BDBM22385 (3aS,6aR)-5-hexyl-N,4-diphenyl-1,2,3,3a,6,6a-hexahydropentalen-3a-amine::bicyclo[3.3.0]-oct-2-ene, 5m

SMILES [H][C@]12CCC[C@@]1(Nc1ccccc1)C(=C(CCCCCC)C2)c1ccccc1

InChI Key InChIKey=ZYOSSUMBVGPRRB-BVAGGSTKSA-N

Data  4 EC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 22385   

TargetNuclear receptor subfamily 5 group A member 2(Homo sapiens (Human))
University Of Southampton

Curated by ChEMBL
LigandPNGBDBM22385((3aS,6aR)-5-hexyl-N,4-diphenyl-1,2,3,3a,6,6a-hexah...)
Affinity DataEC50:  31.6nMAssay Description:Agonist activity at human LRH-1 receptor assessed as TIF2 737-757 peptide recruitment by TR-FRET assay relative to controlMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSteroidogenic factor 1(Homo sapiens (Human))
University Of Southampton

LigandPNGBDBM22385((3aS,6aR)-5-hexyl-N,4-diphenyl-1,2,3,3a,6,6a-hexah...)
Affinity DataEC50:  43nMAssay Description:The screen utilizes a ligand mediated co-factor interaction between purified bacterial expressed ligand binding domain of human SF1 and a peptide der...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNuclear receptor subfamily 5 group A member 2(Homo sapiens (Human))
University Of Southampton

Curated by ChEMBL
LigandPNGBDBM22385((3aS,6aR)-5-hexyl-N,4-diphenyl-1,2,3,3a,6,6a-hexah...)
Affinity DataEC50:  34nMpH: 7.5 T: 2°CAssay Description:The screen utilizes a ligand mediated co-factor interaction between purified bacterial expressed ligand binding domain of human LRH1 and a TIF2-deriv...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSteroidogenic factor 1(Homo sapiens (Human))
University Of Southampton

LigandPNGBDBM22385((3aS,6aR)-5-hexyl-N,4-diphenyl-1,2,3,3a,6,6a-hexah...)
Affinity DataEC50:  39.8nMAssay Description:Agonist activity at human SF-1 assessed as DAX1 1-23 peptide recruitment by TR-FRET assay relative to controlMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed