BDBM50202471 CHEMBL3949874

SMILES: COc1cc(cc(OC)c1O)[C@H](O)[C@@H](C)Oc1c(OC)cc(CC=C)cc1OC

InChI Key: InChIKey=JJVOBQHHQSQIMW-ZUOKHONESA-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 = 50202471   

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
C-C chemokine receptor type 3 (Homo sapiens (Human))	BDBM50202471 (CHEMBL3949874) Show SMILES COc1cc(cc(OC)c1O)[C@H](O)[C@@H](C)Oc1c(OC)cc(CC=C)cc1OC |r| Show InChI InChI=1S/C22H28O7/c1-7-8-14-9-18(27-5)22(19(10-14)28-6)29-13(2)20(23)15-11-16(25-3)21(24)17(12-15)26-4/h7,9-13,20,23-24H,1,8H2,2-6H3/t13-,20-/m1/s1	Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	1.50E+3	n/a	n/a	n/a	n/a
Kindai University Curated by ChEMBL					Assay Description Antagonist activity at human EGFP-fused CCR3 expressed in mouse L1.2 cells assessed as inhibition of CCL11-induced chemotaxis measured after 1.5 hrs ...				J Nat Prod 79: 2005-13 (2016) Article DOI: 10.1021/acs.jnatprod.6b00262 BindingDB Entry DOI: 10.7270/Q2MW2K39
					More data for this Ligand-Target Pair