BDBM50505376 CHEMBL4461328

SMILES CCCCCCC1=C([C@@]2(CC[C@@H]([C@@H]2C1)OS(=O)(=O)N)C(=C)c3ccccc3)c4ccccc4

InChI Key InChIKey=TUITYPXKFZGOFR-UHFFFAOYSA-N

Data  2 EC50

PDB links: 1 PDB ID matches this monomer.

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50505376   

TargetNuclear receptor subfamily 5 group A member 2(Human)
Emory University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50505376(CHEMBL4461328)
Affinity DataEC50:  900nMAssay Description:Agonist activity at human full length LRH1 transfected in human HeLa cells incubated for 24 hrs by renilla luciferase reporter gene assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
2/18/2021
Entry Details Article
PubMedPDB3D3D Structure (crystal)
TargetNuclear receptor subfamily 5 group A member 2(Human)
Emory University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50505376(CHEMBL4461328)
Affinity DataEC50:  600nMAssay Description:Agonist activity at recombinant human LRH1 ligand binding domain (300 to 537 residues) expressed in Escherichia coli BL21 cells assessed as increase ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/18/2021
Entry Details Article
PubMedPDB3D3D Structure (crystal)