BDBM50316369 3-(2-N-Piperidyl-acetamino)-7,8-dehydrorutaecarpine::CHEMBL1098308

SMILES O=C(CN1CCCCC1)Nc1ccc2nc3c4[nH]c5ccccc5c4ccn3c(=O)c2c1

InChI Key InChIKey=WLAAJJZNAFKAMK-UHFFFAOYSA-N

Data  6 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 6 hits for monomerid = 50316369   

TargetAcetylcholinesterase(Electric eel)
Sun Yat-Sen University

Curated by ChEMBL
LigandPNGBDBM50316369(3-(2-N-Piperidyl-acetamino)-7,8-dehydrorutaecarpin...)
Affinity DataIC50: 10.1nMAssay Description:inhibition of electric eel AChE by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/19/2010
Entry Details Article
PubMed
TargetCholinesterase(Horse)
Sun Yat-Sen University

Curated by ChEMBL
LigandPNGBDBM50316369(3-(2-N-Piperidyl-acetamino)-7,8-dehydrorutaecarpin...)
Affinity DataIC50: 5.43E+3nMAssay Description:inhibition of equine serum BuChE by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/19/2010
Entry Details Article
PubMed
TargetCholinesterase(Horse)
Sun Yat-Sen University

Curated by ChEMBL
LigandPNGBDBM50316369(3-(2-N-Piperidyl-acetamino)-7,8-dehydrorutaecarpin...)
Affinity DataIC50: 2.32E+4nMAssay Description:Inhibition of horse serum butyrylcholinesterase using butylthiocholine as substrate incubated for 15 mins followed by substrate addition measured for...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/12/2014
Entry Details Article
PubMed
TargetAcetylcholinesterase(Electric eel)
Sun Yat-Sen University

Curated by ChEMBL
LigandPNGBDBM50316369(3-(2-N-Piperidyl-acetamino)-7,8-dehydrorutaecarpin...)
Affinity DataIC50: 70nMAssay Description:Inhibition of electric eel acetylcholinesterase using acetylthiocholine as substrate incubated for 15 mins followed by substrate addition measured fo...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/12/2014
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Univ. Grenoble Alpes

Curated by ChEMBL
LigandPNGBDBM50316369(3-(2-N-Piperidyl-acetamino)-7,8-dehydrorutaecarpin...)
Affinity DataIC50: 10nMAssay Description:Inhibition of AChE (unknown origin) using acetylthiocholine iodide as substrate incubated for 20 mins followed by substrate addition by Ellman's meth...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/20/2024
Entry Details
PubMed
TargetCholinesterase(Human)
Univ. Grenoble Alpes

Curated by ChEMBL
LigandPNGBDBM50316369(3-(2-N-Piperidyl-acetamino)-7,8-dehydrorutaecarpin...)
Affinity DataIC50: 5.40E+3nMAssay Description:Inhibition of BuChE (unknown origin) using acetylthiocholine iodide as substrate incubated for 20 mins followed by substrate addition by Ellman's met...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/20/2024
Entry Details
PubMed