BDBM50234797 CHEMBL4062429

SMILES [H][C@]1(CC[C@@]2(CC[C@]3(C)[C@]([H])(CC[C@]4([H])[C@@]5(C)CC[C@H](OC(C)=O)C(C)(C)[C@]5([H])CC[C@@]34C)[C@@]12[H])C(=O)OCc1ccccc1)[C@H](C)N

InChI Key InChIKey=OKYHOBSZADFCSF-PRAKDZCNSA-N

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 = 50234797   

TargetCholinesterase(Equus caballus (Horse))
Martin-Luther-University Halle-Wittenberg

Curated by ChEMBL
LigandPNGBDBM50234797(CHEMBL4062429)
Affinity DataKi:  380nMAssay Description:Competitive inhibition of equine serum BChE using butyrylthiocholine iodide as substrate preincubated for 20 mins followed by substrate addition meas...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Martin-Luther-University Halle-Wittenberg

Curated by ChEMBL
LigandPNGBDBM50234797(CHEMBL4062429)
Affinity DataKi:  6.78E+3nMAssay Description:Uncompetitive inhibition of equine serum BChE using butyrylthiocholine iodide as substrate preincubated for 20 mins followed by substrate addition me...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))
Martin-Luther-University Halle-Wittenberg

Curated by ChEMBL
LigandPNGBDBM50234797(CHEMBL4062429)
Affinity DataKi:  1.07E+4nMAssay Description:Competitive inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 20 mins followed by substrate addition measu...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))
Martin-Luther-University Halle-Wittenberg

Curated by ChEMBL
LigandPNGBDBM50234797(CHEMBL4062429)
Affinity DataKi:  3.42E+4nMAssay Description:Uncompetitive inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 20 mins followed by substrate addition mea...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed