BDBM132072 US8841453, 2

SMILES CC(=O)NCCc1c[nH]c2ccc(OC(=O)NCCNc3c4CCCCc4nc4ccccc34)cc12

InChI Key InChIKey=WSXAJVAWKDKQHT-UHFFFAOYSA-N

Data  4 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 132072   

TargetAcetylcholinesterase(Homo sapiens (Human))
Uniwersytet Warszawski

US Patent
LigandPNGBDBM132072(US8841453, 2)
Affinity DataIC50:  1.10E+3nMAssay Description:The biological activity of the compounds of general formula (I) towards the cholinesterase inhibition was evaluated using Ellman's method (Ellman, G....More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetCholinesterase(Homo sapiens (Human))
Csir-Central Drug Research Institute

Curated by ChEMBL
LigandPNGBDBM132072(US8841453, 2)
Affinity DataIC50:  4.30nMAssay Description:Inhibition of human plasma butyrylcholinesterase using butyrylthiocholine as substrate preincubated for 30 mins followed by substrate addition and me...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Uniwersytet Warszawski

US Patent
LigandPNGBDBM132072(US8841453, 2)
Affinity DataIC50:  1.10E+3nMAssay Description:Inhibition of human erythrocyte acetylcholinesterase using acetylthiocholine as substrate preincubated for 30 mins followed by substrate addition and...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Homo sapiens (Human))
Csir-Central Drug Research Institute

Curated by ChEMBL
LigandPNGBDBM132072(US8841453, 2)
Affinity DataIC50:  4.28nMAssay Description:The biological activity of the compounds of general formula (I) towards the cholinesterase inhibition was evaluated using Ellman's method (Ellman, G....More data for this Ligand-Target Pair
In DepthDetails US Patent