null

SMILES: Cc1ccnc(c1)C(=O)Nc1cc2ccccc2cc1Oc1ccc(C(O)=O)c(c1)C(O)=O

InChI Key: InChIKey=WZJSYMIZGCAZDT-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50135560   

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, muscle form (Homo sapiens (Human))	BDBM50135560 (4-{3-[(4-Methyl-pyridine-2-carbonyl)-amino]-naphth...) Show SMILES Cc1ccnc(c1)C(=O)Nc1cc2ccccc2cc1Oc1ccc(C(O)=O)c(c1)C(O)=O Show InChI InChI=1S/C25H18N2O6/c1-14-8-9-26-21(10-14)23(28)27-20-11-15-4-2-3-5-16(15)12-22(20)33-17-6-7-18(24(29)30)19(13-17)25(31)32/h2-13H,1H3,(H,27,28)(H,29,30)(H,31,32)	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	57	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
Glycogen phosphorylase, liver form (Homo sapiens (Human))	BDBM50135560 (4-{3-[(4-Methyl-pyridine-2-carbonyl)-amino]-naphth...) Show SMILES Cc1ccnc(c1)C(=O)Nc1cc2ccccc2cc1Oc1ccc(C(O)=O)c(c1)C(O)=O Show InChI InChI=1S/C25H18N2O6/c1-14-8-9-26-21(10-14)23(28)27-20-11-15-4-2-3-5-16(15)12-22(20)33-17-6-7-18(24(29)30)19(13-17)25(31)32/h2-13H,1H3,(H,27,28)(H,29,30)(H,31,32)	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	10	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