null

SMILES O=C1N(Cc2ccccc2)C(=O)C(=C1Nc1ccccc1)c1ccccc1

InChI Key InChIKey=GLDDBILAEOMQJI-UHFFFAOYSA-N

PDB links: 1 PDB ID contains this monomer as substructures. 1 PDB ID contains inhibitors having a similarity of 90% to this monomer.

  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 = 20157   

TargetOxysterols receptor LXR-beta(Homo sapiens (Human))
GlaxoSmithKline

LigandPNGBDBM20157(1-benzyl-3-phenyl-4-(phenylamino)-2,5-dihydro-1H-p...)copy SMILEScopy InChI
Affinity DataEC50:  70nMpH: 7.5 T: 2°CAssay Description:The LXR LiSA measures the ligand-dependent recruitment of a 25 amino acid fragment of the steroid receptor coactivator 1 (SRC1) to the ligand-binding...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26T0JXGPubMed
TargetOxysterols receptor LXR-alpha(Homo sapiens (Human))
GlaxoSmithKline

LigandPNGBDBM20157(1-benzyl-3-phenyl-4-(phenylamino)-2,5-dihydro-1H-p...)copy SMILEScopy InChI
Affinity DataEC50:  100nMpH: 7.5 T: 2°CAssay Description:The LXR LiSA measures the ligand-dependent recruitment of a 25 amino acid fragment of the steroid receptor coactivator 1 (SRC1) to the ligand-binding...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26T0JXGPubMed