BDBM50532733 CHEMBL4556552

SMILES COc1ccc(CN2CCCC(COc3ccc4c(C)c(C)c(=O)oc4c3)C2)cc1OC

InChI Key InChIKey=KLZPNESZOSTZAJ-UHFFFAOYSA-N

Data  8 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 8 hits for monomerid = 50532733   

TargetAmine oxidase [flavin-containing] A(Human)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50532733(CHEMBL4556552)
Affinity DataIC50: 1.72E+3nMAssay Description:Inhibition of human recombinant MAOA expressed in microsomes of baculovirus-infected insect cell using kynuramine as substrate preincubated for 20 mi...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAmine oxidase [flavin-containing] B(Human)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50532733(CHEMBL4556552)
Affinity DataIC50: 90nMAssay Description:Inhibition of human recombinant MAOB expressed in microsomes of baculovirus-infected insect cell using kynuramine as substrate preincubated for 20 mi...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAmine oxidase [flavin-containing] A(Human)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50532733(CHEMBL4556552)
Affinity DataIC50: 1.72E+3nMAssay Description:Inhibition of human recombinant MAOA expressed in microsomes of baculovirus-infected insect cell using kynuramine as substrate preincubated for 20 mi...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAmine oxidase [flavin-containing] B(Human)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50532733(CHEMBL4556552)
Affinity DataIC50: 90nMAssay Description:Inhibition of human recombinant MAOB expressed in microsomes of baculovirus-infected insect cell using kynuramine as substrate preincubated for 20 mi...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCholinesterase(Horse)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50532733(CHEMBL4556552)
Affinity DataIC50: 6.04E+3nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate preincubated for 20 mins followed by substrate addition measured for 5 m...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAcetylcholinesterase(Electric eel)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50532733(CHEMBL4556552)
Affinity DataIC50: 2.21E+3nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 20 mins followed by substrate addition measured for 5 mi...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCholinesterase(Horse)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50532733(CHEMBL4556552)
Affinity DataIC50: 6.04E+3nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate preincubated for 20 mins followed by substrate addition measured for 5 m...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAcetylcholinesterase(Electric eel)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50532733(CHEMBL4556552)
Affinity DataIC50: 2.21E+3nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 20 mins followed by substrate addition measured for 5 mi...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed