null

SMILES CCN(C(COCC(=O)N(C)C)c1ccccc1)c1ccc(cc1)C(O)(C(F)(F)F)C(F)(F)F

InChI Key InChIKey=HSXPHPZTVBAFKE-UHFFFAOYSA-N

  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 4 hits for monomerid = 50192114   

TargetOxysterols receptor LXR-beta(Homo sapiens (Human))
F. Hoffmann-La Roche Ltd.

Curated by ChEMBL
LigandPNGBDBM50192114(2-(2-(ethyl(4-(1,1,1,3,3,3-hexafluoro-2-hydroxypro...)copy SMILEScopy InChI
Affinity DataIC50: 500nMAssay Description:Binding affinity to LXRbeta by radioligand displacement assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HD7V80PubMed
TargetOxysterols receptor LXR-alpha(Homo sapiens (Human))
F. Hoffmann-La Roche Ltd.

Curated by ChEMBL
LigandPNGBDBM50192114(2-(2-(ethyl(4-(1,1,1,3,3,3-hexafluoro-2-hydroxypro...)copy SMILEScopy InChI
Affinity DataEC50:  800nMAssay Description:Transactivation of LXRalpha by luciferase reporter gene assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HD7V80PubMed
TargetOxysterols receptor LXR-beta(Homo sapiens (Human))
F. Hoffmann-La Roche Ltd.

Curated by ChEMBL
LigandPNGBDBM50192114(2-(2-(ethyl(4-(1,1,1,3,3,3-hexafluoro-2-hydroxypro...)copy SMILEScopy InChI
Affinity DataEC50:  260nMAssay Description:Transactivation of LXRbeta by luciferase reporter gene assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HD7V80PubMed
TargetOxysterols receptor LXR-alpha(Homo sapiens (Human))
F. Hoffmann-La Roche Ltd.

Curated by ChEMBL
LigandPNGBDBM50192114(2-(2-(ethyl(4-(1,1,1,3,3,3-hexafluoro-2-hydroxypro...)copy SMILEScopy InChI
Affinity DataIC50: 900nMAssay Description:Binding affinity to LXRalpha by radioligand displacement assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HD7V80PubMed