null

SMILES Cl.Cl.CC1=CC2CC(C1)c1c(C2)nc2cc(Cl)ccc2c1NCCCCCNC(=O)[C@@H](N)Cc1c[nH]c2ccccc12

InChI Key

  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 = 50571188   

TargetAcetylcholinesterase(Homo sapiens (Human))TBA
LigandPNGBDBM50571188(CHEMBL4874244)copy SMILES
Affinity DataIC50: 23nMAssay 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
LigandPNGBDBM50571188(CHEMBL4874244)copy SMILES
Affinity DataIC50: 2.40E+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
LigandPNGBDBM50571188(CHEMBL4874244)copy SMILES
Affinity DataIC50: 68nMAssay 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