BDBM50163238 4-Pyridin-4-yl-piperazine-1-carboxylic acid (4-chloro-phenyl)-amide::CHEMBL367728

SMILES Clc1ccc(NC(=O)N2CCN(CC2)c2ccncc2)cc1

InChI Key InChIKey=XWOBPSKJNFBNJL-UHFFFAOYSA-N

Data  1 IC50  2 EC50

  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 3 hits for monomerid = 50163238   

TargetTransient receptor potential cation channel subfamily V member 1(Rattus norvegicus (rat))
Johnson & Johnson Pharmaceutical Research And Development

Curated by ChEMBL
LigandPNGBDBM50163238(4-Pyridin-4-yl-piperazine-1-carboxylic acid (4-chl...)
Affinity DataEC50:  3.60E+3nMAssay Description:Effective concentration against rat transient receptor potential vanilloid 1 receptor (n=6)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAspartate aminotransferase, cytoplasmic(Homo sapiens)
California Institute For Biomedical Research

Curated by ChEMBL
LigandPNGBDBM50163238(4-Pyridin-4-yl-piperazine-1-carboxylic acid (4-chl...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of GOT1 (unknown origin) using aspartate and alpha-ketoglutarate as substrate after 20 mins by MDH1 enzyme-coupled fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research And Development

Curated by ChEMBL
LigandPNGBDBM50163238(4-Pyridin-4-yl-piperazine-1-carboxylic acid (4-chl...)
Affinity DataEC50:  7.24E+3nMAssay Description:Effective concentration against human transient receptor potential vanilloid 1 receptor (n=6)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed