BDBM50093539 7,8-Dihydroxy-2-phenyl-chromen-4-one::7,8-Dihydroxyflavone::7,8-dihydroxy-2-phenyl-4H-chromen-4-one::CHEMBL75267
SMILES Oc1ccc2c(oc(cc2=O)-c2ccccc2)c1O
InChI Key InChIKey=COCYGNDCWFKTMF-UHFFFAOYSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 6 hits for monomerid = 50093539
Affinity DataIC50: 3.14E+5nMAssay Description:Inhibition of p56 lckMore data for this Ligand-Target Pair
TargetTelomerase reverse transcriptase(Homo sapiens (Human))
Bu-Nerviano Medical Sciences
Curated by ChEMBL
Bu-Nerviano Medical Sciences
Curated by ChEMBL
Affinity DataIC50: 3.60E+4nMAssay Description:Inhibition of human telomerase from HEK293 cell extracts by Flash-Plate assayMore data for this Ligand-Target Pair
TargetBDNF/NT-3 growth factors receptor(Homo sapiens (Human))
National Cheng Kung University
Curated by ChEMBL
National Cheng Kung University
Curated by ChEMBL
Affinity DataKd: 10nMAssay Description:Binding affinity to recombinant human TrkB receptor ECD assessed as dissociation constantMore data for this Ligand-Target Pair
TargetBDNF/NT-3 growth factors receptor(Homo sapiens (Human))
National Cheng Kung University
Curated by ChEMBL
National Cheng Kung University
Curated by ChEMBL
Affinity DataKd: 320nMAssay Description:Binding affinity to TrkB receptor extracellular domain (unknown origin) after 10 mins by liquid Scatchard plot analysisMore data for this Ligand-Target Pair
Affinity DataIC50: 3.50E+5nMAssay Description:In vitro antibacterial activity was determined as inhibitory concentration causing 50% DNA-gyrase supercoiling inhibition (SCI)More data for this Ligand-Target Pair
TargetInhibitor of nuclear factor kappa-B kinase subunit beta(Homo sapiens (Human))
China Pharmaceutical University
Curated by ChEMBL
China Pharmaceutical University
Curated by ChEMBL
Affinity DataIC50: 9.82E+3nMAssay Description:Inhibition of IKK-beta using TMB substrate after 15 mins by spectrophotometer analysisMore data for this Ligand-Target Pair