BDBM50011438 2-(4-Amino-phenyl)-7-hydroxy-chromen-4-one::2-(4-aminophenyl)-7-hydroxy-4H-chromen-4-one::7-Hydroxy-flavone, 6::CHEMBL165751
SMILES: Nc1ccc(cc1)-c1cc(=O)c2ccc(O)cc2o1
InChI Key: InChIKey=MYNFUICRGYXJID-UHFFFAOYSA-N
Data: 3 IC50
Target/Host (Institution) | Ligand | Target/Host Links | Ligand Links | Trg + Lig Links | Ki nM | ΔG° kcal/mole | IC50 nM | Kd nM | EC50/IC50 nM | koff s-1 | kon M-1s-1 | pH | Temp °C |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Cytochrome P450 19A1 (Homo sapiens (Human)) | BDBM50011438 (2-(4-Amino-phenyl)-7-hydroxy-chromen-4-one | 2-(4-...) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | >2.00E+4 | n/a | n/a | n/a | n/a | n/a | 37 |
Cardiff University | Assay Description The classical 3H2O assay was used to measure the effect of the flavones on aromatase activity using human placental microsomes. | J Enzym Inhib 16: 417-24 (2001) Article DOI: 10.1080/14756360109162390 BindingDB Entry DOI: 10.7270/Q2FJ2FBS | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Tyrosine-protein kinase Lck (Homo sapiens (Human)) | BDBM50011438 (2-(4-Amino-phenyl)-7-hydroxy-chromen-4-one | 2-(4-...) | PDB UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 1 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA Curated by ChEMBL | Assay Description Inhibition of p56 lck | J Nat Prod 55: 1529-1560 (1992) Article DOI: 10.1021/np50089a001 BindingDB Entry DOI: 10.7270/Q2J966CC | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Tyrosine-protein kinase Lck (Homo sapiens (Human)) | BDBM50011438 (2-(4-Amino-phenyl)-7-hydroxy-chromen-4-one | 2-(4-...) | PDB UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | 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) BindingDB Entry DOI: 10.7270/Q2CF9P3J | |||||||||||
More data for this Ligand-Target Pair |