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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
SRC (Homo sapiens (Human)) | BDBM50011418![]() (2-(4-Amino-phenyl)-6-hydroxy-chromen-4-one | 2-(4-...) | 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 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
SRC (Homo sapiens (Human)) | BDBM50011429![]() (2-(4-Amino-phenyl)-5,7-dihydroxy-chromen-4-one | 2...) | 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 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
SRC (Homo sapiens (Human)) | BDBM7460![]() (2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-4H-chrome...) | 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 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
SRC (Homo sapiens (Human)) | BDBM50011424![]() (2-(4-Hydroxy-3,5-dimethoxy-phenyl)-chromen-4-one |...) | 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 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
SRC (Homo sapiens (Human)) | BDBM50011438![]() (2-(4-Amino-phenyl)-7-hydroxy-chromen-4-one | 2-(4-...) | 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 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
SRC (Homo sapiens (Human)) | BDBM50011437![]() (2-(4-Amino-phenyl)-chromen-4-one | 2-(4-aminopheny...) | 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 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
SRC (Homo sapiens (Human)) | BDBM50011455![]() (2-(4-Hydroxy-phenyl)-4-oxo-4H-chromene-3-carboxyli...) | 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 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
SRC (Homo sapiens (Human)) | BDBM50011446![]() (2-(4-Hydroxy-phenyl)-chromen-4-one | 2-(4-hydroxyp...) | 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 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
SRC (Homo sapiens (Human)) | BDBM50011416![]() (2-(4-Amino-phenyl)-4-oxo-4H-chromene-3-carboxylic ...) | 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 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
SRC (Homo sapiens (Human)) | BDBM50011422![]() (2-(4-Hydroxy-phenyl)-7-methoxy-4-oxo-4H-chromene-3...) | 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 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
SRC (Homo sapiens (Human)) | BDBM50011451![]() (3-(2-Hydroxy-4-methoxy-phenyl)-3-oxo-propionic aci...) | 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 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
SRC (Homo sapiens (Human)) | BDBM50011458![]() (2-(4-Hydroxy-phenyl)-4-oxo-4H-chromene-3-carboxyli...) | 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 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
SRC (Homo sapiens (Human)) | BDBM50011419![]() (6-Methoxy-2-(4-nitro-phenyl)-4-oxo-4H-chromene-3-c...) | 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 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
SRC (Homo sapiens (Human)) | BDBM50011426![]() (2-(4-Hydroxy-phenyl)-7-methoxy-4-oxo-4H-chromene-3...) | 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 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
SRC (Homo sapiens (Human)) | BDBM50011427![]() (7-Hydroxy-2-(4-nitro-phenyl)-chromen-4-one | 7-hyd...) | 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 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
SRC (Homo sapiens (Human)) | BDBM50011435![]() (3-(2-Hydroxy-5-methoxy-phenyl)-3-oxo-propionic aci...) | 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 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
SRC (Homo sapiens (Human)) | BDBM50011441![]() (2-(4-Methoxy-phenyl)-4-oxo-4H-chromene-3-carboxyli...) | 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 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
SRC (Homo sapiens (Human)) | BDBM50011448![]() (4-Oxo-2-[4-(3,4,5-trimethoxy-benzoylamino)-phenyl]...) | 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 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
SRC (Homo sapiens (Human)) | BDBM50011460![]() (2-(4-Acetylamino-phenyl)-7-methoxy-4-oxo-4H-chrome...) | 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 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
SRC (Homo sapiens (Human)) | BDBM50011425![]() (2-(3,4-Dimethoxy-phenyl)-4-oxo-4H-chromene-3-carbo...) | 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 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
SRC (Homo sapiens (Human)) | BDBM50011432![]() (2-(3,4-Dimethoxy-phenyl)-4-oxo-4H-chromene-3-carbo...) | 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 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
SRC (Homo sapiens (Human)) | BDBM50011434![]() (2-(4-Bromo-phenyl)-4-oxo-4H-chromene-3-carboxylic ...) | 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 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
SRC (Homo sapiens (Human)) | BDBM50011456![]() (2-(4-Hydroxy-phenyl)-6-methoxy-4-oxo-4H-chromene-3...) | 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 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
SRC (Homo sapiens (Human)) | BDBM50011459![]() (6-Methoxy-2-(4-nitro-phenyl)-4-oxo-4H-chromene-3-c...) | 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 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
SRC (Homo sapiens (Human)) | BDBM50011462![]() (3-(2,4-Bis-benzyloxy-6-hydroxy-phenyl)-3-oxo-propi...) | 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 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
SRC (Homo sapiens (Human)) | BDBM50011443![]() (2-(3,5-Dimethoxy-phenyl)-4-oxo-4H-chromene-3-carbo...) | 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 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
SRC (Homo sapiens (Human)) | BDBM50011445![]() (2-(4-Benzyloxy-phenyl)-7-methoxy-4-oxo-4H-chromene...) | 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 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
SRC (Homo sapiens (Human)) | BDBM50011452![]() (2-(4-Methoxy-phenyl)-4-oxo-4H-chromene-3-carboxyli...) | 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 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
SRC (Homo sapiens (Human)) | BDBM50011449![]() (3-(2-Hydroxy-phenyl)-3-oxo-propionic acid methyl e...) | 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 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
SRC (Homo sapiens (Human)) | BDBM50011461![]() (2-(4-Benzyloxy-phenyl)-4-oxo-4H-chromene-3-carboxy...) | 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 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
SRC (Homo sapiens (Human)) | BDBM50011430![]() (4-Oxo-2-(3,4,5-trimethoxy-phenyl)-4H-chromene-3-ca...) | 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 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
SRC (Homo sapiens (Human)) | BDBM50011436![]() (5,7-Dihydroxy-2-(4-nitro-phenyl)-4-oxo-4H-chromene...) | 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 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
SRC (Homo sapiens (Human)) | BDBM50011439![]() (2-(3,5-Dimethoxy-phenyl)-4-oxo-4H-chromene-3-carbo...) | 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 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
SRC (Homo sapiens (Human)) | BDBM50011440![]() (2-(4-Nitro-phenyl)-4-oxo-4H-chromene-3-carboxylic ...) | 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 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
SRC (Homo sapiens (Human)) | BDBM50011442![]() (6-Hydroxy-2-(4-nitro-phenyl)-chromen-4-one | 6-hyd...) | 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 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
SRC (Homo sapiens (Human)) | BDBM50011454![]() (2-(4-Benzyloxy-phenyl)-6-methoxy-4-oxo-4H-chromene...) | 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 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
SRC (Homo sapiens (Human)) | BDBM50011457![]() (2-(4-Nitro-phenyl)-4-oxo-4H-chromene-3-carboxylic ...) | 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 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
SRC (Homo sapiens (Human)) | BDBM50011450![]() (2-(4-Bromo-phenyl)-4-oxo-4H-chromene-3-carboxylic ...) | 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 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
SRC (Homo sapiens (Human)) | BDBM50011417![]() (5,7-Dihydroxy-2-(4-nitro-phenyl)-chromen-4-one | 5...) | 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 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
SRC (Homo sapiens (Human)) | BDBM50011420![]() (7-Methoxy-2-(4-nitro-phenyl)-4-oxo-4H-chromene-3-c...) | 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 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
SRC (Homo sapiens (Human)) | BDBM50011447![]() (4-Oxo-2-(3,4,5-trimethoxy-phenyl)-4H-chromene-3-ca...) | 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 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
SRC (Homo sapiens (Human)) | BDBM50011431![]() (2-(4-Acetylamino-phenyl)-6-methoxy-4-oxo-4H-chrome...) | 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 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
SRC (Homo sapiens (Human)) | BDBM50011421![]() (2-(4-Nitro-phenyl)-chromen-4-one | CHEMBL64780) | 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 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
SRC (Homo sapiens (Human)) | BDBM50011415![]() (3-(2-Hydroxy-phenyl)-3-oxo-propionic acid ethyl es...) | 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 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
SRC (Homo sapiens (Human)) | BDBM50011453![]() (3-Oxo-3-(2,3,4-trihydroxy-phenyl)-propionic acid m...) | 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 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
SRC (Homo sapiens (Human)) | BDBM50011428![]() (2-(3,4,5-Trimethoxy-phenyl)-chromen-4-one | 2-(3,4...) | 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 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
SRC (Homo sapiens (Human)) | BDBM50011444![]() (7-Methoxy-2-(4-nitro-phenyl)-4-oxo-4H-chromene-3-c...) | 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 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
SRC (Homo sapiens (Human)) | BDBM50011433![]() (3-(2,4-Bis-benzyloxy-6-hydroxy-phenyl)-3-oxo-propi...) | 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 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
SRC (Homo sapiens (Human)) | BDBM50011423![]() (5,7-Bis-benzyloxy-2-(4-nitro-phenyl)-4-oxo-4H-chro...) | 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 | |||||||||||
More data for this Ligand-Target Pair |