BDBM50662166 CHEMBL6168694

SMILES NC1CCN(c2ccc(NC3=C(c4ccccc4)C(=O)N(Cc4ccccc4)C3=O)cc2)CC1

InChI Key InChIKey=DETJIEYUMKAIAQ-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 = 50662166   

TargetOxysterols receptor LXR-beta(Human)
University of Tuebingen

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50662166BDBM50662166(CHEMBL6168694)
Affinity DataEC50:  120nMAssay Description:Agonist activity at GST-tagged LXRbeta LBD (unknown origin) measured after 6 hrs in presence of fluorescein-TRAP220/DRIP-2 by TR-FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
6/5/2026
Entry Details
PubMed
TargetOxysterols receptor LXR-alpha(Human)
University of Tuebingen

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50662166BDBM50662166(CHEMBL6168694)
Affinity DataEC50:  630nMAssay Description:Agonist activity at GST-tagged LXRalpha LBD (unknown origin) measured after 6 hrs in presence of fluorescein-TRAP220/DRIP-2 by TR-FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
6/5/2026
Entry Details
PubMed
TargetOxysterols receptor LXR-alpha(Human)
University of Tuebingen

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50662166BDBM50662166(CHEMBL6168694)
Affinity DataEC50:  1.48E+3nMAssay Description:Agonist activity at LXRalpha (unknown origin) transfected in NR1H2 knockout human Hep3B cells co-transfected with LXRE-GFP measured after 48 hrs by L...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
6/5/2026
Entry Details
PubMed