Compile Data Set for Download or QSAR

Found 2 hits Enz. Inhib. hit(s) with Target = 'Glycogen phosphorylase, liver form' and Ligand = 'BDBM50136439'   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kJ/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))	BDBM50136439 (4-Chloro-1H-indole-2-carboxylic acid (1-methyl-2-o...) Show SMILES CN1C(=O)C(Cc2ccccc12)NC(=O)c1cc2c(Cl)cccc2[nH]1 Show InChI InChI=1S/C19H16ClN3O2/c1-23-17-8-3-2-5-11(17)9-16(19(23)25)22-18(24)15-10-12-13(20)6-4-7-14(12)21-15/h2-8,10,16,21H,9H2,1H3,(H,22,24)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.60E+3	n/a	n/a	n/a	n/a	n/a	n/a
Applied Science University Curated by ChEMBL					Assay Description Inhibition of human liver glycogen phosphorylase 1a assessed as release of phosphate from glucose-1- phosphate after 20 mins				Bioorg Med Chem 19: 4746-71 (2011) Article DOI: 10.1016/j.bmc.2011.06.086 BindingDB Entry DOI: 10.7270/Q2028RXJ
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Homo sapiens (Human))	BDBM50136439 (4-Chloro-1H-indole-2-carboxylic acid (1-methyl-2-o...) Show SMILES CN1C(=O)C(Cc2ccccc12)NC(=O)c1cc2c(Cl)cccc2[nH]1 Show InChI InChI=1S/C19H16ClN3O2/c1-23-17-8-3-2-5-11(17)9-16(19(23)25)22-18(24)15-10-12-13(20)6-4-7-14(12)21-15/h2-8,10,16,21H,9H2,1H3,(H,22,24)	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	1.60E+3	n/a	n/a	n/a	n/a	n/a	n/a
Merck Research Laboratories Curated by ChEMBL					Assay Description Inhibitory concentration against recombinant human liver glycogen phosphorylase a (HLGPa)				Bioorg Med Chem Lett 13: 4385-8 (2003) BindingDB Entry DOI: 10.7270/Q2S75FQV
					More data for this Ligand-Target Pair