BDBM67166 (2R,3R)-2-(3-bromanyl-4-methoxy-phenyl)-6-methoxy-3-oxidanyl-2,3-dihydrochromen-4-one::(2R,3R)-2-(3-bromo-4-methoxy-phenyl)-3-hydroxy-6-methoxy-chroman-4-one::(2R,3R)-2-(3-bromo-4-methoxyphenyl)-3-hydroxy-6-methoxy-2,3-dihydrochromen-4-one::(2R,3R)-2-(3-bromo-4-methoxyphenyl)-3-hydroxy-6-methoxy-3,4-dihydro-2H-1-benzopyran-4-one::MLS000438767::SMR000113160::cid_6917582
SMILES COc1ccc2O[C@@H](C(=O)C(O)c2c1)c1ccc(OC)c(Br)c1
InChI Key InChIKey=VNARNCLQMGHYSY-OMOCHNIRSA-N
Data 2 IC50
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 2 hits for monomerid = 67166
TargetType-1 angiotensin II receptor(Homo sapiens (Human))
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Affinity DataIC50: 1.21E+4nMAssay 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
TargetApelin receptor(Homo sapiens (Human))
Sanford-Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Sanford-Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Affinity DataIC50: 3.07E+3nMAssay Description:Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford- Sanford-Burnham Medical Research Institute(SBMRI, San...More data for this Ligand-Target Pair