BDBM50467998 CHEMBL4288877

SMILES CCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCCCCCC

InChI Key InChIKey=IJFVSSZAOYLHEE-SSEXGKCCSA-N

Data  2 KI  1 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 3 hits for monomerid = 50467998   

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

Curated by ChEMBL
LigandPNGBDBM50467998(CHEMBL4288877)
Affinity DataKi:  81nMAssay Description:Displacement of 6N-FAM from human LRH1 LBD (299 to 541 residues) expressed in Escherichia coli BL21 pLysS by competitive binding based fluorescence p...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSteroidogenic factor 1(Homo sapiens (Human))
Emory University

Curated by ChEMBL
LigandPNGBDBM50467998(CHEMBL4288877)
Affinity DataKi:  850nMAssay Description:Displacement of 6N-FAM from SF1 LBD (218 to 461 residues) (unknown origin) expressed in Escherichia coli BL21 pLysS by competitive binding based fluo...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNuclear receptor subfamily 5 group A member 2(Homo sapiens (Human))
Emory University

Curated by ChEMBL
LigandPNGBDBM50467998(CHEMBL4288877)
Affinity DataEC50: >1.00E+5nMAssay Description:Agonist activity at recombinant full length human LRH1 expressed in HeLa cells after 24 hrs by dual-glo luciferase reporter gene assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed