null

SMILES Cl.Cl.CC1=CC2CC(C1)c1c(C2)nc2cc(Cl)ccc2c1NCCCCCCCNC(=O)[C@@H](N)Cc1c[nH]c2ccccc12

InChI Key

  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 3 hits for monomerid = 50571190   

TargetAcetylcholinesterase(Homo sapiens (Human))TBA
LigandPNGBDBM50571190(CHEMBL4878434)copy SMILES
Affinity DataIC50: 12nMAssay Description:Inhibition of recombinant human AChE using acetylthiocholine as substrate by DTNB-reagent based Ellman's methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WD44BGPubMed
TargetNitric oxide synthase, brain(Homo sapiens (Human))TBA
LigandPNGBDBM50571190(CHEMBL4878434)copy SMILES
Affinity DataIC50: 3.50E+4nMAssay Description:Inhibition of recombinant human nNOSMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WD44BGPubMed
TargetCholinesterase(Homo sapiens (Human))TBA
LigandPNGBDBM50571190(CHEMBL4878434)copy SMILES
Affinity DataIC50: 85nMAssay Description:Inhibition of recombinant human BuChE using butyrylthiocholine as substrate by Ellman's methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WD44BGPubMed