BDBM50557793 CHEMBL4744735

SMILES CCCC(=O)Nc1ccc(Oc2ccc(Cl)c3ccccc23)c(Cl)c1

InChI Key InChIKey=JMDQFVFDWAYBOU-UHFFFAOYSA-N

Data  1 IC50  2 EC50

  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 3 hits for monomerid = 50557793   

TargetSteroid hormone receptor ERR1(Human)
Daiichi Sankyo

Curated by ChEMBL
LigandPNGBDBM50557793(CHEMBL4744735)
Affinity DataIC50: 350nMAssay Description:Inhibition of FITC-RIP140 peptide binding to N-terminal His-tagged human GST-ERRalpha-LBD (290 to 519 residues) expressed in Escherichia coli incubat...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/26/2022
Entry Details Article
PubMed
TargetSteroid hormone receptor ERR1(Human)
Daiichi Sankyo

Curated by ChEMBL
LigandPNGBDBM50557793(CHEMBL4744735)
Affinity DataEC50: >1.00E+4nMAssay Description:Agonist activity at recombinant full-length human ERRalpha expressed in MG63 cells assessed as transcriptional activation incubated for 18 hrs by dua...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/26/2022
Entry Details Article
PubMed
TargetPeroxisome proliferator-activated receptor gamma(Human)
Daiichi Sankyo

Curated by ChEMBL
LigandPNGBDBM50557793(CHEMBL4744735)
Affinity DataEC50: >1.00E+4nMAssay Description:Agonist activity at full-length PPARgamma (unknown origin) expressed in MG63 cells assessed as transcriptional activation incubated for 18 hrs by dua...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/26/2022
Entry Details Article
PubMed