BDBM50270729 CHEMBL4127367

SMILES [H][C@@]12C[C@@]3([H])[C@@]([H])(CC(=O)[C@@]4([H])C[C@H](CC[C@]34C)O[C@]3([H])O[C@H](CO)[C@@H](O[C@]4([H])O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)[C@H](O)[C@H]3O)[C@]1([H])CC[C@@]1([H])[C@@H](C)[C@]3([H])CC[C@H](C)CN3C[C@@]21[H]

InChI Key InChIKey=PBSTXBXCICGBPQ-QUPYMMALSA-N

Data  2 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 2 hits for monomerid = 50270729   

TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))
Tianjin University Of Technology

Curated by ChEMBL
LigandPNGBDBM50270729(CHEMBL4127367)
Affinity DataIC50:  9.88E+3nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 15 mins followed by substrate addition measured for 30 m...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Tianjin University Of Technology

Curated by ChEMBL
LigandPNGBDBM50270729(CHEMBL4127367)
Affinity DataIC50:  5.71E+3nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate preincubated for 15 mins followed by substrate addition measured for 30 ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed