null

SMILES: COC(=O)c1ccc(\C=C(/C)c2ccc3OCC(C)(C)c3c2)cc1

InChI Key: InChIKey=VHXWBUMFZDHHAP-SDNWHVSQSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50066903   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kcal/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Retinoic acid receptor beta (Homo sapiens (Human))	BDBM50066903 (4-[(E)-2-(3,3-Dimethyl-2,3-dihydro-benzofuran-5-yl...) Show SMILES COC(=O)c1ccc(\C=C(/C)c2ccc3OCC(C)(C)c3c2)cc1 Show InChI InChI=1S/C21H22O3/c1-14(11-15-5-7-16(8-6-15)20(22)23-4)17-9-10-19-18(12-17)21(2,3)13-24-19/h5-12H,13H2,1-4H3/b14-11+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	430	n/a	n/a	n/a	n/a
University of Oklahoma Health Sciences Center Curated by ChEMBL					Assay Description Transcriptional activation in CV-1 cells expressing RAR-beta receptor				J Med Chem 41: 3753-7 (1998) Article DOI: 10.1021/jm980308p BindingDB Entry DOI: 10.7270/Q2TB1628
					More data for this Ligand-Target Pair
Retinoic acid receptor gamma (Homo sapiens (Human))	BDBM50066903 (4-[(E)-2-(3,3-Dimethyl-2,3-dihydro-benzofuran-5-yl...) Show SMILES COC(=O)c1ccc(\C=C(/C)c2ccc3OCC(C)(C)c3c2)cc1 Show InChI InChI=1S/C21H22O3/c1-14(11-15-5-7-16(8-6-15)20(22)23-4)17-9-10-19-18(12-17)21(2,3)13-24-19/h5-12H,13H2,1-4H3/b14-11+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	400	n/a	n/a	n/a	n/a
University of Oklahoma Health Sciences Center Curated by ChEMBL					Assay Description Transcriptional activation in CV-1 cells expressing RAR-gamma receptor				J Med Chem 41: 3753-7 (1998) Article DOI: 10.1021/jm980308p BindingDB Entry DOI: 10.7270/Q2TB1628
					More data for this Ligand-Target Pair