BDBM50409078 CHEMBL325761

SMILES Cc1c(C)c(=O)oc2cc(OCc3ccc(F)c(F)c3)ccc12

InChI Key InChIKey=OAIPPRYRUKGVPD-UHFFFAOYSA-N

Data  11 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 11 hits for monomerid = 50409078   

TargetAmine oxidase [flavin-containing] B(Rat)
University of Lausanne

Curated by ChEMBL
LigandPNGBDBM50409078(CHEMBL325761)
Affinity DataIC50: 1.10nMAssay Description:Inhibitory activity against monoamine oxidase BMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAmine oxidase [flavin-containing] A(Rat)
University of Lausanne

Curated by ChEMBL
LigandPNGBDBM50409078(CHEMBL325761)
Affinity DataIC50: 123nMAssay Description:Inhibitory activity against monoamine oxidase AMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAmine oxidase [flavin-containing] A(Rat)
University of Lausanne

Curated by ChEMBL
LigandPNGBDBM50409078(CHEMBL325761)
Affinity DataIC50: 123nMAssay Description:Inhibitory effect on monoamine oxidase A, SD on IC50 values < 10%More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAmine oxidase [flavin-containing] B(Rat)
University of Lausanne

Curated by ChEMBL
LigandPNGBDBM50409078(CHEMBL325761)
Affinity DataIC50: 1.15nMAssay Description:Inhibitory effect on Monoamine oxidase B, SD on IC50 values < 10%More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAmine oxidase [flavin-containing] A(Rat)
University of Lausanne

Curated by ChEMBL
LigandPNGBDBM50409078(CHEMBL325761)
Affinity DataIC50: 123nMAssay Description:Inhibition of rat brain mitochondrial MAOA using kynuramine as substrate assessed as decrease in 4-hydroxyquinoline production by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAmine oxidase [flavin-containing] A(Human)
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50409078(CHEMBL325761)
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of recombinant human MAO-A using p-tyramine as substrate assessed as decrease in H2O2 production incubated for 15 mins by fluorimetric met...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAmine oxidase [flavin-containing] B(Human)
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50409078(CHEMBL325761)
Affinity DataIC50: 4.30nMAssay Description:Inhibition of recombinant human MAO-B using p-tyramine as substrate assessed as decrease in H2O2 production incubated for 15 mins by fluorimetric met...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAmine oxidase [flavin-containing] B(Rat)
University of Lausanne

Curated by ChEMBL
LigandPNGBDBM50409078(CHEMBL325761)
Affinity DataIC50: 1nMAssay Description:Inhibition of rat brain mitochondrial MAOB using kynuramine as substrate assessed as decrease in 4-hydroxyquinoline production by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAmine oxidase [flavin-containing] B(Human)
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50409078(CHEMBL325761)
Affinity DataIC50: 1.10nMAssay Description:Inhibition of MAO-B (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAmine oxidase [flavin-containing] B(Rat)
University of Lausanne

Curated by ChEMBL
LigandPNGBDBM50409078(CHEMBL325761)
Affinity DataIC50: 1.10nMAssay Description:Competitive inhibition of rat brain MAO-BMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAcetylcholinesterase(Human)
Babu Banarasi Das Northern India Institute of Technology

Curated by ChEMBL
LigandPNGBDBM50409078(CHEMBL325761)
Affinity DataIC50: 3.00E+3nMAssay Description:Inhibition of AChE (unknown origin) using acetylthiocholine chloride as substrate incubated for 5 mins by DTNB reagent based Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails
PubMed