BDBM50270723 CHEMBL4127029

SMILES [H][C@@]12C[C@@]3([H])[C@@]([H])(C[C@H](O)[C@@]4([H])C[C@H](CC[C@]34C)O[C@]3([H])O[C@H](CO)[C@@H](O)[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=RRZZOQYXEGRKNH-UHFFFAOYSA-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 = 50270723   

TargetAcetylcholinesterase(Electric eel)
Tianjin University of Technology

Curated by ChEMBL
LigandPNGBDBM50270723(CHEMBL4127029)
Affinity DataIC50: 5.15E+4nMAssay 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 Depth
Date in BDB:
4/20/2020
Entry Details Article
PubMed
TargetCholinesterase(Horse)
Tianjin University of Technology

Curated by ChEMBL
LigandPNGBDBM50270723(CHEMBL4127029)
Affinity DataIC50: 1.35E+4nMAssay 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 Depth
Date in BDB:
4/20/2020
Entry Details Article
PubMed