null

SMILES [H][C@@]12[#6][C@@]3([#6]\[#6]=[#6](\[#6])-[#6])[#6](=O)C4([#6]-[#6@H](-[#6](-[#6])-[#6])C([#6])([#6])[#6@H](-[#8])[C@@]14[H])[#6](=O)[C@]([#6](=O)-c1ccccc1)([#6]3=O)C2([#6])[#6]

InChI Key InChIKey=NUZKNNSXCUXINE-CQSZACIVSA-N

  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 1 hit for monomerid = 50090183   

TargetAcetylcholinesterase(Homo sapiens (Human))
Chinese Academy of Sciences

Curated by ChEMBL
LigandPNGBDBM50090183(CHEMBL3581576)copy SMILEScopy InChI
Affinity DataIC50: 2.64E+4nMAssay Description:Inhibition of human erythrocytes acetylcholinesterase after 30 mins using S-acetylthiocholine iodide substrate by spectrophotometry based Ellman meth...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FJ2JH8PubMed