BDBM50202469 CHEMBL3906647

SMILES: COc1cc(\C=C\C)cc2[C@@H](C)[C@@H](Oc12)c1cc(OC)c(O)c(OC)c1

InChI Key: InChIKey=LYZVPGMCGPXCQO-FVFSBHJXSA-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 = 50202469   

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))	BDBM50202469 (CHEMBL3906647) Show SMILES COc1cc(\C=C\C)cc2[C@@H](C)[C@@H](Oc12)c1cc(OC)c(O)c(OC)c1 |r| Show InChI InChI=1S/C21H24O5/c1-6-7-13-8-15-12(2)20(26-21(15)18(9-13)25-5)14-10-16(23-3)19(22)17(11-14)24-4/h6-12,20,22H,1-5H3/b7-6+/t12-,20-/m1/s1	Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	n/a	n/a	1.60E+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