BDBM50202470 CHEMBL3922119

SMILES: COc1ccc(cc1OC)[C@@H](OC(C)=O)[C@H](C)Oc1c(OC)cc(CC=C)cc1OC

InChI Key: InChIKey=SITDJJDXDVFCAP-WNSKOXEYSA-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 = 50202470   

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))	BDBM50202470 (CHEMBL3922119) Show SMILES COc1ccc(cc1OC)[C@@H](OC(C)=O)[C@H](C)Oc1c(OC)cc(CC=C)cc1OC |r| Show InChI InChI=1S/C24H30O7/c1-8-9-17-12-21(28-6)24(22(13-17)29-7)30-15(2)23(31-16(3)25)18-10-11-19(26-4)20(14-18)27-5/h8,10-15,23H,1,9H2,2-7H3/t15-,23-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	n/a	n/a	1.40E+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