BDBM50575871 CHEMBL4855847

SMILES OC(=O)CCc1nc(c(o1)-c1cc(cc(c1)C(F)(F)F)C(F)(F)F)-c1ccccc1

InChI Key InChIKey=KMMWBOHSOIDNLP-UHFFFAOYSA-N

Data  3 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 = 50575871   

TargetRetinoic acid receptor RXR-alpha(Human)
Goethe-University Frankfurt

Curated by ChEMBL
LigandPNGBDBM50575871(CHEMBL4855847)
Affinity DataEC50:  50nMAssay Description:Agonist activity at human RXRalpha transfected in human HEK293T cells co-expressing pFR/pRL-Luc incubated for 14 to 16 hrs by hybrid reporter gene as...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetRetinoic acid receptor RXR-beta(Human)
Goethe-University Frankfurt

Curated by ChEMBL
LigandPNGBDBM50575871(CHEMBL4855847)
Affinity DataEC50:  440nMAssay Description:Agonist activity at human RXRbeta transfected in human HEK293T cells co-expressing pFR/pRL-Luc incubated for 14 to 16 hrs by hybrid reporter gene ass...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetRetinoic acid receptor RXR-gamma(Human)
Goethe-University Frankfurt

Curated by ChEMBL
LigandPNGBDBM50575871(CHEMBL4855847)
Affinity DataEC50:  50nMAssay Description:Agonist activity at human RXRgamma transfected in human HEK293T cells co-expressing pFR/pRL-Luc incubated for 14 to 16 hrs by hybrid reporter gene as...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed