null

SMILES CCc1c(C(=O)C(N)=O)c2c(OCC(=O)NS(=O)(=O)c3ccccc3)cc3ccccc3c2n1Cc1ccccc1

InChI Key InChIKey=OPNVDNPKPOZEDE-UHFFFAOYSA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 14 hits for monomerid = 50263000   

TargetPhospholipase A2(Homo sapiens (Human))
University of Washington

Curated by ChEMBL
LigandPNGBDBM50263000(2-(1-benzyl-2-ethyl-1H-6,7-benzoindol-4-yloxy)-N-(...)copy SMILEScopy InChI
Affinity DataIC50: 1.30E+3nMAssay Description:Inhibition of human group1B phospholipase A2 fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2571BSDPubMed
TargetPhospholipase A2(Mus musculus)
University of Washington

Curated by ChEMBL
LigandPNGBDBM50263000(2-(1-benzyl-2-ethyl-1H-6,7-benzoindol-4-yloxy)-N-(...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:Inhibition of mouse group1B phospholipase A2 fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2571BSDPubMed
TargetPhospholipase A2, membrane associated(Homo sapiens (Human))
University of Washington

Curated by ChEMBL
LigandPNGBDBM50263000(2-(1-benzyl-2-ethyl-1H-6,7-benzoindol-4-yloxy)-N-(...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:Inhibition of human group2A phospholipase A2 fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2571BSDPubMed
TargetPhospholipase A2, membrane associated(Mus musculus)
University of Washington

Curated by ChEMBL
LigandPNGBDBM50263000(2-(1-benzyl-2-ethyl-1H-6,7-benzoindol-4-yloxy)-N-(...)copy SMILEScopy InChI
Affinity DataIC50: 90nMAssay Description:Inhibition of mouse group2A phospholipase A2 fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2571BSDPubMed
TargetGroup IID secretory phospholipase A2(Homo sapiens (Human))
University of Washington

Curated by ChEMBL
LigandPNGBDBM50263000(2-(1-benzyl-2-ethyl-1H-6,7-benzoindol-4-yloxy)-N-(...)copy SMILEScopy InChI
Affinity DataIC50: 35nMAssay Description:Inhibition of human group2D phospholipase A2 by [3H]oleic acid-labeled Escherichia coli membrane assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2571BSDPubMed
TargetGroup IID secretory phospholipase A2(Mus musculus)
University of Washington

Curated by ChEMBL
LigandPNGBDBM50263000(2-(1-benzyl-2-ethyl-1H-6,7-benzoindol-4-yloxy)-N-(...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of mouse group2D phospholipase A2 fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2571BSDPubMed
TargetGroup 10 secretory phospholipase A2(Mus musculus)
University of Washington

Curated by ChEMBL
LigandPNGBDBM50263000(2-(1-benzyl-2-ethyl-1H-6,7-benzoindol-4-yloxy)-N-(...)copy SMILEScopy InChI
Affinity DataIC50: 35nMAssay Description:Inhibition of mouse group2X phospholipase A2 fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2571BSDPubMed
TargetGroup IIE secretory phospholipase A2(Mus musculus)
University of Washington

Curated by ChEMBL
LigandPNGBDBM50263000(2-(1-benzyl-2-ethyl-1H-6,7-benzoindol-4-yloxy)-N-(...)copy SMILEScopy InChI
Affinity DataIC50: 48nMAssay Description:Inhibition of mouse group2E phospholipase A2 fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2571BSDPubMed
TargetGroup IIF secretory phospholipase A2(Homo sapiens (Human))
University of Washington

Curated by ChEMBL
LigandPNGBDBM50263000(2-(1-benzyl-2-ethyl-1H-6,7-benzoindol-4-yloxy)-N-(...)copy SMILEScopy InChI
Affinity DataIC50: 550nMAssay Description:Inhibition of human group2F phospholipase A2 fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2571BSDPubMed
TargetGroup IIF secretory phospholipase A2(Mus musculus)
University of Washington

Curated by ChEMBL
LigandPNGBDBM50263000(2-(1-benzyl-2-ethyl-1H-6,7-benzoindol-4-yloxy)-N-(...)copy SMILEScopy InChI
Affinity DataIC50: 1.60E+3nMAssay Description:Inhibition of mouse group2F phospholipase A2 fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2571BSDPubMed
TargetPhospholipase A2 group V(Homo sapiens (Human))
University of Washington

Curated by ChEMBL
LigandPNGBDBM50263000(2-(1-benzyl-2-ethyl-1H-6,7-benzoindol-4-yloxy)-N-(...)copy SMILEScopy InChI
Affinity DataIC50: 140nMAssay Description:Inhibition of human group2V phospholipase A2 fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2571BSDPubMed
TargetPhospholipase A2 group V(Mus musculus)
University of Washington

Curated by ChEMBL
LigandPNGBDBM50263000(2-(1-benzyl-2-ethyl-1H-6,7-benzoindol-4-yloxy)-N-(...)copy SMILEScopy InChI
Affinity DataIC50: 70nMAssay Description:Inhibition of mouse group2V phospholipase A2 fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2571BSDPubMed
TargetGroup 10 secretory phospholipase A2(Homo sapiens (Human))
University of Washington

Curated by ChEMBL
LigandPNGBDBM50263000(2-(1-benzyl-2-ethyl-1H-6,7-benzoindol-4-yloxy)-N-(...)copy SMILEScopy InChI
Affinity DataIC50: 90nMAssay Description:Inhibition of human group2X phospholipase A2 fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2571BSDPubMed
TargetGroup IIE secretory phospholipase A2(Homo sapiens (Human))
University of Washington

Curated by ChEMBL
LigandPNGBDBM50263000(2-(1-benzyl-2-ethyl-1H-6,7-benzoindol-4-yloxy)-N-(...)copy SMILEScopy InChI
Affinity DataIC50: 16nMAssay Description:Inhibition of human group2E phospholipase A2 fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2571BSDPubMed