null

SMILES: OC(=O)c1ccc(Oc2ccccc2NC(=O)c2cc(ccn2)[N+]([O-])=O)cc1C(O)=O

InChI Key: InChIKey=LIOKFTMUGRDMBH-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50135562   

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
Glycogen phosphorylase, liver form (Homo sapiens (Human))	BDBM50135562 (4-{2-[(4-Nitro-pyridine-2-carbonyl)-amino]-phenoxy...) Show SMILES OC(=O)c1ccc(Oc2ccccc2NC(=O)c2cc(ccn2)[N+]([O-])=O)cc1C(O)=O Show InChI InChI=1S/C20H13N3O8/c24-18(16-9-11(23(29)30)7-8-21-16)22-15-3-1-2-4-17(15)31-12-5-6-13(19(25)26)14(10-12)20(27)28/h1-10H,(H,22,24)(H,25,26)(H,27,28)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	3	n/a	n/a	n/a	n/a	n/a	n/a
Merck Research Laboratories Curated by ChEMBL					Assay Description Inhibitory activity against HLGP(human liver glycogen phosphorylase)				Bioorg Med Chem Lett 13: 4125-8 (2003) BindingDB Entry DOI: 10.7270/Q26M367F
					More data for this Ligand-Target Pair
Glycogen phosphorylase, muscle form (Homo sapiens (Human))	BDBM50135562 (4-{2-[(4-Nitro-pyridine-2-carbonyl)-amino]-phenoxy...) Show SMILES OC(=O)c1ccc(Oc2ccccc2NC(=O)c2cc(ccn2)[N+]([O-])=O)cc1C(O)=O Show InChI InChI=1S/C20H13N3O8/c24-18(16-9-11(23(29)30)7-8-21-16)22-15-3-1-2-4-17(15)31-12-5-6-13(19(25)26)14(10-12)20(27)28/h1-10H,(H,22,24)(H,25,26)(H,27,28)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	25	n/a	n/a	n/a	n/a	n/a	n/a
Merck Research Laboratories Curated by ChEMBL					Assay Description Inhibitory activity against HMGP(human muscle glycogen phosphorylase)				Bioorg Med Chem Lett 13: 4125-8 (2003) BindingDB Entry DOI: 10.7270/Q26M367F
					More data for this Ligand-Target Pair