null

SMILES: OC(=O)c1ccc(cc1)N=Nc1ccc(O)c2ncccc12

InChI Key: InChIKey=WHYSDEAUKYVHBQ-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50343659   

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
Lactoylglutathione lyase (Homo sapiens (Human))	BDBM50343659 ((E)-4-((8-hydroxyquinolin-5-yl)diazenyl)benzoic ac...) Show SMILES OC(=O)c1ccc(cc1)N=Nc1ccc(O)c2ncccc12 |w:9.9| Show InChI InChI=1S/C16H11N3O3/c20-14-8-7-13(12-2-1-9-17-15(12)14)19-18-11-5-3-10(4-6-11)16(21)22/h1-9,20H,(H,21,22)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem		n/a	n/a	4.45E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details
					More data for this Ligand-Target Pair
Ribosomal protein S6 kinase alpha-3 (Homo sapiens (Human))	BDBM50343659 ((E)-4-((8-hydroxyquinolin-5-yl)diazenyl)benzoic ac...) Show SMILES OC(=O)c1ccc(cc1)N=Nc1ccc(O)c2ncccc12 |w:9.9| Show InChI InChI=1S/C16H11N3O3/c20-14-8-7-13(12-2-1-9-17-15(12)14)19-18-11-5-3-10(4-6-11)16(21)22/h1-9,20H,(H,21,22)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.47E+3	n/a	n/a	n/a	n/a	n/a	n/a
East China University of Science and Technology Curated by ChEMBL					Assay Description Inhibition of RSK2 after 60 mins				J Med Chem 54: 3564-74 (2011) Article DOI: 10.1021/jm200139j BindingDB Entry DOI: 10.7270/Q26M374H
					More data for this Ligand-Target Pair