BDBM50016845 HEXAFLUORENIUM BROMIDE::Hexaflurone Bromide::Hexafluronium Bromide::Mylaxen

SMILES [Br-].[Br-].C[N+](C)(CCCCCC[N+](C)(C)C1c2ccccc2-c2ccccc12)C1c2ccccc2-c2ccccc12

InChI Key InChIKey=WDEFPRUEZRUYNW-UHFFFAOYSA-L

Data  4 KI

  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 = 50016845   

TargetCarboxylic ester hydrolase(Equus caballus (Horse))
TBA

Curated by ChEMBL
LigandPNGBDBM50016845(HEXAFLUORENIUM BROMIDE | Hexaflurone Bromide | Hex...)
Affinity DataKi:  340nMAssay Description:Reversible mixed-type inhibition of horse serum butyrylcholinesterase using acetylcholine bromide as substrate assessed as free enzyme-inhibitor comp...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarboxylic ester hydrolase(Equus caballus (Horse))
TBA

Curated by ChEMBL
LigandPNGBDBM50016845(HEXAFLUORENIUM BROMIDE | Hexaflurone Bromide | Hex...)
Affinity DataKi:  890nMAssay Description:Reversible mixed-type inhibition of horse serum butyrylcholinesterase using acetylcholine bromide as substrate by Lineweaver-Burk plot analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))
TBA

Curated by ChEMBL
LigandPNGBDBM50016845(HEXAFLUORENIUM BROMIDE | Hexaflurone Bromide | Hex...)
Affinity DataKi:  1.30E+3nMAssay Description:Reversible mixed-type inhibition of electric eel acetylcholinesterase using acetylcholine bromide as substrate assessed as free enzyme-inhibitor comp...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))
TBA

Curated by ChEMBL
LigandPNGBDBM50016845(HEXAFLUORENIUM BROMIDE | Hexaflurone Bromide | Hex...)
Affinity DataKi:  1.30E+3nMAssay Description:Reversible mixed-type inhibition of electric eel acetylcholinesterase using acetylcholine bromide as substrate by Lineweaver-Burk plot analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed