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SMILES COc1cc(\C=C\C(=O)NCC(=O)Nc2ccc3[nH]ccc3c2)ccc1O

InChI Key

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50564501   

TargetAcetylcholinesterase(Homo sapiens (Human))TBA
LigandPNGBDBM50564501(CHEMBL4799941)copy SMILES
Affinity DataIC50: 5.74E+3nMAssay Description:Inhibition of recombinant human erythrocyte AChE using acetylthiocholine iodide as substrate preincubated for 30 mins followed by substrate addition ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35ZCBPubMed
TargetCholinesterase(Equus caballus (Horse))TBA
LigandPNGBDBM50564501(CHEMBL4799941)copy SMILES
Affinity DataIC50: 1.41E+4nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate preincubated with enzyme for 30 mins followed by substrate addition and ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28W3J18PubMed
TargetAcetylcholinesterase(Homo sapiens (Human))TBA
LigandPNGBDBM50564501(CHEMBL4799941)copy SMILES
Affinity DataIC50: 5.74E+3nMAssay Description:Inhibition of AChE in human erythrocytes using acetylthiocholine iodide as substrate preincubated with enzyme for 30 mins followed by substrate addit...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28W3J18PubMed
TargetCholinesterase(Equus caballus (Horse))TBA
LigandPNGBDBM50564501(CHEMBL4799941)copy SMILES
Affinity DataIC50: 1.41E+4nMAssay Description:Inhibition of recombinant equine serum BuChE using butyryl thiocholine iodide as substrate preincubated for 30 mins followed by substrate addition an...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35ZCBPubMed