null

SMILES Fc1ccc(\C=N\OC(=O)c2ccccc2)cc1F

InChI Key InChIKey=HOHACQRGFZUDCD-RQZCQDPDSA-N

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

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50161743   

TargetPlatelet-activating factor acetylhydrolase(Homo sapiens (Human))
National Research Laboratory of Lipid Metabolism and Atherosclerosis

Curated by ChEMBL
LigandPNGBDBM50161743(3,4-difluorobenzaldehyde O-benzoyloxime | CHEMBL17...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+3nMAssay Description:Inhibition of human Low density lipoprotein-associated phospholipase A2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TM79RHPubMed
TargetPlatelet-activating factor acetylhydrolase(Homo sapiens (Human))
National Research Laboratory of Lipid Metabolism and Atherosclerosis

Curated by ChEMBL
LigandPNGBDBM50161743(3,4-difluorobenzaldehyde O-benzoyloxime | CHEMBL17...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+3nMAssay Description:In vitro inhibitory activity against human lipoprotein-associated phospholiphase A2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28915CKPubMed