BDBM50509898 CHEMBL4435008

SMILES [H][C@@]1(CC[C@@]2([H])[C@]3([H])CC=C4C[C@@H](O)CC[C@]4(C)[C@@]3([H])CC[C@]12C)[C@H](C)CC(C)C(=O)N(C)CC

InChI Key InChIKey=XDUQLCBKVBHDGT-UHFFFAOYSA-N

Data  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 2 hits for monomerid = 50509898   

TargetOxysterols receptor LXR-beta(Rat)
Niigata University of Pharmacy and Applied Life Sciences

Curated by ChEMBL
LigandPNGBDBM50509898(CHEMBL4435008)
Affinity DataEC50:  3.90E+3nMAssay Description:Transactivation of rat LXRbeta expressed in HEK293FT cells measured after 14 to 18 hrs by dual-luciferase reporter gene assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
2/20/2021
Entry Details Article
PubMed
TargetOxysterols receptor LXR-beta(Rat)
Niigata University of Pharmacy and Applied Life Sciences

Curated by ChEMBL
LigandPNGBDBM50509898(CHEMBL4435008)
Affinity DataEC50:  3.89E+3nMAssay Description:Transactivation of rat LXRbeta expressed in HEK293FT cells measured after 14 to 18 hrs by dual-luciferase reporter gene assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
2/20/2021
Entry Details Article
PubMed