null

SMILES CC(C)(C)[Si](C)(C)O[C@H]1C=C2CCN3Cc4cc5OCOc5cc4[C@@H]([C@@H]23)[C@@H]1O

InChI Key InChIKey=RLYPONLPAHPYMG-UWHLTILDSA-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 2 hits for monomerid = 50293600   

TargetCytochrome P450 3A4(Homo sapiens (Human))
McMaster University

Curated by ChEMBL
LigandPNGBDBM50293600((1S,2S,3a1S,12bS)-2-(tert-butyldimethylsilyloxy)-2...)copy SMILEScopy InChI
Affinity DataKi:  260nMAssay Description:Inhibition of human CYP3A4 assessed as biotransformation of 7-benzyloxyquinolineMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2X92BBGPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
McMaster University

Curated by ChEMBL
LigandPNGBDBM50293600((1S,2S,3a1S,12bS)-2-(tert-butyldimethylsilyloxy)-2...)copy SMILEScopy InChI
Affinity DataKi:  860nMAssay Description:Inhibition of AChE by Ellman's assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CN7437PubMed