null

SMILES C[C@@H]1O[C@@H](O[C@H]2Cc3c(O)cc(O)cc3O[C@@H]2c2ccc(O)cc2)[C@H](O)[C@H](O)[C@H]1O

InChI Key InChIKey=SQJLTDFIOMWZDE-QUYVSAIISA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50269600   

TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
University of Illinois at Chicago

Curated by ChEMBL
LigandPNGBDBM50269600(CHEMBL517149 | afzelechin-3-O-alpha-Lrhamnopyranos...)copy SMILEScopy InChI
Affinity DataIC50: 1.97E+4nMAssay Description:Inhibition of COX2More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2J38TGVPubMed
TargetProstaglandin G/H synthase 1(Homo sapiens (Human))
University of Illinois at Chicago

Curated by ChEMBL
LigandPNGBDBM50269600(CHEMBL517149 | afzelechin-3-O-alpha-Lrhamnopyranos...)copy SMILEScopy InChI
Affinity DataIC50: 8.30E+3nMAssay Description:Inhibition of COX1More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2J38TGVPubMed