null

SMILES CC(C)c1cccc2c(cc(nc12)-c1ccc([nH]1)-c1ccc(cc1)C(O)=O)-c1ccccc1

InChI Key InChIKey=LSGNKLDHMQVTEK-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 = 50099474   

TargetRetinoic acid receptor alpha(Homo sapiens (Human))
Eisai Co., Ltd.

Curated by ChEMBL
LigandPNGBDBM50099474(4-[5-(8-Isopropyl-4-phenyl-quinolin-2-yl)-1H-pyrro...)copy SMILEScopy InChI
Affinity DataIC50: 31nMAssay Description:Antagonistic activity of the compound was evaluated in terms of inhibition of Retinoic acid receptor alpha transactivation by ATRA (50 nM)More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26M3643PubMed
TargetRetinoic acid receptor beta(Homo sapiens (Human))
Eisai Co., Ltd.

Curated by ChEMBL
LigandPNGBDBM50099474(4-[5-(8-Isopropyl-4-phenyl-quinolin-2-yl)-1H-pyrro...)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+3nMAssay Description:Antagonistic activity of the compound was evaluated in terms of inhibition of Retinoic acid receptor beta transactivation by ATRA (50 nM); Not detect...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26M3643PubMed
TargetRetinoic acid receptor gamma(Homo sapiens (Human))
Eisai Co., Ltd.

Curated by ChEMBL
LigandPNGBDBM50099474(4-[5-(8-Isopropyl-4-phenyl-quinolin-2-yl)-1H-pyrro...)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+3nMAssay Description:Antagonistic activity of the compound was evaluated in terms of inhibition of Retinoic acid receptor gamma transactivation by ATRA (50 nM); Not detec...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26M3643PubMed