BDBM19121 N-[(6S,7S,8R,11S,12S,14R,15S,16R)-14-hydroxy-7-(hydroxymethyl)-7,12,16-trimethyl-15-[(1S)-1-(methylamino)ethyl]-18-oxopentacyclo[9.7.0.0^{1,3}.0^{3,8}.0^{12,16}]octadecan-6-yl]-2-methylpropanamide::demethylated N-3-isobutyrylcycloxobuxidine-F, 18

SMILES [H][C@@]12CC[C@]3([H])[C@]4(C[C@@]14C(=O)C[C@]1(C)[C@@H]([C@H](C)NC)[C@H](O)C[C@@]21C)CC[C@H](NC(=O)C(C)C)[C@@]3(C)CO

InChI Key InChIKey=YFRKHWOYCOLFQE-LAYXPMECSA-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 = 19121   

TargetCholinesterase(Homo sapiens (Human))
Cnrs

LigandPNGBDBM19121(N-[(6S,7S,8R,11S,12S,14R,15S,16R)-14-hydroxy-7-(hy...)
Affinity DataIC50:  1.44E+3nMAssay Description:Inhibition of BuChE activity was determined by the spectroscopic method of Ellman using butyrylthiocholine iodide as substrate, in 96-well microtiter...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))
Cnrs

LigandPNGBDBM19121(N-[(6S,7S,8R,11S,12S,14R,15S,16R)-14-hydroxy-7-(hy...)
Affinity DataIC50:  110nMAssay Description:Inhibition of AChE activity was determined by the spectroscopic method of Ellman using acetylthiocholine iodide as substrate, in 96-well microtiter p...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed