BDBM50234789 CHEMBL4063629

SMILES [H][C@]12[C@@H](CC[C@@]1(CC[C@]1(C)[C@]2([H])CC[C@]2([H])[C@@]3(C)CC[C@H](O)C(C)(C)[C@]3([H])CC[C@@]12C)C(=O)OCc1ccccc1)C(C)=O

InChI Key InChIKey=TZPWJFBZFIGPET-KYIMJNNYSA-N

Data  3 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 3 hits for monomerid = 50234789   

TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))
Martin-Luther-University Halle-Wittenberg

Curated by ChEMBL
LigandPNGBDBM50234789(CHEMBL4063629)
Affinity DataKi:  590nMAssay 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
LigandPNGBDBM50234789(CHEMBL4063629)
Affinity DataKi:  4.06E+3nMAssay 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
TargetCholinesterase(Equus caballus (Horse))
Martin-Luther-University Halle-Wittenberg

Curated by ChEMBL
LigandPNGBDBM50234789(CHEMBL4063629)
Affinity DataKi: >1.00E+4nMAssay 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