BDBM50234803 CHEMBL4099629

SMILES [H][C@]1(CC[C@]2(COC(C)=O)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@@H](C)N

InChI Key InChIKey=MFXQEPNZKMYOJG-VIFUSZNRSA-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 = 50234803   

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

Curated by ChEMBL
LigandPNGBDBM50234803(CHEMBL4099629)
Affinity DataKi:  60nMAssay 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
LigandPNGBDBM50234803(CHEMBL4099629)
Affinity DataKi:  370nMAssay 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
LigandPNGBDBM50234803(CHEMBL4099629)
Affinity DataKi:  4.50E+3nMAssay 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