null

SMILES COc1ccccc1-n1c(O)c2C(OC3(C(=O)c4ccccc4C3=O)c2c1O)c1ccccc1C

InChI Key InChIKey=WKIPIHOSPIAZQO-UHFFFAOYSA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50140708   

TargetPhenylalanine--tRNA ligase, mitochondrial(Homo sapiens (Human))
Cubist Pharmaceuticals Inc.

Curated by ChEMBL
LigandPNGBDBM50140708(5-(2-methoxyphenyl)-3-(2-methylphenyl)-(3R,3aS,6aR...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibitory activity against human phenylalanyl-tRNA synthetase was determinedMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR7VDSPubMed
TargetPhenylalanine--tRNA ligase alpha subunit(Streptococcus pyogenes serotype M18)
Cubist Pharmaceuticals Inc.

Curated by ChEMBL
LigandPNGBDBM50140708(5-(2-methoxyphenyl)-3-(2-methylphenyl)-(3R,3aS,6aR...)copy SMILEScopy InChI
Affinity DataIC50: 5.70E+4nMAssay Description:Inhibitory activity against human phenylalanyl-tRNA synthetase was determinedMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR7VDSPubMed
TargetPhenylalanine--tRNA ligase alpha subunit(Streptococcus pyogenes serotype M18)
Cubist Pharmaceuticals Inc.

Curated by ChEMBL
LigandPNGBDBM50140708(5-(2-methoxyphenyl)-3-(2-methylphenyl)-(3R,3aS,6aR...)copy SMILEScopy InChI
Affinity DataIC50: 1.30E+4nMAssay Description:Inhibitory activity against phenylalanyl-tRNA synthetase from Staphylococcus aureusMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR7VDSPubMed