Compile Data Set for Download or QSAR

Found 102 hits with Last Name = 'tometzki' and Initial = 'gb'   

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))	BDBM50092228 (4-Amino-5-(4-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrim...) Show SMILES Nc1ncnc2n(cc(-c3ccc(Oc4ccccc4)cc3)c12)C1CCCC1 Show InChI InChI=1S/C23H22N4O/c24-22-21-20(14-27(17-6-4-5-7-17)23(21)26-15-25-22)16-10-12-19(13-11-16)28-18-8-2-1-3-9-18/h1-3,8-15,17H,4-7H2,(H2,24,25,26)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE MMDB PC cid PC sid PDB UniChem Patents Similars	PubMed	n/a	n/a	<1	n/a	n/a	n/a	n/a	n/a	n/a
BASF Bioresearch Corporation Curated by ChEMBL					Assay Description Inhibition of p56 Lck tyrosine kinase (catalytic domain)				Bioorg Med Chem Lett 10: 2171-4 (2001) BindingDB Entry DOI: 10.7270/Q2DB813K
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50092249 (4-[4-(4-Amino-7-tert-butyl-7H-pyrrolo[2,3-d]pyrimi...) Show SMILES CC(C)(C)n1cc(-c2ccc(Oc3ccc(O)cc3)cc2)c2c(N)ncnc12 Show InChI InChI=1S/C22H22N4O2/c1-22(2,3)26-12-18(19-20(23)24-13-25-21(19)26)14-4-8-16(9-5-14)28-17-10-6-15(27)7-11-17/h4-13,27H,1-3H3,(H2,23,24,25)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	<1	n/a	n/a	n/a	n/a	n/a	n/a
BASF Bioresearch Corporation Curated by ChEMBL					Assay Description Inhibition of p56 Lck tyrosine kinase (catalytic domain)				Bioorg Med Chem Lett 10: 2171-4 (2001) BindingDB Entry DOI: 10.7270/Q2DB813K
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50092233 (7-Isopropyl-5-(4-phenoxy-phenyl)-7H-pyrrolo[2,3-d]...) Show SMILES CC(C)n1cc(-c2ccc(Oc3ccccc3)cc2)c2c(N)ncnc12 Show InChI InChI=1S/C21H20N4O/c1-14(2)25-12-18(19-20(22)23-13-24-21(19)25)15-8-10-17(11-9-15)26-16-6-4-3-5-7-16/h3-14H,1-2H3,(H2,22,23,24)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	<1	n/a	n/a	n/a	n/a	n/a	n/a
BASF Bioresearch Corporation Curated by ChEMBL					Assay Description Inhibition of p56 Lck tyrosine kinase (catalytic domain)				Bioorg Med Chem Lett 10: 2171-4 (2001) BindingDB Entry DOI: 10.7270/Q2DB813K
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50092241 (7-tert-Butyl-5-[4-(4-methoxy-phenoxy)-phenyl]-7H-p...) Show SMILES COc1ccc(Oc2ccc(cc2)-c2cn(c3ncnc(N)c23)C(C)(C)C)cc1 Show InChI InChI=1S/C23H24N4O2/c1-23(2,3)27-13-19(20-21(24)25-14-26-22(20)27)15-5-7-17(8-6-15)29-18-11-9-16(28-4)10-12-18/h5-14H,1-4H3,(H2,24,25,26)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	<1	n/a	n/a	n/a	n/a	n/a	n/a
BASF Bioresearch Corporation Curated by ChEMBL					Assay Description Inhibition of p56 Lck tyrosine kinase (catalytic domain)				Bioorg Med Chem Lett 10: 2171-4 (2001) BindingDB Entry DOI: 10.7270/Q2DB813K
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50092225 (7-tert-Butyl-5-(4-phenoxy-phenyl)-7H-pyrrolo[2,3-d...) Show SMILES CC(C)(C)n1cc(-c2ccc(Oc3ccccc3)cc2)c2c(N)ncnc12 Show InChI InChI=1S/C22H22N4O/c1-22(2,3)26-13-18(19-20(23)24-14-25-21(19)26)15-9-11-17(12-10-15)27-16-7-5-4-6-8-16/h4-14H,1-3H3,(H2,23,24,25)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	2	n/a	n/a	n/a	n/a	n/a	n/a
BASF Bioresearch Corporation Curated by ChEMBL					Assay Description Inhibitory activity against p56 Lck tyrosine kinase at a concentration of 5 uM ATP.				Bioorg Med Chem Lett 10: 2171-4 (2001) BindingDB Entry DOI: 10.7270/Q2DB813K
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50092228 (4-Amino-5-(4-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrim...) Show SMILES Nc1ncnc2n(cc(-c3ccc(Oc4ccccc4)cc3)c12)C1CCCC1 Show InChI InChI=1S/C23H22N4O/c24-22-21-20(14-27(17-6-4-5-7-17)23(21)26-15-25-22)16-10-12-19(13-11-16)28-18-8-2-1-3-9-18/h1-3,8-15,17H,4-7H2,(H2,24,25,26)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE MMDB PC cid PC sid PDB UniChem Patents Similars	PubMed	n/a	n/a	2	n/a	n/a	n/a	n/a	n/a	n/a
BASF Bioresearch Corporation Curated by ChEMBL					Assay Description Inhibition of p56 Lck tyrosine kinase (catalytic domain)				Bioorg Med Chem Lett 10: 2171-4 (2001) BindingDB Entry DOI: 10.7270/Q2DB813K
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50092243 (CHEMBL70034 | {4-[4-(4-Amino-7-isopropyl-7H-pyrrol...) Show SMILES CC(C)n1cc(-c2ccc(Oc3ccc(CO)cc3)cc2)c2c(N)ncnc12 Show InChI InChI=1S/C22H22N4O2/c1-14(2)26-11-19(20-21(23)24-13-25-22(20)26)16-5-9-18(10-6-16)28-17-7-3-15(12-27)4-8-17/h3-11,13-14,27H,12H2,1-2H3,(H2,23,24,25)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	<3	n/a	n/a	n/a	n/a	n/a	n/a
BASF Bioresearch Corporation Curated by ChEMBL					Assay Description Inhibitory activity against p56 Lck tyrosine kinase at a concentration of 5 uM ATP.				Bioorg Med Chem Lett 10: 2171-4 (2001) BindingDB Entry DOI: 10.7270/Q2DB813K
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50092236 (CHEMBL71541 | {2-[4-(4-Amino-7-isopropyl-7H-pyrrol...) Show SMILES CC(C)n1cc(-c2ccc(Oc3ccccc3CO)cc2)c2c(N)ncnc12 Show InChI InChI=1S/C22H22N4O2/c1-14(2)26-11-18(20-21(23)24-13-25-22(20)26)15-7-9-17(10-8-15)28-19-6-4-3-5-16(19)12-27/h3-11,13-14,27H,12H2,1-2H3,(H2,23,24,25)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	<3	n/a	n/a	n/a	n/a	n/a	n/a
BASF Bioresearch Corporation Curated by ChEMBL					Assay Description Inhibition of p56 Lck tyrosine kinase (catalytic domain)				Bioorg Med Chem Lett 10: 2171-4 (2001) BindingDB Entry DOI: 10.7270/Q2DB813K
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50092244 (5-[4-(4-Amino-phenoxy)-phenyl]-7-tert-butyl-7H-pyr...) Show SMILES CC(C)(C)n1cc(-c2ccc(Oc3ccc(N)cc3)cc2)c2c(N)ncnc12 Show InChI InChI=1S/C22H23N5O/c1-22(2,3)27-12-18(19-20(24)25-13-26-21(19)27)14-4-8-16(9-5-14)28-17-10-6-15(23)7-11-17/h4-13H,23H2,1-3H3,(H2,24,25,26)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	<3	n/a	n/a	n/a	n/a	n/a	n/a
BASF Bioresearch Corporation Curated by ChEMBL					Assay Description Inhibitory activity against p56 Lck tyrosine kinase at a concentration of 5 uM ATP.				Bioorg Med Chem Lett 10: 2171-4 (2001) BindingDB Entry DOI: 10.7270/Q2DB813K
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50092254 (7-Isopropyl-5-[4-(2-nitro-phenoxy)-phenyl]-7H-pyrr...) Show SMILES CC(C)n1cc(-c2ccc(Oc3ccccc3[N+]([O-])=O)cc2)c2c(N)ncnc12 Show InChI InChI=1S/C21H19N5O3/c1-13(2)25-11-16(19-20(22)23-12-24-21(19)25)14-7-9-15(10-8-14)29-18-6-4-3-5-17(18)26(27)28/h3-13H,1-2H3,(H2,22,23,24)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	<3	n/a	n/a	n/a	n/a	n/a	n/a
BASF Bioresearch Corporation Curated by ChEMBL					Assay Description Inhibition of p56 Lck tyrosine kinase (catalytic domain)				Bioorg Med Chem Lett 10: 2171-4 (2001) BindingDB Entry DOI: 10.7270/Q2DB813K
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50092240 (5-[4-(3-Amino-phenoxy)-phenyl]-7-tert-butyl-7H-pyr...) Show SMILES CC(C)(C)n1cc(-c2ccc(Oc3cccc(N)c3)cc2)c2c(N)ncnc12 Show InChI InChI=1S/C22H23N5O/c1-22(2,3)27-12-18(19-20(24)25-13-26-21(19)27)14-7-9-16(10-8-14)28-17-6-4-5-15(23)11-17/h4-13H,23H2,1-3H3,(H2,24,25,26)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	<3	n/a	n/a	n/a	n/a	n/a	n/a
BASF Bioresearch Corporation Curated by ChEMBL					Assay Description Inhibition of p56 Lck tyrosine kinase (catalytic domain)				Bioorg Med Chem Lett 10: 2171-4 (2001) BindingDB Entry DOI: 10.7270/Q2DB813K
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50092256 (2-[4-(4-Amino-7-isopropyl-7H-pyrrolo[2,3-d]pyrimid...) Show SMILES CC(C)n1cc(-c2ccc(Oc3ccccc3C#N)cc2)c2c(N)ncnc12 Show InChI InChI=1S/C22H19N5O/c1-14(2)27-12-18(20-21(24)25-13-26-22(20)27)15-7-9-17(10-8-15)28-19-6-4-3-5-16(19)11-23/h3-10,12-14H,1-2H3,(H2,24,25,26)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	<3	n/a	n/a	n/a	n/a	n/a	n/a
BASF Bioresearch Corporation Curated by ChEMBL					Assay Description Inhibitory activity against p56 Lck tyrosine kinase at a concentration of 5 uM ATP.				Bioorg Med Chem Lett 10: 2171-4 (2001) BindingDB Entry DOI: 10.7270/Q2DB813K
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50092235 (5-[4-(2-Amino-phenoxy)-phenyl]-7-isopropyl-7H-pyrr...) Show SMILES CC(C)n1cc(-c2ccc(Oc3ccccc3N)cc2)c2c(N)ncnc12 Show InChI InChI=1S/C21H21N5O/c1-13(2)26-11-16(19-20(23)24-12-25-21(19)26)14-7-9-15(10-8-14)27-18-6-4-3-5-17(18)22/h3-13H,22H2,1-2H3,(H2,23,24,25)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	5	n/a	n/a	n/a	n/a	n/a	n/a
BASF Bioresearch Corporation Curated by ChEMBL					Assay Description Inhibitory activity against p56 Lck tyrosine kinase at a concentration of 5 microM ATP.				Bioorg Med Chem Lett 10: 2171-4 (2001) BindingDB Entry DOI: 10.7270/Q2DB813K
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50092239 (7-Cyclopentyl-5-[4-(2-methoxy-phenoxy)-phenyl]-7H-...) Show SMILES COc1ccccc1Oc1ccc(cc1)-c1cn(C2CCCC2)c2ncnc(N)c12 Show InChI InChI=1S/C24H24N4O2/c1-29-20-8-4-5-9-21(20)30-18-12-10-16(11-13-18)19-14-28(17-6-2-3-7-17)24-22(19)23(25)26-15-27-24/h4-5,8-15,17H,2-3,6-7H2,1H3,(H2,25,26,27)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	6	n/a	n/a	n/a	n/a	n/a	n/a
BASF Bioresearch Corporation Curated by ChEMBL					Assay Description Inhibitory activity against p56 Lck tyrosine kinase at a concentration of 5 microM ATP.				Bioorg Med Chem Lett 10: 2171-4 (2001) BindingDB Entry DOI: 10.7270/Q2DB813K
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50092234 (2-[4-(4-Amino-7-cyclopentyl-7H-pyrrolo[2,3-d]pyrim...) Show SMILES Nc1ncnc2n(cc(-c3ccc(Oc4ccccc4O)cc3)c12)C1CCCC1 Show InChI InChI=1S/C23H22N4O2/c24-22-21-18(13-27(16-5-1-2-6-16)23(21)26-14-25-22)15-9-11-17(12-10-15)29-20-8-4-3-7-19(20)28/h3-4,7-14,16,28H,1-2,5-6H2,(H2,24,25,26)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	8	n/a	n/a	n/a	n/a	n/a	n/a
BASF Bioresearch Corporation Curated by ChEMBL					Assay Description Inhibitory activity against p56 Lck tyrosine kinase at a concentration of 5 microM ATP.				Bioorg Med Chem Lett 10: 2171-4 (2001) BindingDB Entry DOI: 10.7270/Q2DB813K
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50092233 (7-Isopropyl-5-(4-phenoxy-phenyl)-7H-pyrrolo[2,3-d]...) Show SMILES CC(C)n1cc(-c2ccc(Oc3ccccc3)cc2)c2c(N)ncnc12 Show InChI InChI=1S/C21H20N4O/c1-14(2)25-12-18(19-20(22)23-13-24-21(19)25)15-8-10-17(11-9-15)26-16-6-4-3-5-7-16/h3-14H,1-2H3,(H2,22,23,24)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	10	n/a	n/a	n/a	n/a	n/a	n/a
BASF Bioresearch Corporation Curated by ChEMBL					Assay Description Inhibitory activity against p56 Lck tyrosine kinase at a concentration of 5 microM ATP.				Bioorg Med Chem Lett 10: 2171-4 (2001) BindingDB Entry DOI: 10.7270/Q2DB813K
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50092252 (6-Chloro-7-cyclopentyl-5-(4-phenoxy-phenyl)-7H-pyr...) Show SMILES Nc1ncnc2n(C3CCCC3)c(Cl)c(-c3ccc(Oc4ccccc4)cc3)c12 Show InChI InChI=1S/C23H21ClN4O/c24-21-19(15-10-12-18(13-11-15)29-17-8-2-1-3-9-17)20-22(25)26-14-27-23(20)28(21)16-6-4-5-7-16/h1-3,8-14,16H,4-7H2,(H2,25,26,27)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	11	n/a	n/a	n/a	n/a	n/a	n/a
BASF Bioresearch Corporation Curated by ChEMBL					Assay Description Inhibitory activity against p56 Lck tyrosine kinase at a concentration of 5 microM ATP.				Bioorg Med Chem Lett 10: 2171-4 (2001) BindingDB Entry DOI: 10.7270/Q2DB813K
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50092225 (7-tert-Butyl-5-(4-phenoxy-phenyl)-7H-pyrrolo[2,3-d...) Show SMILES CC(C)(C)n1cc(-c2ccc(Oc3ccccc3)cc2)c2c(N)ncnc12 Show InChI InChI=1S/C22H22N4O/c1-22(2,3)26-13-18(19-20(23)24-14-25-21(19)26)15-9-11-17(12-10-15)27-16-7-5-4-6-8-16/h4-14H,1-3H3,(H2,23,24,25)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	14	n/a	n/a	n/a	n/a	n/a	n/a
BASF Bioresearch Corporation Curated by ChEMBL					Assay Description Inhibition of p56 Lck tyrosine kinase (catalytic domain)				Bioorg Med Chem Lett 10: 2171-4 (2001) BindingDB Entry DOI: 10.7270/Q2DB813K
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50092240 (5-[4-(3-Amino-phenoxy)-phenyl]-7-tert-butyl-7H-pyr...) Show SMILES CC(C)(C)n1cc(-c2ccc(Oc3cccc(N)c3)cc2)c2c(N)ncnc12 Show InChI InChI=1S/C22H23N5O/c1-22(2,3)27-12-18(19-20(24)25-13-26-21(19)27)14-7-9-16(10-8-14)28-17-6-4-5-15(23)11-17/h4-13H,23H2,1-3H3,(H2,24,25,26)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	15	n/a	n/a	n/a	n/a	n/a	n/a
BASF Bioresearch Corporation Curated by ChEMBL					Assay Description Inhibition of p56 Lck tyrosine kinase (catalytic domain)				Bioorg Med Chem Lett 10: 2171-4 (2001) BindingDB Entry DOI: 10.7270/Q2DB813K
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50092249 (4-[4-(4-Amino-7-tert-butyl-7H-pyrrolo[2,3-d]pyrimi...) Show SMILES CC(C)(C)n1cc(-c2ccc(Oc3ccc(O)cc3)cc2)c2c(N)ncnc12 Show InChI InChI=1S/C22H22N4O2/c1-22(2,3)26-12-18(19-20(23)24-13-25-21(19)26)14-4-8-16(9-5-14)28-17-10-6-15(27)7-11-17/h4-13,27H,1-3H3,(H2,23,24,25)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	17	n/a	n/a	n/a	n/a	n/a	n/a
BASF Bioresearch Corporation Curated by ChEMBL					Assay Description Inhibition of p56 Lck tyrosine kinase (catalytic domain)				Bioorg Med Chem Lett 10: 2171-4 (2001) BindingDB Entry DOI: 10.7270/Q2DB813K
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50092250 (CHEMBL302279 | [4-Amino-7-cyclopentyl-5-(4-phenoxy...) Show SMILES Nc1ncnc2n(C3CCCC3)c(CO)c(-c3ccc(Oc4ccccc4)cc3)c12 Show InChI InChI=1S/C24H24N4O2/c25-23-22-21(16-10-12-19(13-11-16)30-18-8-2-1-3-9-18)20(14-29)28(17-6-4-5-7-17)24(22)27-15-26-23/h1-3,8-13,15,17,29H,4-7,14H2,(H2,25,26,27)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	17	n/a	n/a	n/a	n/a	n/a	n/a
BASF Bioresearch Corporation Curated by ChEMBL					Assay Description Inhibitory activity against p56 Lck tyrosine kinase at a concentration of 5 microM ATP.				Bioorg Med Chem Lett 10: 2171-4 (2001) BindingDB Entry DOI: 10.7270/Q2DB813K
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50092244 (5-[4-(4-Amino-phenoxy)-phenyl]-7-tert-butyl-7H-pyr...) Show SMILES CC(C)(C)n1cc(-c2ccc(Oc3ccc(N)cc3)cc2)c2c(N)ncnc12 Show InChI InChI=1S/C22H23N5O/c1-22(2,3)27-12-18(19-20(24)25-13-26-21(19)27)14-4-8-16(9-5-14)28-17-10-6-15(23)7-11-17/h4-13H,23H2,1-3H3,(H2,24,25,26)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	19	n/a	n/a	n/a	n/a	n/a	n/a
BASF Bioresearch Corporation Curated by ChEMBL					Assay Description Inhibition of p56 Lck tyrosine kinase (catalytic domain)				Bioorg Med Chem Lett 10: 2171-4 (2001) BindingDB Entry DOI: 10.7270/Q2DB813K
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50092239 (7-Cyclopentyl-5-[4-(2-methoxy-phenoxy)-phenyl]-7H-...) Show SMILES COc1ccccc1Oc1ccc(cc1)-c1cn(C2CCCC2)c2ncnc(N)c12 Show InChI InChI=1S/C24H24N4O2/c1-29-20-8-4-5-9-21(20)30-18-12-10-16(11-13-18)19-14-28(17-6-2-3-7-17)24-22(19)23(25)26-15-27-24/h4-5,8-15,17H,2-3,6-7H2,1H3,(H2,25,26,27)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	20	n/a	n/a	n/a	n/a	n/a	n/a
BASF Bioresearch Corporation Curated by ChEMBL					Assay Description Inhibition of p56 Lck tyrosine kinase (catalytic domain)				Bioorg Med Chem Lett 10: 2171-4 (2001) BindingDB Entry DOI: 10.7270/Q2DB813K
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50092246 (4-Amino-7-cyclopentyl-5-(4-phenoxy-phenyl)-7H-pyrr...) Show SMILES Nc1ncnc2n(C3CCCC3)c(C(O)=O)c(-c3ccc(Oc4ccccc4)cc3)c12 Show InChI InChI=1S/C24H22N4O3/c25-22-20-19(15-10-12-18(13-11-15)31-17-8-2-1-3-9-17)21(24(29)30)28(16-6-4-5-7-16)23(20)27-14-26-22/h1-3,8-14,16H,4-7H2,(H,29,30)(H2,25,26,27)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	20	n/a	n/a	n/a	n/a	n/a	n/a
BASF Bioresearch Corporation Curated by ChEMBL					Assay Description Inhibitory activity against p56 Lck tyrosine kinase at a concentration of 5 microM ATP.				Bioorg Med Chem Lett 10: 2171-4 (2001) BindingDB Entry DOI: 10.7270/Q2DB813K
					More data for this Ligand-Target Pair
Vascular endothelial growth factor receptor 2 (Homo sapiens (Human))	BDBM50092243 (CHEMBL70034 | {4-[4-(4-Amino-7-isopropyl-7H-pyrrol...) Show SMILES CC(C)n1cc(-c2ccc(Oc3ccc(CO)cc3)cc2)c2c(N)ncnc12 Show InChI InChI=1S/C22H22N4O2/c1-14(2)26-11-19(20-21(23)24-13-25-22(20)26)16-5-9-18(10-6-16)28-17-7-3-15(12-27)4-8-17/h3-11,13-14,27H,12H2,1-2H3,(H2,23,24,25)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	29	n/a	n/a	n/a	n/a	n/a	n/a
BASF Bioresearch Corporation Curated by ChEMBL					Assay Description Inhibitory activity against vascular endothelial growth factor receptor 2 (VEGFR2) at a concentration of 5 microM ATP.				Bioorg Med Chem Lett 10: 2171-4 (2001) BindingDB Entry DOI: 10.7270/Q2DB813K
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50092245 (4-Amino-7-cyclopentyl-5-(4-phenoxy-phenyl)-7H-pyrr...) Show SMILES NC(=O)c1c(-c2ccc(Oc3ccccc3)cc2)c2c(N)ncnc2n1C1CCCC1 Show InChI InChI=1S/C24H23N5O2/c25-22-20-19(15-10-12-18(13-11-15)31-17-8-2-1-3-9-17)21(23(26)30)29(16-6-4-5-7-16)24(20)28-14-27-22/h1-3,8-14,16H,4-7H2,(H2,26,30)(H2,25,27,28)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	30	n/a	n/a	n/a	n/a	n/a	n/a
BASF Bioresearch Corporation Curated by ChEMBL					Assay Description Inhibitory activity against p56 Lck tyrosine kinase at a concentration of 5 microM ATP.				Bioorg Med Chem Lett 10: 2171-4 (2001) BindingDB Entry DOI: 10.7270/Q2DB813K
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50092237 (6-Bromo-7-cyclopentyl-5-(4-phenoxy-phenyl)-7H-pyrr...) Show SMILES Nc1ncnc2n(C3CCCC3)c(Br)c(-c3ccc(Oc4ccccc4)cc3)c12 Show InChI InChI=1S/C23H21BrN4O/c24-21-19(15-10-12-18(13-11-15)29-17-8-2-1-3-9-17)20-22(25)26-14-27-23(20)28(21)16-6-4-5-7-16/h1-3,8-14,16H,4-7H2,(H2,25,26,27)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	30	n/a	n/a	n/a	n/a	n/a	n/a
BASF Bioresearch Corporation Curated by ChEMBL					Assay Description Inhibitory activity against p56 Lck tyrosine kinase at a concentration of 5 microM ATP.				Bioorg Med Chem Lett 10: 2171-4 (2001) BindingDB Entry DOI: 10.7270/Q2DB813K
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50092254 (7-Isopropyl-5-[4-(2-nitro-phenoxy)-phenyl]-7H-pyrr...) Show SMILES CC(C)n1cc(-c2ccc(Oc3ccccc3[N+]([O-])=O)cc2)c2c(N)ncnc12 Show InChI InChI=1S/C21H19N5O3/c1-13(2)25-11-16(19-20(22)23-12-24-21(19)25)14-7-9-15(10-8-14)29-18-6-4-3-5-17(18)26(27)28/h3-13H,1-2H3,(H2,22,23,24)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	38	n/a	n/a	n/a	n/a	n/a	n/a
BASF Bioresearch Corporation Curated by ChEMBL					Assay Description Inhibition of p56 Lck tyrosine kinase (catalytic domain)				Bioorg Med Chem Lett 10: 2171-4 (2001) BindingDB Entry DOI: 10.7270/Q2DB813K
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50092255 (4-[4-(4-Amino-7-isopropyl-7H-pyrrolo[2,3-d]pyrimid...) Show SMILES CC(C)n1cc(-c2ccc(Oc3ccc(cc3)C#N)cc2)c2c(N)ncnc12 Show InChI InChI=1S/C22H19N5O/c1-14(2)27-12-19(20-21(24)25-13-26-22(20)27)16-5-9-18(10-6-16)28-17-7-3-15(11-23)4-8-17/h3-10,12-14H,1-2H3,(H2,24,25,26)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	40	n/a	n/a	n/a	n/a	n/a	n/a
BASF Bioresearch Corporation Curated by ChEMBL					Assay Description Inhibitory activity against p56 Lck tyrosine kinase at a concentration of 5 microM ATP.				Bioorg Med Chem Lett 10: 2171-4 (2001) BindingDB Entry DOI: 10.7270/Q2DB813K
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50092252 (6-Chloro-7-cyclopentyl-5-(4-phenoxy-phenyl)-7H-pyr...) Show SMILES Nc1ncnc2n(C3CCCC3)c(Cl)c(-c3ccc(Oc4ccccc4)cc3)c12 Show InChI InChI=1S/C23H21ClN4O/c24-21-19(15-10-12-18(13-11-15)29-17-8-2-1-3-9-17)20-22(25)26-14-27-23(20)28(21)16-6-4-5-7-16/h1-3,8-14,16H,4-7H2,(H2,25,26,27)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	60	n/a	n/a	n/a	n/a	n/a	n/a
BASF Bioresearch Corporation Curated by ChEMBL					Assay Description Inhibition of p56 Lck tyrosine kinase (catalytic domain)				Bioorg Med Chem Lett 10: 2171-4 (2001) BindingDB Entry DOI: 10.7270/Q2DB813K
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50092241 (7-tert-Butyl-5-[4-(4-methoxy-phenoxy)-phenyl]-7H-p...) Show SMILES COc1ccc(Oc2ccc(cc2)-c2cn(c3ncnc(N)c23)C(C)(C)C)cc1 Show InChI InChI=1S/C23H24N4O2/c1-23(2,3)27-13-19(20-21(24)25-14-26-22(20)27)15-5-7-17(8-6-15)29-18-11-9-16(28-4)10-12-18/h5-14H,1-4H3,(H2,24,25,26)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	70	n/a	n/a	n/a	n/a	n/a	n/a
BASF Bioresearch Corporation Curated by ChEMBL					Assay Description Inhibition of p56 Lck tyrosine kinase (catalytic domain)				Bioorg Med Chem Lett 10: 2171-4 (2001) BindingDB Entry DOI: 10.7270/Q2DB813K
					More data for this Ligand-Target Pair
Vascular endothelial growth factor receptor 2 (Homo sapiens (Human))	BDBM50092234 (2-[4-(4-Amino-7-cyclopentyl-7H-pyrrolo[2,3-d]pyrim...) Show SMILES Nc1ncnc2n(cc(-c3ccc(Oc4ccccc4O)cc3)c12)C1CCCC1 Show InChI InChI=1S/C23H22N4O2/c24-22-21-18(13-27(16-5-1-2-6-16)23(21)26-14-25-22)15-9-11-17(12-10-15)29-20-8-4-3-7-19(20)28/h3-4,7-14,16,28H,1-2,5-6H2,(H2,24,25,26)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	90	n/a	n/a	n/a	n/a	n/a	n/a
BASF Bioresearch Corporation Curated by ChEMBL					Assay Description Inhibitory activity against vascular endothelial growth factor receptor 2 (VEGFR2) at a concentration of 5 microM ATP.				Bioorg Med Chem Lett 10: 2171-4 (2001) BindingDB Entry DOI: 10.7270/Q2DB813K
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Fyn (Homo sapiens (Human))	BDBM50092228 (4-Amino-5-(4-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrim...) Show SMILES Nc1ncnc2n(cc(-c3ccc(Oc4ccccc4)cc3)c12)C1CCCC1 Show InChI InChI=1S/C23H22N4O/c24-22-21-20(14-27(17-6-4-5-7-17)23(21)26-15-25-22)16-10-12-19(13-11-16)28-18-8-2-1-3-9-18/h1-3,8-15,17H,4-7H2,(H2,24,25,26)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE MMDB PC cid PC sid PDB UniChem Patents Similars	PubMed	n/a	n/a	126	n/a	n/a	n/a	n/a	n/a	n/a
BASF Bioresearch Corporation Curated by ChEMBL					Assay Description Inhibition of Fyn protein kinase				Bioorg Med Chem Lett 10: 2171-4 (2001) BindingDB Entry DOI: 10.7270/Q2DB813K
					More data for this Ligand-Target Pair
Vascular endothelial growth factor receptor 2 (Homo sapiens (Human))	BDBM50092255 (4-[4-(4-Amino-7-isopropyl-7H-pyrrolo[2,3-d]pyrimid...) Show SMILES CC(C)n1cc(-c2ccc(Oc3ccc(cc3)C#N)cc2)c2c(N)ncnc12 Show InChI InChI=1S/C22H19N5O/c1-14(2)27-12-19(20-21(24)25-13-26-22(20)27)16-5-9-18(10-6-16)28-17-7-3-15(11-23)4-8-17/h3-10,12-14H,1-2H3,(H2,24,25,26)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	129	n/a	n/a	n/a	n/a	n/a	n/a
BASF Bioresearch Corporation Curated by ChEMBL					Assay Description Inhibitory activity against vascular endothelial growth factor receptor 2 (VEGFR2) at a concentration of 5 microM ATP.				Bioorg Med Chem Lett 10: 2171-4 (2001) BindingDB Entry DOI: 10.7270/Q2DB813K
					More data for this Ligand-Target Pair
Angiopoietin-1 receptor (Homo sapiens (Human))	BDBM50092251 (6-Aminomethyl-7-cyclopentyl-5-(4-phenoxy-phenyl)-7...) Show SMILES NCc1c(-c2ccc(Oc3ccccc3)cc2)c2c(N)ncnc2n1C1CCCC1 Show InChI InChI=1S/C24H25N5O/c25-14-20-21(16-10-12-19(13-11-16)30-18-8-2-1-3-9-18)22-23(26)27-15-28-24(22)29(20)17-6-4-5-7-17/h1-3,8-13,15,17H,4-7,14,25H2,(H2,26,27,28)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	130	n/a	n/a	n/a	n/a	n/a	n/a
BASF Bioresearch Corporation Curated by ChEMBL					Assay Description Inhibitory activity against tie-2 at a concentration of 5 microM ATP.				Bioorg Med Chem Lett 10: 2171-4 (2001) BindingDB Entry DOI: 10.7270/Q2DB813K
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50092257 (4-[4-(4-Amino-7-isopropyl-7H-pyrrolo[2,3-d]pyrimid...) Show SMILES CC(C)n1cc(-c2ccc(Oc3ccc(cc3)C(O)=O)cc2)c2c(N)ncnc12 Show InChI InChI=1S/C22H20N4O3/c1-13(2)26-11-18(19-20(23)24-12-25-21(19)26)14-3-7-16(8-4-14)29-17-9-5-15(6-10-17)22(27)28/h3-13H,1-2H3,(H,27,28)(H2,23,24,25)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	131	n/a	n/a	n/a	n/a	n/a	n/a
BASF Bioresearch Corporation Curated by ChEMBL					Assay Description Inhibitory activity against p56 Lck tyrosine kinase at a concentration of 5 microM ATP.				Bioorg Med Chem Lett 10: 2171-4 (2001) BindingDB Entry DOI: 10.7270/Q2DB813K
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50092251 (6-Aminomethyl-7-cyclopentyl-5-(4-phenoxy-phenyl)-7...) Show SMILES NCc1c(-c2ccc(Oc3ccccc3)cc2)c2c(N)ncnc2n1C1CCCC1 Show InChI InChI=1S/C24H25N5O/c25-14-20-21(16-10-12-19(13-11-16)30-18-8-2-1-3-9-18)22-23(26)27-15-28-24(22)29(20)17-6-4-5-7-17/h1-3,8-13,15,17H,4-7,14,25H2,(H2,26,27,28)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	144	n/a	n/a	n/a	n/a	n/a	n/a
BASF Bioresearch Corporation Curated by ChEMBL					Assay Description Inhibitory activity against p56 Lck tyrosine kinase at a concentration of 5 microM ATP.				Bioorg Med Chem Lett 10: 2171-4 (2001) BindingDB Entry DOI: 10.7270/Q2DB813K
					More data for this Ligand-Target Pair
Vascular endothelial growth factor receptor 2 (Homo sapiens (Human))	BDBM50092236 (CHEMBL71541 | {2-[4-(4-Amino-7-isopropyl-7H-pyrrol...) Show SMILES CC(C)n1cc(-c2ccc(Oc3ccccc3CO)cc2)c2c(N)ncnc12 Show InChI InChI=1S/C22H22N4O2/c1-14(2)26-11-18(20-21(23)24-13-25-22(20)26)15-7-9-17(10-8-15)28-19-6-4-3-5-16(19)12-27/h3-11,13-14,27H,12H2,1-2H3,(H2,23,24,25)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	144	n/a	n/a	n/a	n/a	n/a	n/a
BASF Bioresearch Corporation Curated by ChEMBL					Assay Description Inhibitory activity against vascular endothelial growth factor receptor 2 (VEGFR2) at a concentration of 5 microM ATP.				Bioorg Med Chem Lett 10: 2171-4 (2001) BindingDB Entry DOI: 10.7270/Q2DB813K
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50092235 (5-[4-(2-Amino-phenoxy)-phenyl]-7-isopropyl-7H-pyrr...) Show SMILES CC(C)n1cc(-c2ccc(Oc3ccccc3N)cc2)c2c(N)ncnc12 Show InChI InChI=1S/C21H21N5O/c1-13(2)26-11-16(19-20(23)24-12-25-21(19)26)14-7-9-15(10-8-14)27-18-6-4-3-5-17(18)22/h3-13H,22H2,1-2H3,(H2,23,24,25)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	150	n/a	n/a	n/a	n/a	n/a	n/a
BASF Bioresearch Corporation Curated by ChEMBL					Assay Description Inhibition of p56 Lck tyrosine kinase (catalytic domain)				Bioorg Med Chem Lett 10: 2171-4 (2001) BindingDB Entry DOI: 10.7270/Q2DB813K
					More data for this Ligand-Target Pair
Vascular endothelial growth factor receptor 2 (Homo sapiens (Human))	BDBM50092256 (2-[4-(4-Amino-7-isopropyl-7H-pyrrolo[2,3-d]pyrimid...) Show SMILES CC(C)n1cc(-c2ccc(Oc3ccccc3C#N)cc2)c2c(N)ncnc12 Show InChI InChI=1S/C22H19N5O/c1-14(2)27-12-18(20-21(24)25-13-26-22(20)27)15-7-9-17(10-8-15)28-19-6-4-3-5-16(19)11-23/h3-10,12-14H,1-2H3,(H2,24,25,26)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	161	n/a	n/a	n/a	n/a	n/a	n/a
BASF Bioresearch Corporation Curated by ChEMBL					Assay Description Inhibitory activity against vascular endothelial growth factor receptor 2 (VEGFR2) at a concentration of 5 microM ATP.				Bioorg Med Chem Lett 10: 2171-4 (2001) BindingDB Entry DOI: 10.7270/Q2DB813K
					More data for this Ligand-Target Pair
Angiopoietin-1 receptor (Homo sapiens (Human))	BDBM50092236 (CHEMBL71541 | {2-[4-(4-Amino-7-isopropyl-7H-pyrrol...) Show SMILES CC(C)n1cc(-c2ccc(Oc3ccccc3CO)cc2)c2c(N)ncnc12 Show InChI InChI=1S/C22H22N4O2/c1-14(2)26-11-18(20-21(23)24-13-25-22(20)26)15-7-9-17(10-8-15)28-19-6-4-3-5-16(19)12-27/h3-11,13-14,27H,12H2,1-2H3,(H2,23,24,25)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	162	n/a	n/a	n/a	n/a	n/a	n/a
BASF Bioresearch Corporation Curated by ChEMBL					Assay Description Inhibitory activity against tie-2 at a concentration of 5 microM ATP.				Bioorg Med Chem Lett 10: 2171-4 (2001) BindingDB Entry DOI: 10.7270/Q2DB813K
					More data for this Ligand-Target Pair
Angiopoietin-1 receptor (Homo sapiens (Human))	BDBM50092256 (2-[4-(4-Amino-7-isopropyl-7H-pyrrolo[2,3-d]pyrimid...) Show SMILES CC(C)n1cc(-c2ccc(Oc3ccccc3C#N)cc2)c2c(N)ncnc12 Show InChI InChI=1S/C22H19N5O/c1-14(2)27-12-18(20-21(24)25-13-26-22(20)27)15-7-9-17(10-8-15)28-19-6-4-3-5-16(19)11-23/h3-10,12-14H,1-2H3,(H2,24,25,26)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	239	n/a	n/a	n/a	n/a	n/a	n/a
BASF Bioresearch Corporation Curated by ChEMBL					Assay Description Inhibitory activity against tie-2 at a concentration of 5 microM ATP.				Bioorg Med Chem Lett 10: 2171-4 (2001) BindingDB Entry DOI: 10.7270/Q2DB813K
					More data for this Ligand-Target Pair
Angiopoietin-1 receptor (Homo sapiens (Human))	BDBM50092243 (CHEMBL70034 | {4-[4-(4-Amino-7-isopropyl-7H-pyrrol...) Show SMILES CC(C)n1cc(-c2ccc(Oc3ccc(CO)cc3)cc2)c2c(N)ncnc12 Show InChI InChI=1S/C22H22N4O2/c1-14(2)26-11-19(20-21(23)24-13-25-22(20)26)16-5-9-18(10-6-16)28-17-7-3-15(12-27)4-8-17/h3-11,13-14,27H,12H2,1-2H3,(H2,23,24,25)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	246	n/a	n/a	n/a	n/a	n/a	n/a
BASF Bioresearch Corporation Curated by ChEMBL					Assay Description Inhibitory activity against tie-2 at a concentration of 5 microM ATP.				Bioorg Med Chem Lett 10: 2171-4 (2001) BindingDB Entry DOI: 10.7270/Q2DB813K
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50092238 (7-Cyclopentyl-6-methyl-5-(4-phenoxy-phenyl)-7H-pyr...) Show SMILES Cc1c(-c2ccc(Oc3ccccc3)cc2)c2c(N)ncnc2n1C1CCCC1 Show InChI InChI=1S/C24H24N4O/c1-16-21(17-11-13-20(14-12-17)29-19-9-3-2-4-10-19)22-23(25)26-15-27-24(22)28(16)18-7-5-6-8-18/h2-4,9-15,18H,5-8H2,1H3,(H2,25,26,27)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	260	n/a	n/a	n/a	n/a	n/a	n/a
BASF Bioresearch Corporation Curated by ChEMBL					Assay Description Inhibitory activity against p56 Lck tyrosine kinase at a concentration of 5 microM ATP.				Bioorg Med Chem Lett 10: 2171-4 (2001) BindingDB Entry DOI: 10.7270/Q2DB813K
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50092258 (7-Cyclopentyl-6-methoxymethyl-5-(4-phenoxy-phenyl)...) Show SMILES COCc1c(-c2ccc(Oc3ccccc3)cc2)c2c(N)ncnc2n1C1CCCC1 Show InChI InChI=1S/C25H26N4O2/c1-30-15-21-22(17-11-13-20(14-12-17)31-19-9-3-2-4-10-19)23-24(26)27-16-28-25(23)29(21)18-7-5-6-8-18/h2-4,9-14,16,18H,5-8,15H2,1H3,(H2,26,27,28)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	310	n/a	n/a	n/a	n/a	n/a	n/a
BASF Bioresearch Corporation Curated by ChEMBL					Assay Description Inhibitory activity against p56 Lck tyrosine kinase at a concentration of 5 microM ATP.				Bioorg Med Chem Lett 10: 2171-4 (2001) BindingDB Entry DOI: 10.7270/Q2DB813K
					More data for this Ligand-Target Pair
Tyrosine-protein kinase Lck (Homo sapiens (Human))	BDBM50092234 (2-[4-(4-Amino-7-cyclopentyl-7H-pyrrolo[2,3-d]pyrim...) Show SMILES Nc1ncnc2n(cc(-c3ccc(Oc4ccccc4O)cc3)c12)C1CCCC1 Show InChI InChI=1S/C23H22N4O2/c24-22-21-18(13-27(16-5-1-2-6-16)23(21)26-14-25-22)15-9-11-17(12-10-15)29-20-8-4-3-7-19(20)28/h3-4,7-14,16,28H,1-2,5-6H2,(H2,24,25,26)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	330	n/a	n/a	n/a	n/a	n/a	n/a
BASF Bioresearch Corporation Curated by ChEMBL					Assay Description Inhibitory activity against p56 Lck tyrosine kinase at a concentration of 5 microM ATP.				Bioorg Med Chem Lett 10: 2171-4 (2001) BindingDB Entry DOI: 10.7270/Q2DB813K
					More data for this Ligand-Target Pair
Angiopoietin-1 receptor (Homo sapiens (Human))	BDBM50092250 (CHEMBL302279 | [4-Amino-7-cyclopentyl-5-(4-phenoxy...) Show SMILES Nc1ncnc2n(C3CCCC3)c(CO)c(-c3ccc(Oc4ccccc4)cc3)c12 Show InChI InChI=1S/C24H24N4O2/c25-23-22-21(16-10-12-19(13-11-16)30-18-8-2-1-3-9-18)20(14-29)28(17-6-4-5-7-17)24(22)27-15-26-23/h1-3,8-13,15,17,29H,4-7,14H2,(H2,25,26,27)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	360	n/a	n/a	n/a	n/a	n/a	n/a
BASF Bioresearch Corporation Curated by ChEMBL					Assay Description Inhibitory activity against tie-2 at a concentration of 5 microM ATP.				Bioorg Med Chem Lett 10: 2171-4 (2001) BindingDB Entry DOI: 10.7270/Q2DB813K
					More data for this Ligand-Target Pair
Vascular endothelial growth factor receptor 2 (Homo sapiens (Human))	BDBM50092240 (5-[4-(3-Amino-phenoxy)-phenyl]-7-tert-butyl-7H-pyr...) Show SMILES CC(C)(C)n1cc(-c2ccc(Oc3cccc(N)c3)cc2)c2c(N)ncnc12 Show InChI InChI=1S/C22H23N5O/c1-22(2,3)27-12-18(19-20(24)25-13-26-21(19)27)14-7-9-16(10-8-14)28-17-6-4-5-15(23)11-17/h4-13H,23H2,1-3H3,(H2,24,25,26)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	400	n/a	n/a	n/a	n/a	n/a	n/a
BASF Bioresearch Corporation Curated by ChEMBL					Assay Description Inhibitory activity against vascular endothelial growth factor receptor 2 (VEGFR2) at a concentration of 5 microM ATP.				Bioorg Med Chem Lett 10: 2171-4 (2001) BindingDB Entry DOI: 10.7270/Q2DB813K
					More data for this Ligand-Target Pair
Angiopoietin-1 receptor (Homo sapiens (Human))	BDBM50092235 (5-[4-(2-Amino-phenoxy)-phenyl]-7-isopropyl-7H-pyrr...) Show SMILES CC(C)n1cc(-c2ccc(Oc3ccccc3N)cc2)c2c(N)ncnc12 Show InChI InChI=1S/C21H21N5O/c1-13(2)26-11-16(19-20(23)24-12-25-21(19)26)14-7-9-15(10-8-14)27-18-6-4-3-5-17(18)22/h3-13H,22H2,1-2H3,(H2,23,24,25)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	400	n/a	n/a	n/a	n/a	n/a	n/a
BASF Bioresearch Corporation Curated by ChEMBL					Assay Description Inhibitory activity against tie-2 at a concentration of 5 microM ATP.				Bioorg Med Chem Lett 10: 2171-4 (2001) BindingDB Entry DOI: 10.7270/Q2DB813K
					More data for this Ligand-Target Pair
Angiopoietin-1 receptor (Homo sapiens (Human))	BDBM50092246 (4-Amino-7-cyclopentyl-5-(4-phenoxy-phenyl)-7H-pyrr...) Show SMILES Nc1ncnc2n(C3CCCC3)c(C(O)=O)c(-c3ccc(Oc4ccccc4)cc3)c12 Show InChI InChI=1S/C24H22N4O3/c25-22-20-19(15-10-12-18(13-11-15)31-17-8-2-1-3-9-17)21(24(29)30)28(16-6-4-5-7-16)23(20)27-14-26-22/h1-3,8-14,16H,4-7H2,(H,29,30)(H2,25,26,27)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	410	n/a	n/a	n/a	n/a	n/a	n/a
BASF Bioresearch Corporation Curated by ChEMBL					Assay Description Inhibitory activity against tie-2 at a concentration of 5 microM ATP.				Bioorg Med Chem Lett 10: 2171-4 (2001) BindingDB Entry DOI: 10.7270/Q2DB813K
					More data for this Ligand-Target Pair

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