BDBM61566 (4E)-4-[[2-[2-(2-fluorophenyl)quinazolin-4-yl]hydrazinyl]methylidene]-3-hydroxycyclohexa-2,5-dien-1-one::(4E)-4-[[2-[2-(2-fluorophenyl)quinazolin-4-yl]hydrazinyl]methylidene]-3-oxidanyl-cyclohexa-2,5-dien-1-one::(4E)-4-[[N'-[2-(2-fluorophenyl)quinazolin-4-yl]hydrazino]methylene]-3-hydroxy-cyclohexa-2,5-dien-1-one::(4E)-4-[[[2-(2-fluorophenyl)-4-quinazolinyl]hydrazo]methylidene]-3-hydroxy-1-cyclohexa-2,5-dienone::4-{[2-(2-Fluoro-phenyl)-quinazolin-4-yl]-hydrazonomethyl}-benzene-1,3-diol::MLS000778210::SMR000414892::cid_16682714
SMILES Oc1ccc(CN=Nc2nc(nc3ccccc23)-c2ccccc2F)c(O)c1
InChI Key InChIKey=BDKQGMJNSVBBLT-UHFFFAOYSA-N
Data 2 IC50
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 2 hits for monomerid = 61566
TargetG-protein coupled receptor 35(Homo sapiens (Human))
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Affinity DataIC50: 3.08E+3nMAssay Description:Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute (SBMRI, San Diego, C...More data for this Ligand-Target Pair
TargetG-protein coupled receptor 55(Homo sapiens (Human))
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Affinity DataIC50: 1.47E+3nMAssay Description:Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute (SBMRI, San Diego, C...More data for this Ligand-Target Pair