BDBM76112 (3E)-6-hexyl-3-[5-(3,4,5-trimethoxyphenyl)-3H-1,3,4-oxadiazol-2-ylidene]-1-benzopyran-2,7-dione::(3E)-6-hexyl-3-[5-(3,4,5-trimethoxyphenyl)-3H-1,3,4-oxadiazol-2-ylidene]chromene-2,7-dione::(3E)-6-hexyl-3-[5-(3,4,5-trimethoxyphenyl)-3H-1,3,4-oxadiazol-2-ylidene]chromene-2,7-quinone::6-Hexyl-7-hydroxy-3-[5-(3,4,5-trimethoxy-phenyl)-[1,3,4]oxadiazol-2-yl]-chromen-2-one::MLS000035473::SMR000123070::cid_9549343
SMILES CCCCCCC1=Cc2c\c(=C3\NN=C(O3)c3cc(OC)c(OC)c(OC)c3)c(=O)oc2=CC1=O
InChI Key InChIKey=ZIVHMAVCUVECIJ-XIEYBQDHSA-N
Data 2 EC50
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 2 hits for monomerid = 76112
TargetApelin receptor(Homo sapiens (Human))
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Affinity DataEC50: >1.00E+5nMAssay Description:Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute(SBMRI, San Diego) Ne...More data for this Ligand-Target Pair
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 DataEC50: >1.00E+5nMAssay Description:Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute(SBMRI, San Diego) Ne...More data for this Ligand-Target Pair