BDBM50016980 6-(4-(3,4-dimethoxybenzoyl)piperazin-1-yl)-3,4-dihydroquinolin-2(1H)-one::6-[4-(3,4-Dimethoxy-benzoyl)-piperazin-1-yl]-3,4-dihydro-1H-quinolin-2-one::6-[4-(3,4-Dimethoxy-benzoyl)-piperazin-1-yl]-3,4-dihydro-1H-quinolin-2-one(OPC-8212)::CHEMBL17423::VESNARINONE::[4-(3,4-Dihydro-quinolin-6-yl)-piperazin-1-yl]-(3,4-dimethoxy-phenyl)-methanone

SMILES COc1ccc(cc1OC)C(=O)N1CCN(CC1)c1ccc2NC(=O)CCc2c1

InChI Key InChIKey=ZVNYJIZDIRKMBF-UHFFFAOYSA-N

Data  9 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 9 hits for monomerid = 50016980   

TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Tcg Lifesciences

Curated by ChEMBL
LigandPNGBDBM50016980(6-(4-(3,4-dimethoxybenzoyl)piperazin-1-yl)-3,4-dih...)
Affinity DataIC50:  1.10E+3nMAssay Description:Inhibition of human ERGMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetcGMP-inhibited 3',5'-cyclic phosphodiesterase 3A(Homo sapiens (Human))
Daqing Oil Field General Hospital

Curated by ChEMBL
LigandPNGBDBM50016980(6-(4-(3,4-dimethoxybenzoyl)piperazin-1-yl)-3,4-dih...)
Affinity DataIC50:  1.12E+4nMAssay Description:Inhibition of human PDE3A using FAM-cAMP by fluorescence polarization assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetcGMP-inhibited 3',5'-cyclic phosphodiesterase 3B(Homo sapiens (Human))
Daqing Oil Field General Hospital

Curated by ChEMBL
LigandPNGBDBM50016980(6-(4-(3,4-dimethoxybenzoyl)piperazin-1-yl)-3,4-dih...)
Affinity DataIC50:  1.45E+4nMAssay Description:Inhibition of human PDE3B using FAM-cAMP by fluorescence polarization assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Tcg Lifesciences

Curated by ChEMBL
LigandPNGBDBM50016980(6-(4-(3,4-dimethoxybenzoyl)piperazin-1-yl)-3,4-dih...)
Affinity DataIC50:  1.10E+3nMAssay Description:Inhibition of human Potassium channel HERG expressed in mammalian cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetcGMP-inhibited 3',5'-cyclic phosphodiesterase 3A/3B(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50016980(6-(4-(3,4-dimethoxybenzoyl)piperazin-1-yl)-3,4-dih...)
Affinity DataIC50:  6.20E+3nMAssay Description:In vivo inhibition of cyclic AMP phosphodiesterase from human plateletsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetcGMP-inhibited 3',5'-cyclic phosphodiesterase 3A(Homo sapiens (Human))
Daqing Oil Field General Hospital

Curated by ChEMBL
LigandPNGBDBM50016980(6-(4-(3,4-dimethoxybenzoyl)piperazin-1-yl)-3,4-dih...)
Affinity DataIC50:  1.07E+4nMAssay Description:Inhibition of human PDE3A by fluorescence microplate readerMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetcGMP-inhibited 3',5'-cyclic phosphodiesterase 3B(Homo sapiens (Human))
Daqing Oil Field General Hospital

Curated by ChEMBL
LigandPNGBDBM50016980(6-(4-(3,4-dimethoxybenzoyl)piperazin-1-yl)-3,4-dih...)
Affinity DataIC50:  1.32E+4nMAssay Description:Inhibition of human PDE3B by fluorescence microplate readerMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Tcg Lifesciences

Curated by ChEMBL
LigandPNGBDBM50016980(6-(4-(3,4-dimethoxybenzoyl)piperazin-1-yl)-3,4-dih...)
Affinity DataIC50:  1.10E+3nMAssay Description:Inhibition of human ERG expressed in CHO cells by whole cell patch clamp techniqueMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Tcg Lifesciences

Curated by ChEMBL
LigandPNGBDBM50016980(6-(4-(3,4-dimethoxybenzoyl)piperazin-1-yl)-3,4-dih...)
Affinity DataIC50:  1.80E+4nMAssay Description:Inhibitory concentration against IKr potassium channelMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed