BDBM50629933 CHEMBL5395293

SMILES [H][C@]1([#6]-[#6@H](-[#8]-[#6@H]1-[#8])\[#6]=[#6](\[#6])-[#6])[C@]1([H])[#6]-[#6][C@]2([#6])[#6]3=[#6]-[#6][C@@]4([H])C([#6])([#6])[#6](=O)-[#6]-[#6][C@]4([#6])[C@@]3([H])[#6]-[#6][C@@]12[#6]

InChI Key InChIKey=IWMWEOZCYSZLPR-UHFFFAOYSA-N

Data  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 2 hits for monomerid = 50629933   

TargetOxysterols receptor LXR-alpha(Human)
University of Vienna

Curated by ChEMBL
LigandPNGBDBM50629933(CHEMBL5395293)
Affinity DataEC50:  1.60E+3nMAssay Description:Agonist activity at full length human LXRalpha transfected in HEK293T cells co-expressing ABCA1 assessed as increase in luciferase activity measured ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/20/2024
Entry Details
PubMed
TargetOxysterols receptor LXR-beta(Human)
University of Vienna

Curated by ChEMBL
LigandPNGBDBM50629933(CHEMBL5395293)
Affinity DataEC50:  5.30E+3nMAssay Description:Agonist activity at full length human LXRbeta transfected in HEK293T cells co-expressing ABCA1 assessed as increase in luciferase activity measured a...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/20/2024
Entry Details
PubMed