BDBM50383665 CHEMBL2029885

SMILES: CCOC(=O)C1Cc2ccccc2CN1S(=O)(=O)c1cccc2ccccc12

InChI Key: InChIKey=PCRLBWQGZGUXJH-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 = 50383665   

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))	BDBM50383665 (CHEMBL2029885) Show SMILES CCOC(=O)C1Cc2ccccc2CN1S(=O)(=O)c1cccc2ccccc12 Show InChI InChI=1S/C22H21NO4S/c1-2-27-22(24)20-14-17-9-3-4-10-18(17)15-23(20)28(25,26)21-13-7-11-16-8-5-6-12-19(16)21/h3-13,20H,2,14-15H2,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	1.70E+3	n/a	n/a	n/a	n/a
The Scripps Research Institute Curated by ChEMBL					Assay Description Agonist activity at Rev-erbalpha assessed as repression of transcription by luciferase-reporter gene assay				Bioorg Med Chem Lett 22: 3739-42 (2012) Article DOI: 10.1016/j.bmcl.2012.04.023 BindingDB Entry DOI: 10.7270/Q2CN74ZF
					More data for this Ligand-Target Pair