23(25)22(16)21/h3-13H,1-2H3,(H2,25,26)(H,27,29)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5.20E+3	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Bioresearch Center Curated by ChEMBL					Assay Description Inhibition of Lck				Bioorg Med Chem Lett 17: 1167-71 (2007) Article DOI: 10.1016/j.bmcl.2006.12.035 BindingDB Entry DOI: 10.7270/Q24Q7TN6
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lyn (Homo sapiens (Human))	BDBM50202741 (CHEMBL233958 | N-(4-(4-amino-7-(3-(4-hydroxypiperi...) Show SMILES COc1cc(ccc1NC(=O)c1cc2ccccc2n1C)-c1csc2c(\C=C\CN3CCC(O)CC3)cnc(N)c12 Show InChI InChI=1S/C32H33N5O3S/c1-36-26-8-4-3-6-21(26)16-27(36)32(39)35-25-10-9-20(17-28(25)40-2)24-19-41-30-22(18-34-31(33)29(24)30)7-5-13-37-14-11-23(38)12-15-37/h3-10,16-19,23,38H,11-15H2,1-2H3,(H2,33,34)(H,35,39)/b7-5+	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	5.30E+3	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Bioresearch Center Curated by ChEMBL					Assay Description Inhibition of Lyn				Bioorg Med Chem Lett 17: 1167-71 (2007) Article DOI: 10.1016/j.bmcl.2006.12.035 BindingDB Entry DOI: 10.7270/Q24Q7TN6
					More data for this Ligand-Target Pair
Tyrosine-protein kinase HCK (Homo sapiens (Human))	BDBM50202754 (CHEMBL395662 | N-(4-(4-amino-7-(3-(4-methylpiperaz...) Show SMILES COc1cc(ccc1NC(=O)c1cc2ccccc2n1C)-c1csc2c(\C=C\CN3CCN(C)CC3)cnc(N)c12 Show InChI InChI=1S/C32H34N6O2S/c1-36-13-15-38(16-14-36)12-6-8-23-19-34-31(33)29-24(20-41-30(23)29)21-10-11-25(28(18-21)40-3)35-32(39)27-17-22-7-4-5-9-26(22)37(27)2/h4-11,17-20H,12-16H2,1-3H3,(H2,33,34)(H,35,39)/b8-6+	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	5.97E+3	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Bioresearch Center Curated by ChEMBL					Assay Description Inhibition of Hck				Bioorg Med Chem Lett 17: 1167-71 (2007) Article DOI: 10.1016/j.bmcl.2006.12.035 BindingDB Entry DOI: 10.7270/Q24Q7TN6
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50202751 (1-(3-(4-amino-3-(3-methoxy-4-(1-methyl-1H-indole-2...) Show SMILES COc1cc(ccc1NC(=O)c1cc2ccccc2n1C)-c1csc2c(\C=C\CNC(=O)Nc3ccccc3)cnc(N)c12 Show InChI InChI=1S/C34H30N6O3S/c1-40-27-13-7-6-9-22(27)17-28(40)33(41)39-26-15-14-21(18-29(26)43-2)25-20-44-31-23(19-37-32(35)30(25)31)10-8-16-36-34(42)38-24-11-4-3-5-12-24/h3-15,17-20H,16H2,1-2H3,(H2,35,37)(H,39,41)(H2,36,38,42)/b10-8+	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	6.70E+3	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Bioresearch Center Curated by ChEMBL					Assay Description Inhibition of Lck				Bioorg Med Chem Lett 17: 1167-71 (2007) Article DOI: 10.1016/j.bmcl.2006.12.035 BindingDB Entry DOI: 10.7270/Q24Q7TN6
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50202752 (1-(4-amino-3-(3-methoxy-4-(1-methyl-1H-indole-2-ca...) Show SMILES COc1cc(ccc1NC(=O)c1cc2ccccc2n1C)-c1csc2c(NC(=O)NCCN3CCCC3)cnc(N)c12 Show InChI InChI=1S/C31H33N7O3S/c1-37-24-8-4-3-7-20(24)15-25(37)30(39)35-22-10-9-19(16-26(22)41-2)21-18-42-28-23(17-34-29(32)27(21)28)36-31(40)33-11-14-38-12-5-6-13-38/h3-4,7-10,15-18H,5-6,11-14H2,1-2H3,(H2,32,34)(H,35,39)(H2,33,36,40)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	6.85E+3	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Bioresearch Center Curated by ChEMBL					Assay Description Inhibition of Lck				Bioorg Med Chem Lett 17: 1167-71 (2007) Article DOI: 10.1016/j.bmcl.2006.12.035 BindingDB Entry DOI: 10.7270/Q24Q7TN6
					More data for this Ligand-Target Pair
Tyrosine-protein kinase HCK (Homo sapiens (Human))	BDBM50202738 (CHEMBL232127 | trans-N-(4-(4-amino-7-(3-aminoprop-...) Show SMILES COc1cc(ccc1NC(=O)c1cc2ccccc2n1C)-c1csc2c(\C=C\CN)cnc(N)c12 Show InChI InChI=1S/C27H25N5O2S/c1-32-21-8-4-3-6-17(21)12-22(32)27(33)31-20-10-9-16(13-23(20)34-2)19-15-35-25-18(7-5-11-28)14-30-26(29)24(19)25/h3-10,12-15H,11,28H2,1-2H3,(H2,29,30)(H,31,33)/b7-5+	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	8.80E+3	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Bioresearch Center Curated by ChEMBL					Assay Description Inhibition of Hck				Bioorg Med Chem Lett 17: 1167-71 (2007) Article DOI: 10.1016/j.bmcl.2006.12.035 BindingDB Entry DOI: 10.7270/Q24Q7TN6
					More data for this Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src (Homo sapiens (Human))	BDBM50202734 (CHEMBL232542 | N-(4-(4-amino-7-(3-(diethylamino)pr...) Show SMILES CCN(CC)C\C=C\c1cnc(N)c2c(csc12)-c1ccc(NC(=O)c2cc3ccccc3n2C)c(OC)c1 Show InChI InChI=1S/C31H33N5O2S/c1-5-36(6-2)15-9-11-22-18-33-30(32)28-23(19-39-29(22)28)20-13-14-24(27(17-20)38-4)34-31(37)26-16-21-10-7-8-12-25(21)35(26)3/h7-14,16-19H,5-6,15H2,1-4H3,(H2,32,33)(H,34,37)/b11-9+	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	9.05E+3	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Bioresearch Center Curated by ChEMBL					Assay Description Inhibition of Src				Bioorg Med Chem Lett 17: 1167-71 (2007) Article DOI: 10.1016/j.bmcl.2006.12.035 BindingDB Entry DOI: 10.7270/Q24Q7TN6
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50202743 (CHEMBL233965 | N-(4-(4,7-diaminothieno[3,2-c]pyrid...) Show SMILES COc1cc(ccc1NC(=O)c1cc2ccccc2n1C)-c1csc2c(N)cnc(N)c12 Show InChI InChI=1S/C24H21N5O2S/c1-29-18-6-4-3-5-14(18)9-19(29)24(30)28-17-8-7-13(10-20(17)31-2)15-12-32-22-16(25)11-27-23(26)21(15)22/h3-12H,25H2,1-2H3,(H2,26,27)(H,28,30)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	9.65E+3	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Bioresearch Center Curated by ChEMBL					Assay Description Inhibition of Lck				Bioorg Med Chem Lett 17: 1167-71 (2007) Article DOI: 10.1016/j.bmcl.2006.12.035 BindingDB Entry DOI: 10.7270/Q24Q7TN6
					More data for this Ligand-Target Pair
Tyrosine-protein kinase HCK (Homo sapiens (Human))	BDBM50202741 (CHEMBL233958 | N-(4-(4-amino-7-(3-(4-hydroxypiperi...) Show SMILES COc1cc(ccc1NC(=O)c1cc2ccccc2n1C)-c1csc2c(\C=C\CN3CCC(O)CC3)cnc(N)c12 Show InChI InChI=1S/C32H33N5O3S/c1-36-26-8-4-3-6-21(26)16-27(36)32(39)35-25-10-9-20(17-28(25)40-2)24-19-41-30-22(18-34-31(33)29(24)30)7-5-13-37-14-11-23(38)12-15-37/h3-10,16-19,23,38H,11-15H2,1-2H3,(H2,33,34)(H,35,39)/b7-5+	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	1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Bioresearch Center Curated by ChEMBL					Assay Description Inhibition of Hck				Bioorg Med Chem Lett 17: 1167-71 (2007) Article DOI: 10.1016/j.bmcl.2006.12.035 BindingDB Entry DOI: 10.7270/Q24Q7TN6
					More data for this Ligand-Target Pair
Angiopoietin-1 receptor (Homo sapiens (Human))	BDBM50202741 (CHEMBL233958 | N-(4-(4-amino-7-(3-(4-hydroxypiperi...) Show SMILES COc1cc(ccc1NC(=O)c1cc2ccccc2n1C)-c1csc2c(\C=C\CN3CCC(O)CC3)cnc(N)c12 Show InChI InChI=1S/C32H33N5O3S/c1-36-26-8-4-3-6-21(26)16-27(36)32(39)35-25-10-9-20(17-28(25)40-2)24-19-41-30-22(18-34-31(33)29(24)30)7-5-13-37-14-11-23(38)12-15-37/h3-10,16-19,23,38H,11-15H2,1-2H3,(H2,33,34)(H,35,39)/b7-5+	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.01E+4	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Bioresearch Center Curated by ChEMBL					Assay Description Inhibition of Tie2				Bioorg Med Chem Lett 17: 1167-71 (2007) Article DOI: 10.1016/j.bmcl.2006.12.035 BindingDB Entry DOI: 10.7270/Q24Q7TN6
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lyn (Homo sapiens (Human))	BDBM50202735 (CHEMBL395666 | N-(4-(4-amino-7-(3-((1s,4s)-4-amino...) Show SMILES COc1cc(ccc1NC(=O)c1cc2ccccc2n1C)-c1csc2c(\C=C\CN[C@@H]3CC[C@H](N)CC3)cnc(N)c12 |wU:30.32,33.36,(28.87,-24.7,;27.4,-24.22,;26.26,-25.25,;24.79,-24.77,;23.65,-25.8,;23.98,-27.31,;25.43,-27.78,;26.58,-26.75,;28.03,-27.23,;28.36,-28.73,;27.21,-29.77,;29.82,-29.21,;30.29,-30.69,;31.84,-30.68,;32.87,-31.82,;34.38,-31.5,;34.86,-30.04,;33.82,-28.89,;32.32,-29.21,;31.08,-28.3,;31.08,-26.76,;22.18,-25.32,;20.94,-26.24,;19.69,-25.33,;20.17,-23.87,;19.4,-22.55,;17.86,-22.55,;17.09,-21.22,;15.55,-21.23,;14.78,-19.89,;15.54,-18.56,;17.09,-18.56,;17.85,-17.23,;17.09,-15.9,;17.86,-14.57,;15.55,-15.9,;14.78,-17.23,;20.16,-21.22,;21.7,-21.22,;22.47,-22.55,;24.01,-22.55,;21.7,-23.87,)| Show InChI InChI=1S/C33H36N6O2S/c1-39-27-8-4-3-6-21(27)16-28(39)33(40)38-26-14-9-20(17-29(26)41-2)25-19-42-31-22(18-37-32(35)30(25)31)7-5-15-36-24-12-10-23(34)11-13-24/h3-9,14,16-19,23-24,36H,10-13,15,34H2,1-2H3,(H2,35,37)(H,38,40)/b7-5+/t23-,24+	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	1.29E+4	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Bioresearch Center Curated by ChEMBL					Assay Description Inhibition of Lyn				Bioorg Med Chem Lett 17: 1167-71 (2007) Article DOI: 10.1016/j.bmcl.2006.12.035 BindingDB Entry DOI: 10.7270/Q24Q7TN6
					More data for this Ligand-Target Pair
Tyrosine-protein kinase HCK (Homo sapiens (Human))	BDBM50202746 (CHEMBL395663 | N-(4-(4-amino-7-(3-(4-methyl-3-oxop...) Show SMILES COc1cc(ccc1NC(=O)c1cc2ccccc2n1C)-c1csc2c(C=CCN3CCN(C)C(=O)C3)cnc(N)c12 |w:26.28| Show InChI InChI=1S/C32H32N6O3S/c1-36-13-14-38(18-28(36)39)12-6-8-22-17-34-31(33)29-23(19-42-30(22)29)20-10-11-24(27(16-20)41-3)35-32(40)26-15-21-7-4-5-9-25(21)37(26)2/h4-11,15-17,19H,12-14,18H2,1-3H3,(H2,33,34)(H,35,40)	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	1.29E+4	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Bioresearch Center Curated by ChEMBL					Assay Description Inhibition of Hck				Bioorg Med Chem Lett 17: 1167-71 (2007) Article DOI: 10.1016/j.bmcl.2006.12.035 BindingDB Entry DOI: 10.7270/Q24Q7TN6
					More data for this Ligand-Target Pair
Tyrosine-protein kinase HCK (Homo sapiens (Human))	BDBM50202734 (CHEMBL232542 | N-(4-(4-amino-7-(3-(diethylamino)pr...) Show SMILES CCN(CC)C\C=C\c1cnc(N)c2c(csc12)-c1ccc(NC(=O)c2cc3ccccc3n2C)c(OC)c1 Show InChI InChI=1S/C31H33N5O2S/c1-5-36(6-2)15-9-11-22-18-33-30(32)28-23(19-39-29(22)28)20-13-14-24(27(17-20)38-4)34-31(37)26-16-21-10-7-8-12-25(21)35(26)3/h7-14,16-19H,5-6,15H2,1-4H3,(H2,32,33)(H,34,37)/b11-9+	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	1.36E+4	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Bioresearch Center Curated by ChEMBL					Assay Description Inhibition of Hck				Bioorg Med Chem Lett 17: 1167-71 (2007) Article DOI: 10.1016/j.bmcl.2006.12.035 BindingDB Entry DOI: 10.7270/Q24Q7TN6
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Fgr (Homo sapiens (Human))	BDBM50202734 (CHEMBL232542 | N-(4-(4-amino-7-(3-(diethylamino)pr...) Show SMILES CCN(CC)C\C=C\c1cnc(N)c2c(csc12)-c1ccc(NC(=O)c2cc3ccccc3n2C)c(OC)c1 Show InChI InChI=1S/C31H33N5O2S/c1-5-36(6-2)15-9-11-22-18-33-30(32)28-23(19-39-29(22)28)20-13-14-24(27(17-20)38-4)34-31(37)26-16-21-10-7-8-12-25(21)35(26)3/h7-14,16-19H,5-6,15H2,1-4H3,(H2,32,33)(H,34,37)/b11-9+	PDB KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.41E+4	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Bioresearch Center Curated by ChEMBL					Assay Description Inhibition of Fgr				Bioorg Med Chem Lett 17: 1167-71 (2007) Article DOI: 10.1016/j.bmcl.2006.12.035 BindingDB Entry DOI: 10.7270/Q24Q7TN6
					More data for this Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src (Homo sapiens (Human))	BDBM50202739 (CHEMBL395664 | N-(4-(4-amino-7-(3-(piperidin-4-yla...) Show SMILES COc1cc(ccc1NC(=O)c1cc2ccccc2n1C)-c1csc2c(\C=C\CNC3CCNCC3)cnc(N)c12 Show InChI InChI=1S/C32H34N6O2S/c1-38-26-8-4-3-6-21(26)16-27(38)32(39)37-25-10-9-20(17-28(25)40-2)24-19-41-30-22(18-36-31(33)29(24)30)7-5-13-35-23-11-14-34-15-12-23/h3-10,16-19,23,34-35H,11-15H2,1-2H3,(H2,33,36)(H,37,39)/b7-5+	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.44E+4	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Bioresearch Center Curated by ChEMBL					Assay Description Inhibition of Src				Bioorg Med Chem Lett 17: 1167-71 (2007) Article DOI: 10.1016/j.bmcl.2006.12.035 BindingDB Entry DOI: 10.7270/Q24Q7TN6
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50202749 (CHEMBL232335 | N-(4-(4-amino-7-(1-methylpiperazine...) Show SMILES COc1cc(ccc1NC(=O)c1cc2ccccc2n1C)-c1csc2c(cnc(N)c12)C(=O)N1CCN(C)CC1 Show InChI InChI=1S/C30H30N6O3S/c1-34-10-12-36(13-11-34)30(38)20-16-32-28(31)26-21(17-40-27(20)26)18-8-9-22(25(15-18)39-3)33-29(37)24-14-19-6-4-5-7-23(19)35(24)2/h4-9,14-17H,10-13H2,1-3H3,(H2,31,32)(H,33,37)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.76E+4	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Bioresearch Center Curated by ChEMBL					Assay Description Inhibition of Lck				Bioorg Med Chem Lett 17: 1167-71 (2007) Article DOI: 10.1016/j.bmcl.2006.12.035 BindingDB Entry DOI: 10.7270/Q24Q7TN6
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Fgr (Homo sapiens (Human))	BDBM50202737 (CHEMBL395665 | N-(4-(4-amino-7-(3-((1r,4r)-4-amino...) Show SMILES COc1cc(ccc1NC(=O)c1cc2ccccc2n1C)-c1csc2c(\C=C\CN[C@H]3CC[C@H](N)CC3)cnc(N)c12 |wU:30.32,wD:33.36,(5.61,-23.77,;4.15,-23.29,;3.01,-24.32,;1.54,-23.84,;.4,-24.87,;.73,-26.38,;2.18,-26.85,;3.33,-25.82,;4.78,-26.3,;5.1,-27.8,;3.96,-28.84,;6.57,-28.28,;7.04,-29.76,;8.59,-29.75,;9.62,-30.9,;11.13,-30.57,;11.61,-29.11,;10.57,-27.96,;9.07,-28.28,;7.83,-27.37,;7.83,-25.83,;-1.07,-24.39,;-2.31,-25.31,;-3.56,-24.4,;-3.08,-22.94,;-3.85,-21.62,;-5.39,-21.62,;-6.16,-20.29,;-7.7,-20.3,;-8.47,-18.96,;-7.71,-17.63,;-8.47,-16.3,;-7.7,-14.97,;-6.16,-14.97,;-5.39,-13.64,;-5.4,-16.3,;-6.16,-17.63,;-3.09,-20.3,;-1.55,-20.29,;-.79,-21.62,;.75,-21.62,;-1.55,-22.94,)| Show InChI InChI=1S/C33H36N6O2S/c1-39-27-8-4-3-6-21(27)16-28(39)33(40)38-26-14-9-20(17-29(26)41-2)25-19-42-31-22(18-37-32(35)30(25)31)7-5-15-36-24-12-10-23(34)11-13-24/h3-9,14,16-19,23-24,36H,10-13,15,34H2,1-2H3,(H2,35,37)(H,38,40)/b7-5+/t23-,24-	PDB KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.79E+4	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Bioresearch Center Curated by ChEMBL					Assay Description Inhibition of Fgr				Bioorg Med Chem Lett 17: 1167-71 (2007) Article DOI: 10.1016/j.bmcl.2006.12.035 BindingDB Entry DOI: 10.7270/Q24Q7TN6
					More data for this Ligand-Target Pair

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