BDBM50212166 7-chloro-6H-chromeno[4,3-b]quinoline-3,9-diol::CHEMBL402491

SMILES: Oc1ccc-2c(OCc3c(Cl)c4cc(O)ccc4nc-23)c1

InChI Key: InChIKey=RYBHKLZSHRZGQK-UHFFFAOYSA-N

Data: 2 IC50

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 2 hits for monomerid = 50212166   

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
Estrogen-related receptor alpha (Homo sapiens (Human))	BDBM50212166 (7-chloro-6H-chromeno[4,3-b]quinoline-3,9-diol | CH...) Show SMILES Oc1ccc-2c(OCc3c(Cl)c4cc(O)ccc4nc-23)c1 Show InChI InChI=1S/C16H10ClNO3/c17-15-11-5-8(19)2-4-13(11)18-16-10-3-1-9(20)6-14(10)21-7-12(15)16/h1-6,19-20H,7H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	3.30	n/a	n/a	n/a	n/a	n/a	n/a
Wyeth Research Curated by ChEMBL					Assay Description Inhibition of human ERalpha				Bioorg Med Chem Lett 17: 4053-6 (2007) Article DOI: 10.1016/j.bmcl.2007.04.068 BindingDB Entry DOI: 10.7270/Q2V124HV
					More data for this Ligand-Target Pair
Estrogen-related receptor beta (Homo sapiens (Human))	BDBM50212166 (7-chloro-6H-chromeno[4,3-b]quinoline-3,9-diol | CH...) Show SMILES Oc1ccc-2c(OCc3c(Cl)c4cc(O)ccc4nc-23)c1 Show InChI InChI=1S/C16H10ClNO3/c17-15-11-5-8(19)2-4-13(11)18-16-10-3-1-9(20)6-14(10)21-7-12(15)16/h1-6,19-20H,7H2	PDB MMDB Reactome pathway KEGG B.MOAD GoogleScholar	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	88	n/a	n/a	n/a	n/a	n/a	n/a
Wyeth Research Curated by ChEMBL					Assay Description Inhibition of human ERbeta				Bioorg Med Chem Lett 17: 4053-6 (2007) Article DOI: 10.1016/j.bmcl.2007.04.068 BindingDB Entry DOI: 10.7270/Q2V124HV
					More data for this Ligand-Target Pair