BDBM50630588 CHEMBL5432192

SMILES CC(C)Cn1cc(C(NS(=O)(=O)C2CC2)C(F)(F)F)c2ccc(cc12)-c1ccccc1C(F)(F)F

InChI Key InChIKey=NECDAWXLCJDWTH-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 = 50630588   

TargetNuclear receptor subfamily 1 group D member 1(Human)
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50630588(CHEMBL5432192)
Affinity DataEC50:  110nMAssay Description:Agonist activity at his6-tagged human REV-ERBalpha LBD (281 to 614 residues) expressed in Escherichia coli assessed as increase in SMRT corepressor p...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/20/2024
Entry Details
PubMed
TargetNuclear receptor subfamily 1 group D member 1(Human)
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50630588(CHEMBL5432192)
Affinity DataEC50:  500nMAssay Description:Agonist activity at REV-ERBalpha LBD in HEK293 cells co-transfected with pG5-UAS pCMV-Gal4 incubated for 18 hrs by multimode plate reader analysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/20/2024
Entry Details
PubMed