BDBM50393715 CHEMBL2158994

SMILES CN(C)CCOc1ccc(cc1)C(=O)\C=C\c1ccccc1

InChI Key InChIKey=AAJCCATVSUSRCY-MDWZMJQESA-N

Data  2 KI  3 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 5 hits for monomerid = 50393715   

TargetAcetylcholinesterase(Homo sapiens (Human))
Hu'Nan University

Curated by ChEMBL
LigandPNGBDBM50393715(CHEMBL2158994)
Affinity DataKi:  3.52E+3nMAssay Description:Non-competitive inhibition of AChE (unknown origin) incubated for 25 mins by Lineweaver-Burk plot analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Hu'Nan University

Curated by ChEMBL
LigandPNGBDBM50393715(CHEMBL2158994)
Affinity DataKi:  7.99E+3nMAssay Description:Competitive inhibition of AChE (unknown origin) incubated for 25 mins by Lineweaver-Burk plot analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Hu'Nan University

Curated by ChEMBL
LigandPNGBDBM50393715(CHEMBL2158994)
Affinity DataIC50:  4.68E+3nMAssay Description:Inhibition of AChE (unknown origin) using acetylthiocholine iodide as substrate incubated for 25 mins by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetQuinolone resistance protein NorA(Staphylococcus aureus)
University Of Copenhagen

Curated by ChEMBL
LigandPNGBDBM50393715(CHEMBL2158994)
Affinity DataIC50:  2.84E+4nMAssay Description:Inhibition of norA-mediated ethidium bromide efflux in methicillin-resistant Staphylococcus aureus SA-1199B by spectrofluorometric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Homo sapiens (Human))
Hu'Nan University

Curated by ChEMBL
LigandPNGBDBM50393715(CHEMBL2158994)
Affinity DataIC50:  2.04E+4nMAssay Description:Inhibition of BuChE (unknown origin) using butyrylthiocholine iodide as substrate incubated for 25 mins by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed