Affinity Data by PubMed id=1995903

PubMed code 1995903

Found 49 hits of Enzyme Inhibition Constant Data
Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kJ/mole	IC50 nM	Kd nM	EC50/IC50 nM	k_off s^-1	k_on M^-1s^-1	pH	Temp °C
SRC (Homo sapiens (Human))	BDBM50011418 (2-(4-Amino-phenyl)-6-hydroxy-chromen-4-one \| 2-(4-...) Show SMILES Nc1ccc(cc1)-c1cc(=O)c2cc(O)ccc2o1 Show InChI	PDB Reactome pathway UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	1.20E+3	n/a	n/a	n/a	n/a	n/a	n/a
Purdue University Curated by ChEMBL					Assay Description Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.				J Med Chem 34: 798-806 (1991) Article DOI: 10.1021/jm00106a047 BindingDB Entry DOI: 10.7270/Q2CF9P3J
Purdue University Curated by ChEMBL					More data for this Ligand-Target Pair
SRC (Homo sapiens (Human))	BDBM50011429 (2-(4-Amino-phenyl)-5,7-dihydroxy-chromen-4-one \| 2...) Show SMILES Nc1ccc(cc1)-c1cc(=O)c2c(O)cc(O)cc2o1 Show InChI	PDB Reactome pathway UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	7.40E+3	n/a	n/a	n/a	n/a	n/a	n/a
Purdue University Curated by ChEMBL					Assay Description Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.				J Med Chem 34: 798-806 (1991) Article DOI: 10.1021/jm00106a047 BindingDB Entry DOI: 10.7270/Q2CF9P3J
Purdue University Curated by ChEMBL					More data for this Ligand-Target Pair
SRC (Homo sapiens (Human))	BDBM7460 (2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-4H-chrome...) Show SMILES Show InChI	PDB Reactome pathway UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar	Purchase CHEBI CHEMBL DrugBank KEGG MMDB PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	1.30E+4	n/a	n/a	n/a	n/a	n/a	n/a
Purdue University Curated by ChEMBL					Assay Description Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.				J Med Chem 34: 798-806 (1991) Article DOI: 10.1021/jm00106a047 BindingDB Entry DOI: 10.7270/Q2CF9P3J
Purdue University Curated by ChEMBL					More data for this Ligand-Target Pair
SRC (Homo sapiens (Human))	BDBM50011424 (2-(4-Hydroxy-3,5-dimethoxy-phenyl)-chromen-4-one \|...) Show SMILES COc1cc(cc(OC)c1O)-c1cc(=O)c2ccccc2o1 Show InChI	PDB Reactome pathway UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.60E+4	n/a	n/a	n/a	n/a	n/a	n/a
Purdue University Curated by ChEMBL					Assay Description Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.				J Med Chem 34: 798-806 (1991) Article DOI: 10.1021/jm00106a047 BindingDB Entry DOI: 10.7270/Q2CF9P3J
Purdue University Curated by ChEMBL					More data for this Ligand-Target Pair
SRC (Homo sapiens (Human))	BDBM50011438 (2-(4-Amino-phenyl)-7-hydroxy-chromen-4-one \| 2-(4-...) Show SMILES Nc1ccc(cc1)-c1cc(=O)c2ccc(O)cc2o1 Show InChI	PDB Reactome pathway UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.38E+5	n/a	n/a	n/a	n/a	n/a	n/a
Purdue University Curated by ChEMBL					Assay Description Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.				J Med Chem 34: 798-806 (1991) Article DOI: 10.1021/jm00106a047 BindingDB Entry DOI: 10.7270/Q2CF9P3J
Purdue University Curated by ChEMBL					More data for this Ligand-Target Pair
SRC (Homo sapiens (Human))	BDBM50011437 (2-(4-Amino-phenyl)-chromen-4-one \| 2-(4-aminopheny...) Show SMILES Nc1ccc(cc1)-c1cc(=O)c2ccccc2o1 Show InChI	PDB Reactome pathway UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.10E+5	n/a	n/a	n/a	n/a	n/a	n/a
Purdue University Curated by ChEMBL					Assay Description Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.				J Med Chem 34: 798-806 (1991) Article DOI: 10.1021/jm00106a047 BindingDB Entry DOI: 10.7270/Q2CF9P3J
Purdue University Curated by ChEMBL					More data for this Ligand-Target Pair
SRC (Homo sapiens (Human))	BDBM50011455 (2-(4-Hydroxy-phenyl)-4-oxo-4H-chromene-3-carboxyli...) Show SMILES COC(=O)c1c(oc2ccccc2c1=O)-c1ccc(O)cc1 Show InChI	PDB Reactome pathway UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4.39E+5	n/a	n/a	n/a	n/a	n/a	n/a
Purdue University Curated by ChEMBL					Assay Description Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.				J Med Chem 34: 798-806 (1991) Article DOI: 10.1021/jm00106a047 BindingDB Entry DOI: 10.7270/Q2CF9P3J
Purdue University Curated by ChEMBL					More data for this Ligand-Target Pair
SRC (Homo sapiens (Human))	BDBM50011446 (2-(4-Hydroxy-phenyl)-chromen-4-one \| 2-(4-hydroxyp...) Show SMILES Oc1ccc(cc1)-c1cc(=O)c2ccccc2o1 Show InChI	PDB Reactome pathway UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar	Purchase CHEMBL MMDB PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	5.04E+5	n/a	n/a	n/a	n/a	n/a	n/a
Purdue University Curated by ChEMBL					Assay Description Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.				J Med Chem 34: 798-806 (1991) Article DOI: 10.1021/jm00106a047 BindingDB Entry DOI: 10.7270/Q2CF9P3J
Purdue University Curated by ChEMBL					More data for this Ligand-Target Pair
SRC (Homo sapiens (Human))	BDBM50011416 (2-(4-Amino-phenyl)-4-oxo-4H-chromene-3-carboxylic ...) Show SMILES COC(=O)c1c(oc2ccccc2c1=O)-c1ccc(N)cc1 Show InChI	PDB Reactome pathway UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	8.10E+5	n/a	n/a	n/a	n/a	n/a	n/a
Purdue University Curated by ChEMBL					Assay Description Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.				J Med Chem 34: 798-806 (1991) Article DOI: 10.1021/jm00106a047 BindingDB Entry DOI: 10.7270/Q2CF9P3J
Purdue University Curated by ChEMBL					More data for this Ligand-Target Pair
SRC (Homo sapiens (Human))	BDBM50011422 (2-(4-Hydroxy-phenyl)-7-methoxy-4-oxo-4H-chromene-3...) Show SMILES Show InChI	PDB Reactome pathway UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.03E+6	n/a	n/a	n/a	n/a	n/a	n/a
Purdue University Curated by ChEMBL					Assay Description Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.				J Med Chem 34: 798-806 (1991) Article DOI: 10.1021/jm00106a047 BindingDB Entry DOI: 10.7270/Q2CF9P3J
Purdue University Curated by ChEMBL					More data for this Ligand-Target Pair
SRC (Homo sapiens (Human))	BDBM50011451 (3-(2-Hydroxy-4-methoxy-phenyl)-3-oxo-propionic aci...) Show SMILES COC(=O)CC(=O)c1ccc(OC)cc1O Show InChI	PDB Reactome pathway UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.16E+6	n/a	n/a	n/a	n/a	n/a	n/a
Purdue University Curated by ChEMBL					Assay Description Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.				J Med Chem 34: 798-806 (1991) Article DOI: 10.1021/jm00106a047 BindingDB Entry DOI: 10.7270/Q2CF9P3J
Purdue University Curated by ChEMBL					More data for this Ligand-Target Pair
SRC (Homo sapiens (Human))	BDBM50011458 (2-(4-Hydroxy-phenyl)-4-oxo-4H-chromene-3-carboxyli...) Show SMILES OC(=O)c1c(oc2ccccc2c1=O)-c1ccc(O)cc1 Show InChI	PDB Reactome pathway UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.60E+6	n/a	n/a	n/a	n/a	n/a	n/a
Purdue University Curated by ChEMBL					Assay Description Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.				J Med Chem 34: 798-806 (1991) Article DOI: 10.1021/jm00106a047 BindingDB Entry DOI: 10.7270/Q2CF9P3J
Purdue University Curated by ChEMBL					More data for this Ligand-Target Pair
SRC (Homo sapiens (Human))	BDBM50011419 (6-Methoxy-2-(4-nitro-phenyl)-4-oxo-4H-chromene-3-c...) Show SMILES Show InChI	PDB Reactome pathway UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>2.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Purdue University Curated by ChEMBL					Assay Description Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.				J Med Chem 34: 798-806 (1991) Article DOI: 10.1021/jm00106a047 BindingDB Entry DOI: 10.7270/Q2CF9P3J
Purdue University Curated by ChEMBL					More data for this Ligand-Target Pair
SRC (Homo sapiens (Human))	BDBM50011426 (2-(4-Hydroxy-phenyl)-7-methoxy-4-oxo-4H-chromene-3...) Show SMILES Show InChI	PDB Reactome pathway UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>2.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Purdue University Curated by ChEMBL					Assay Description Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.				J Med Chem 34: 798-806 (1991) Article DOI: 10.1021/jm00106a047 BindingDB Entry DOI: 10.7270/Q2CF9P3J
Purdue University Curated by ChEMBL					More data for this Ligand-Target Pair
SRC (Homo sapiens (Human))	BDBM50011427 (7-Hydroxy-2-(4-nitro-phenyl)-chromen-4-one \| 7-hyd...) Show SMILES Show InChI	PDB Reactome pathway UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>2.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Purdue University Curated by ChEMBL					Assay Description Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.				J Med Chem 34: 798-806 (1991) Article DOI: 10.1021/jm00106a047 BindingDB Entry DOI: 10.7270/Q2CF9P3J
Purdue University Curated by ChEMBL					More data for this Ligand-Target Pair
SRC (Homo sapiens (Human))	BDBM50011435 (3-(2-Hydroxy-5-methoxy-phenyl)-3-oxo-propionic aci...) Show SMILES COC(=O)CC(=O)c1cc(OC)ccc1O Show InChI	PDB Reactome pathway UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>2.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Purdue University Curated by ChEMBL					Assay Description Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.				J Med Chem 34: 798-806 (1991) Article DOI: 10.1021/jm00106a047 BindingDB Entry DOI: 10.7270/Q2CF9P3J
Purdue University Curated by ChEMBL					More data for this Ligand-Target Pair
SRC (Homo sapiens (Human))	BDBM50011441 (2-(4-Methoxy-phenyl)-4-oxo-4H-chromene-3-carboxyli...) Show SMILES COc1ccc(cc1)-c1oc2ccccc2c(=O)c1C(O)=O Show InChI	PDB Reactome pathway UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>2.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Purdue University Curated by ChEMBL					Assay Description Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.				J Med Chem 34: 798-806 (1991) Article DOI: 10.1021/jm00106a047 BindingDB Entry DOI: 10.7270/Q2CF9P3J
Purdue University Curated by ChEMBL					More data for this Ligand-Target Pair
SRC (Homo sapiens (Human))	BDBM50011448 (4-Oxo-2-[4-(3,4,5-trimethoxy-benzoylamino)-phenyl]...) Show SMILES Show InChI	PDB Reactome pathway UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>2.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Purdue University Curated by ChEMBL					Assay Description Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.				J Med Chem 34: 798-806 (1991) Article DOI: 10.1021/jm00106a047 BindingDB Entry DOI: 10.7270/Q2CF9P3J
Purdue University Curated by ChEMBL					More data for this Ligand-Target Pair
SRC (Homo sapiens (Human))	BDBM50011460 (2-(4-Acetylamino-phenyl)-7-methoxy-4-oxo-4H-chrome...) Show SMILES Show InChI	PDB Reactome pathway UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>2.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Purdue University Curated by ChEMBL					Assay Description Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.				J Med Chem 34: 798-806 (1991) Article DOI: 10.1021/jm00106a047 BindingDB Entry DOI: 10.7270/Q2CF9P3J
Purdue University Curated by ChEMBL					More data for this Ligand-Target Pair
SRC (Homo sapiens (Human))	BDBM50011425 (2-(3,4-Dimethoxy-phenyl)-4-oxo-4H-chromene-3-carbo...) Show SMILES Show InChI	PDB Reactome pathway UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>2.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Purdue University Curated by ChEMBL					Assay Description Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.				J Med Chem 34: 798-806 (1991) Article DOI: 10.1021/jm00106a047 BindingDB Entry DOI: 10.7270/Q2CF9P3J
Purdue University Curated by ChEMBL					More data for this Ligand-Target Pair
SRC (Homo sapiens (Human))	BDBM50011432 (2-(3,4-Dimethoxy-phenyl)-4-oxo-4H-chromene-3-carbo...) Show SMILES COc1ccc(cc1OC)-c1oc2ccccc2c(=O)c1C(O)=O Show InChI	PDB Reactome pathway UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>2.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Purdue University Curated by ChEMBL					Assay Description Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.				J Med Chem 34: 798-806 (1991) Article DOI: 10.1021/jm00106a047 BindingDB Entry DOI: 10.7270/Q2CF9P3J
Purdue University Curated by ChEMBL					More data for this Ligand-Target Pair
SRC (Homo sapiens (Human))	BDBM50011434 (2-(4-Bromo-phenyl)-4-oxo-4H-chromene-3-carboxylic ...) Show SMILES COC(=O)c1c(oc2ccccc2c1=O)-c1ccc(Br)cc1 Show InChI	PDB Reactome pathway UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>2.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Purdue University Curated by ChEMBL					Assay Description Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.				J Med Chem 34: 798-806 (1991) Article DOI: 10.1021/jm00106a047 BindingDB Entry DOI: 10.7270/Q2CF9P3J
Purdue University Curated by ChEMBL					More data for this Ligand-Target Pair
SRC (Homo sapiens (Human))	BDBM50011456 (2-(4-Hydroxy-phenyl)-6-methoxy-4-oxo-4H-chromene-3...) Show SMILES Show InChI	PDB Reactome pathway UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>2.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Purdue University Curated by ChEMBL					Assay Description Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.				J Med Chem 34: 798-806 (1991) Article DOI: 10.1021/jm00106a047 BindingDB Entry DOI: 10.7270/Q2CF9P3J
Purdue University Curated by ChEMBL					More data for this Ligand-Target Pair
SRC (Homo sapiens (Human))	BDBM50011459 (6-Methoxy-2-(4-nitro-phenyl)-4-oxo-4H-chromene-3-c...) Show SMILES Show InChI	PDB Reactome pathway UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>2.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Purdue University Curated by ChEMBL					Assay Description Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.				J Med Chem 34: 798-806 (1991) Article DOI: 10.1021/jm00106a047 BindingDB Entry DOI: 10.7270/Q2CF9P3J
Purdue University Curated by ChEMBL					More data for this Ligand-Target Pair
SRC (Homo sapiens (Human))	BDBM50011462 (3-(2,4-Bis-benzyloxy-6-hydroxy-phenyl)-3-oxo-propi...) Show SMILES Show InChI	PDB Reactome pathway UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>2.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Purdue University Curated by ChEMBL					Assay Description Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.				J Med Chem 34: 798-806 (1991) Article DOI: 10.1021/jm00106a047 BindingDB Entry DOI: 10.7270/Q2CF9P3J
Purdue University Curated by ChEMBL					More data for this Ligand-Target Pair
SRC (Homo sapiens (Human))	BDBM50011443 (2-(3,5-Dimethoxy-phenyl)-4-oxo-4H-chromene-3-carbo...) Show SMILES Show InChI	PDB Reactome pathway UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>2.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Purdue University Curated by ChEMBL					Assay Description Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.				J Med Chem 34: 798-806 (1991) Article DOI: 10.1021/jm00106a047 BindingDB Entry DOI: 10.7270/Q2CF9P3J
Purdue University Curated by ChEMBL					More data for this Ligand-Target Pair
SRC (Homo sapiens (Human))	BDBM50011445 (2-(4-Benzyloxy-phenyl)-7-methoxy-4-oxo-4H-chromene...) Show SMILES Show InChI	PDB Reactome pathway UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>2.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Purdue University Curated by ChEMBL					Assay Description Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.				J Med Chem 34: 798-806 (1991) Article DOI: 10.1021/jm00106a047 BindingDB Entry DOI: 10.7270/Q2CF9P3J
Purdue University Curated by ChEMBL					More data for this Ligand-Target Pair
SRC (Homo sapiens (Human))	BDBM50011452 (2-(4-Methoxy-phenyl)-4-oxo-4H-chromene-3-carboxyli...) Show SMILES COC(=O)c1c(oc2ccccc2c1=O)-c1ccc(OC)cc1 Show InChI	PDB Reactome pathway UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>2.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Purdue University Curated by ChEMBL					Assay Description Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.				J Med Chem 34: 798-806 (1991) Article DOI: 10.1021/jm00106a047 BindingDB Entry DOI: 10.7270/Q2CF9P3J
Purdue University Curated by ChEMBL					More data for this Ligand-Target Pair
SRC (Homo sapiens (Human))	BDBM50011449 (3-(2-Hydroxy-phenyl)-3-oxo-propionic acid methyl e...) Show SMILES COC(=O)CC(=O)c1ccccc1O Show InChI	PDB Reactome pathway UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>2.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Purdue University Curated by ChEMBL					Assay Description Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.				J Med Chem 34: 798-806 (1991) Article DOI: 10.1021/jm00106a047 BindingDB Entry DOI: 10.7270/Q2CF9P3J
Purdue University Curated by ChEMBL					More data for this Ligand-Target Pair
SRC (Homo sapiens (Human))	BDBM50011461 (2-(4-Benzyloxy-phenyl)-4-oxo-4H-chromene-3-carboxy...) Show SMILES Show InChI	PDB Reactome pathway UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>2.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Purdue University Curated by ChEMBL					Assay Description Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.				J Med Chem 34: 798-806 (1991) Article DOI: 10.1021/jm00106a047 BindingDB Entry DOI: 10.7270/Q2CF9P3J
Purdue University Curated by ChEMBL					More data for this Ligand-Target Pair
SRC (Homo sapiens (Human))	BDBM50011430 (4-Oxo-2-(3,4,5-trimethoxy-phenyl)-4H-chromene-3-ca...) Show SMILES Show InChI	PDB Reactome pathway UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	>2.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Purdue University Curated by ChEMBL					Assay Description Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.				J Med Chem 34: 798-806 (1991) Article DOI: 10.1021/jm00106a047 BindingDB Entry DOI: 10.7270/Q2CF9P3J
Purdue University Curated by ChEMBL					More data for this Ligand-Target Pair
SRC (Homo sapiens (Human))	BDBM50011436 (5,7-Dihydroxy-2-(4-nitro-phenyl)-4-oxo-4H-chromene...) Show SMILES Show InChI	PDB Reactome pathway UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>2.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Purdue University Curated by ChEMBL					Assay Description Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.				J Med Chem 34: 798-806 (1991) Article DOI: 10.1021/jm00106a047 BindingDB Entry DOI: 10.7270/Q2CF9P3J
Purdue University Curated by ChEMBL					More data for this Ligand-Target Pair
SRC (Homo sapiens (Human))	BDBM50011439 (2-(3,5-Dimethoxy-phenyl)-4-oxo-4H-chromene-3-carbo...) Show SMILES Show InChI	PDB Reactome pathway UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>2.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Purdue University Curated by ChEMBL					Assay Description Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.				J Med Chem 34: 798-806 (1991) Article DOI: 10.1021/jm00106a047 BindingDB Entry DOI: 10.7270/Q2CF9P3J
Purdue University Curated by ChEMBL					More data for this Ligand-Target Pair
SRC (Homo sapiens (Human))	BDBM50011440 (2-(4-Nitro-phenyl)-4-oxo-4H-chromene-3-carboxylic ...) Show SMILES Show InChI	PDB Reactome pathway UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>2.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Purdue University Curated by ChEMBL					Assay Description Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.				J Med Chem 34: 798-806 (1991) Article DOI: 10.1021/jm00106a047 BindingDB Entry DOI: 10.7270/Q2CF9P3J
Purdue University Curated by ChEMBL					More data for this Ligand-Target Pair
SRC (Homo sapiens (Human))	BDBM50011442 (6-Hydroxy-2-(4-nitro-phenyl)-chromen-4-one \| 6-hyd...) Show SMILES Show InChI	PDB Reactome pathway UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	>2.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Purdue University Curated by ChEMBL					Assay Description Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.				J Med Chem 34: 798-806 (1991) Article DOI: 10.1021/jm00106a047 BindingDB Entry DOI: 10.7270/Q2CF9P3J
Purdue University Curated by ChEMBL					More data for this Ligand-Target Pair
SRC (Homo sapiens (Human))	BDBM50011454 (2-(4-Benzyloxy-phenyl)-6-methoxy-4-oxo-4H-chromene...) Show SMILES Show InChI	PDB Reactome pathway UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>2.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Purdue University Curated by ChEMBL					Assay Description Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.				J Med Chem 34: 798-806 (1991) Article DOI: 10.1021/jm00106a047 BindingDB Entry DOI: 10.7270/Q2CF9P3J
Purdue University Curated by ChEMBL					More data for this Ligand-Target Pair
SRC (Homo sapiens (Human))	BDBM50011457 (2-(4-Nitro-phenyl)-4-oxo-4H-chromene-3-carboxylic ...) Show SMILES Show InChI	PDB Reactome pathway UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>2.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Purdue University Curated by ChEMBL					Assay Description Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.				J Med Chem 34: 798-806 (1991) Article DOI: 10.1021/jm00106a047 BindingDB Entry DOI: 10.7270/Q2CF9P3J
Purdue University Curated by ChEMBL					More data for this Ligand-Target Pair
SRC (Homo sapiens (Human))	BDBM50011450 (2-(4-Bromo-phenyl)-4-oxo-4H-chromene-3-carboxylic ...) Show SMILES OC(=O)c1c(oc2ccccc2c1=O)-c1ccc(Br)cc1 Show InChI	PDB Reactome pathway UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>2.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Purdue University Curated by ChEMBL					Assay Description Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.				J Med Chem 34: 798-806 (1991) Article DOI: 10.1021/jm00106a047 BindingDB Entry DOI: 10.7270/Q2CF9P3J
Purdue University Curated by ChEMBL					More data for this Ligand-Target Pair
SRC (Homo sapiens (Human))	BDBM50011417 (5,7-Dihydroxy-2-(4-nitro-phenyl)-chromen-4-one \| 5...) Show SMILES Show InChI	PDB Reactome pathway UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>2.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Purdue University Curated by ChEMBL					Assay Description Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.				J Med Chem 34: 798-806 (1991) Article DOI: 10.1021/jm00106a047 BindingDB Entry DOI: 10.7270/Q2CF9P3J
Purdue University Curated by ChEMBL					More data for this Ligand-Target Pair
SRC (Homo sapiens (Human))	BDBM50011420 (7-Methoxy-2-(4-nitro-phenyl)-4-oxo-4H-chromene-3-c...) Show SMILES Show InChI	PDB Reactome pathway UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>2.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Purdue University Curated by ChEMBL					Assay Description Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.				J Med Chem 34: 798-806 (1991) Article DOI: 10.1021/jm00106a047 BindingDB Entry DOI: 10.7270/Q2CF9P3J
Purdue University Curated by ChEMBL					More data for this Ligand-Target Pair
SRC (Homo sapiens (Human))	BDBM50011447 (4-Oxo-2-(3,4,5-trimethoxy-phenyl)-4H-chromene-3-ca...) Show SMILES Show InChI	PDB Reactome pathway UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>2.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Purdue University Curated by ChEMBL					Assay Description Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.				J Med Chem 34: 798-806 (1991) Article DOI: 10.1021/jm00106a047 BindingDB Entry DOI: 10.7270/Q2CF9P3J
Purdue University Curated by ChEMBL					More data for this Ligand-Target Pair
SRC (Homo sapiens (Human))	BDBM50011431 (2-(4-Acetylamino-phenyl)-6-methoxy-4-oxo-4H-chrome...) Show SMILES Show InChI	PDB Reactome pathway UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>2.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Purdue University Curated by ChEMBL					Assay Description Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.				J Med Chem 34: 798-806 (1991) Article DOI: 10.1021/jm00106a047 BindingDB Entry DOI: 10.7270/Q2CF9P3J
Purdue University Curated by ChEMBL					More data for this Ligand-Target Pair
SRC (Homo sapiens (Human))	BDBM50011421 (2-(4-Nitro-phenyl)-chromen-4-one \| CHEMBL64780) Show SMILES Show InChI	PDB Reactome pathway UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar	Purchase CHEMBL MMDB PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	>2.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Purdue University Curated by ChEMBL					Assay Description Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.				J Med Chem 34: 798-806 (1991) Article DOI: 10.1021/jm00106a047 BindingDB Entry DOI: 10.7270/Q2CF9P3J
Purdue University Curated by ChEMBL					More data for this Ligand-Target Pair
SRC (Homo sapiens (Human))	BDBM50011415 (3-(2-Hydroxy-phenyl)-3-oxo-propionic acid ethyl es...) Show SMILES CCOC(=O)CC(=O)c1ccccc1O Show InChI	PDB Reactome pathway UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>2.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Purdue University Curated by ChEMBL					Assay Description Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.				J Med Chem 34: 798-806 (1991) Article DOI: 10.1021/jm00106a047 BindingDB Entry DOI: 10.7270/Q2CF9P3J
Purdue University Curated by ChEMBL					More data for this Ligand-Target Pair
SRC (Homo sapiens (Human))	BDBM50011453 (3-Oxo-3-(2,3,4-trihydroxy-phenyl)-propionic acid m...) Show SMILES COC(=O)CC(=O)c1ccc(O)c(O)c1O Show InChI	PDB Reactome pathway UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>2.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Purdue University Curated by ChEMBL					Assay Description Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.				J Med Chem 34: 798-806 (1991) Article DOI: 10.1021/jm00106a047 BindingDB Entry DOI: 10.7270/Q2CF9P3J
Purdue University Curated by ChEMBL					More data for this Ligand-Target Pair
SRC (Homo sapiens (Human))	BDBM50011428 (2-(3,4,5-Trimethoxy-phenyl)-chromen-4-one \| 2-(3,4...) Show SMILES COc1cc(cc(OC)c1OC)-c1cc(=O)c2ccccc2o1 Show InChI	PDB Reactome pathway UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	>2.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Purdue University Curated by ChEMBL					Assay Description Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.				J Med Chem 34: 798-806 (1991) Article DOI: 10.1021/jm00106a047 BindingDB Entry DOI: 10.7270/Q2CF9P3J
Purdue University Curated by ChEMBL					More data for this Ligand-Target Pair
SRC (Homo sapiens (Human))	BDBM50011444 (7-Methoxy-2-(4-nitro-phenyl)-4-oxo-4H-chromene-3-c...) Show SMILES Show InChI	PDB Reactome pathway UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>2.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Purdue University Curated by ChEMBL					Assay Description Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.				J Med Chem 34: 798-806 (1991) Article DOI: 10.1021/jm00106a047 BindingDB Entry DOI: 10.7270/Q2CF9P3J
Purdue University Curated by ChEMBL					More data for this Ligand-Target Pair
SRC (Homo sapiens (Human))	BDBM50011433 (3-(2,4-Bis-benzyloxy-6-hydroxy-phenyl)-3-oxo-propi...) Show SMILES Show InChI	PDB Reactome pathway UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>2.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Purdue University Curated by ChEMBL					Assay Description Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.				J Med Chem 34: 798-806 (1991) Article DOI: 10.1021/jm00106a047 BindingDB Entry DOI: 10.7270/Q2CF9P3J
Purdue University Curated by ChEMBL					More data for this Ligand-Target Pair
SRC (Homo sapiens (Human))	BDBM50011423 (5,7-Bis-benzyloxy-2-(4-nitro-phenyl)-4-oxo-4H-chro...) Show SMILES Show InChI	PDB Reactome pathway UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>2.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Purdue University Curated by ChEMBL					Assay Description Ability to inhibit protein-tyrosine kinase activity of p56lck (isolated from bovine thymus) in vitro.				J Med Chem 34: 798-806 (1991) Article DOI: 10.1021/jm00106a047 BindingDB Entry DOI: 10.7270/Q2CF9P3J
Purdue University Curated by ChEMBL					More data for this Ligand-Target Pair

* indicates data uncertainty>20%