null

SMILES CC(=O)N1CCN(CC1)c1ccc(CN(C2CCC2)S(=O)(=O)Cc2cccc(F)c2)c(F)c1

InChI Key InChIKey=FYGAIQJENXBISH-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 3 hits for monomerid = 50090088   

TargetNuclear receptor ROR-gamma(Homo sapiens (Human))
Genentech, Inc.

US Patent
LigandPNGBDBM50090088(CHEMBL3581535 | US9216988, 90)copy SMILEScopy InChI
Affinity DataIC50: 25nMpH: 7.4Assay Description:On day of the assay, 100 uL of 0.05% CHAPS (in deionized H2O) was added to all wells of the GFB Unifilter plate and allowed soak for 1 h. A wash bu...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2TB15QCUS Patent
TargetNuclear receptor ROR-gamma(Homo sapiens (Human))
Genentech, Inc.

US Patent
LigandPNGBDBM50090088(CHEMBL3581535 | US9216988, 90)copy SMILEScopy InChI
Affinity DataEC50:  10nMAssay Description:Inverse agonist activity at N-terminal 6xHis-tagged human RORc ligand binding domain (241 to 486) expressed in bacterial expression system assessed a...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TT4SPBPubMed
TargetNuclear receptor ROR-gamma(Homo sapiens (Human))
Genentech, Inc.

US Patent
LigandPNGBDBM50090088(CHEMBL3581535 | US9216988, 90)copy SMILEScopy InChI
Affinity DataIC50: 25nMAssay Description:Displacement of [3H2]-25-hydroxycholesterol from N-terminal 6xHis-tagged human RORc ligand binding domain (241 to 486) expressed in bacterial express...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TT4SPBPubMed