null

SMILES CN1CN(C\C=C\C(O)=O)C(=O)N[C@@H](Cc2ccccc2)C1=O

InChI Key InChIKey=KTSVVWZTTDBBMX-LJLILKBBSA-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 2 hits for monomerid = 50200327   

TargetGroup 10 secretory phospholipase A2(Homo sapiens (Human))
CNRS UMR 7175

Curated by ChEMBL
LigandPNGBDBM50200327((E)-4-(6-Benzyl-1-methyl-4,7-dioxo-[1,3,5]triazepa...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human group 10 sPLA2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2PNDPubMed
TargetPhospholipase A2 group V(Homo sapiens (Human))
CNRS UMR 7175

Curated by ChEMBL
LigandPNGBDBM50200327((E)-4-(6-Benzyl-1-methyl-4,7-dioxo-[1,3,5]triazepa...)copy SMILEScopy InChI
Affinity DataIC50: 1.20E+4nMAssay Description:Inhibition of human group 5 sPLA2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WH2PNDPubMed