Compile Data Set for Download or QSAR

Found 2 hits Enz. Inhib. hit(s) with Target = 'Glycogen phosphorylase, liver form' and Ligand = 'BDBM50136420'   

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))	BDBM50136420 (5-Chloro-1H-indole-2-carboxylic acid (2-oxo-1-pyri...) Show SMILES Clc1ccc2[nH]c(cc2c1)C(=O)NC1Cc2ccccc2N(Cc2cccnc2)C1=O Show InChI InChI=1S/C24H19ClN4O2/c25-18-7-8-19-17(10-18)12-20(27-19)23(30)28-21-11-16-5-1-2-6-22(16)29(24(21)31)14-15-4-3-9-26-13-15/h1-10,12-13,21,27H,11,14H2,(H,28,30)	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	130	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))	BDBM50136420 (5-Chloro-1H-indole-2-carboxylic acid (2-oxo-1-pyri...) Show SMILES Clc1ccc2[nH]c(cc2c1)C(=O)NC1Cc2ccccc2N(Cc2cccnc2)C1=O Show InChI InChI=1S/C24H19ClN4O2/c25-18-7-8-19-17(10-18)12-20(27-19)23(30)28-21-11-16-5-1-2-6-22(16)29(24(21)31)14-15-4-3-9-26-13-15/h1-10,12-13,21,27H,11,14H2,(H,28,30)	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	130	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