null

SMILES: CCCCCCCCCCOc1ccc(OCC(=O)COc2cccc(OCC(O)=O)c2)cc1

InChI Key: InChIKey=WALVZJTXULUNEF-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50110853   

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
Cytosolic phospholipase A2 beta (Homo sapiens (Human))	BDBM50110853 (CHEMBL29246 | {3-[3-(4-Decyloxy-phenoxy)-2-oxo-pro...) Show SMILES CCCCCCCCCCOc1ccc(OCC(=O)COc2cccc(OCC(O)=O)c2)cc1 Show InChI InChI=1S/C27H36O7/c1-2-3-4-5-6-7-8-9-17-31-23-13-15-24(16-14-23)32-19-22(28)20-33-25-11-10-12-26(18-25)34-21-27(29)30/h10-16,18H,2-9,17,19-21H2,1H3,(H,29,30)	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	200	n/a	n/a	n/a	n/a	n/a	n/a
AstraZeneca R&D Charnwood Curated by ChEMBL					Assay Description Inhibitory activity against cytosolic Phospholipase A2 (PLA2) by soluble assay				J Med Chem 45: 1348-62 (2002) BindingDB Entry DOI: 10.7270/Q2F76BVP
					More data for this Ligand-Target Pair
Cytosolic phospholipase A2 beta (Homo sapiens (Human))	BDBM50110853 (CHEMBL29246 | {3-[3-(4-Decyloxy-phenoxy)-2-oxo-pro...) Show SMILES CCCCCCCCCCOc1ccc(OCC(=O)COc2cccc(OCC(O)=O)c2)cc1 Show InChI InChI=1S/C27H36O7/c1-2-3-4-5-6-7-8-9-17-31-23-13-15-24(16-14-23)32-19-22(28)20-33-25-11-10-12-26(18-25)34-21-27(29)30/h10-16,18H,2-9,17,19-21H2,1H3,(H,29,30)	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	60	n/a	n/a	n/a	n/a	n/a	n/a
AstraZeneca R&D Charnwood Curated by ChEMBL					Assay Description Inhibitory activity against cytosolic Phospholipase A2 (PLA2) by bilayer assay				J Med Chem 45: 1348-62 (2002) BindingDB Entry DOI: 10.7270/Q2F76BVP
					More data for this Ligand-Target Pair