null

SMILES: COc1cc(\C=C\C(=O)CC(=O)c2ccc(O)c(OC)c2)ccc1O

InChI Key: InChIKey=WGRFGQJWSXSKER-ZZXKWVIFSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50020583   

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
Polyunsaturated fatty acid 5-lipoxygenase (Homo sapiens (Human))	BDBM50020583 (CHEMBL3290439) Show SMILES COc1cc(\C=C\C(=O)CC(=O)c2ccc(O)c(OC)c2)ccc1O Show InChI InChI=1S/C19H18O6/c1-24-18-9-12(4-7-15(18)21)3-6-14(20)11-17(23)13-5-8-16(22)19(10-13)25-2/h3-10,21-22H,11H2,1-2H3/b6-3+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.30E+3	n/a	n/a	n/a	n/a	n/a	n/a
University Jena Curated by ChEMBL					Assay Description Inhibition of human recombinant 5-LO expressed in Escherichia coli Bl21 (DE3) using arachidonic acid as substrate preincubated for 10 mins measured a...				J Med Chem 57: 5638-48 (2014) Article DOI: 10.1021/jm500308c BindingDB Entry DOI: 10.7270/Q2HT2QWN
					More data for this Ligand-Target Pair
Signal transducer and activator of transcription 3 (Homo sapiens (Human))	BDBM50020583 (CHEMBL3290439) Show SMILES COc1cc(\C=C\C(=O)CC(=O)c2ccc(O)c(OC)c2)ccc1O Show InChI InChI=1S/C19H18O6/c1-24-18-9-12(4-7-15(18)21)3-6-14(20)11-17(23)13-5-8-16(22)19(10-13)25-2/h3-10,21-22H,11H2,1-2H3/b6-3+	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.57E+4	n/a	n/a	n/a	n/a	n/a	n/a
University Jena Curated by ChEMBL					Assay Description Inhibition of STAT3 transcriptional activity in human HaCaT cells after 6 hrs by luciferase reporter gene assay				J Med Chem 57: 5638-48 (2014) Article DOI: 10.1021/jm500308c BindingDB Entry DOI: 10.7270/Q2HT2QWN
					More data for this Ligand-Target Pair
Polyunsaturated fatty acid 5-lipoxygenase (Homo sapiens (Human))	BDBM50020583 (CHEMBL3290439) Show SMILES COc1cc(\C=C\C(=O)CC(=O)c2ccc(O)c(OC)c2)ccc1O Show InChI InChI=1S/C19H18O6/c1-24-18-9-12(4-7-15(18)21)3-6-14(20)11-17(23)13-5-8-16(22)19(10-13)25-2/h3-10,21-22H,11H2,1-2H3/b6-3+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	9.90E+3	n/a	n/a	n/a	n/a	n/a	n/a
University Jena Curated by ChEMBL					Assay Description Inhibition of 5-LO in human neutrophils using arachidonic acid as substrate preincubated for 15 mins measured after 10 mins by HPLC analysis				J Med Chem 57: 5638-48 (2014) Article DOI: 10.1021/jm500308c BindingDB Entry DOI: 10.7270/Q2HT2QWN
					More data for this Ligand-Target Pair