BDBM50388639 CHEMBL2059558

SMILES: [O-][N+](=O)c1ccc(CN(CC2COc3ccccc3O2)Cc2ccc(Cl)cc2)s1

InChI Key: InChIKey=CZVVVMJVSLOVTG-UHFFFAOYSA-N

Data: 1 EC50

Find this compound or compounds like it in BindingDB or PDB:

Substructure Similarity at least:  must be >=0.5 Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50388639   

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
Nuclear receptor subfamily 1 group D member 1 (Homo sapiens (Human))	BDBM50388639 (CHEMBL2059558) Show SMILES [O-][N+](=O)c1ccc(CN(CC2COc3ccccc3O2)Cc2ccc(Cl)cc2)s1 Show InChI InChI=1S/C21H19ClN2O4S/c22-16-7-5-15(6-8-16)11-23(13-18-9-10-21(29-18)24(25)26)12-17-14-27-19-3-1-2-4-20(19)28-17/h1-10,17H,11-14H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	n/a	n/a	7.80E+3	n/a	n/a	n/a	n/a
The Scripps Research Institute Curated by ChEMBL					Assay Description Agonist activity at Rev-Erbalpha expressed in HEK293 cells coexpressing BamII promoter assessed as repression of transcription after 24 hrs by dual-G...				Bioorg Med Chem Lett 22: 4413-7 (2012) Article DOI: 10.1016/j.bmcl.2012.04.126 BindingDB Entry DOI: 10.7270/Q2D21ZPZ
					More data for this Ligand-Target Pair