Compile Data Set for Download or QSAR

Found 22 hits of ic50 for UniProtKB: P09811   

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 (Rattus norvegicus)	BDBM50135550 (4-{2-[(4-Chloro-pyridine-2-carbonyl)-amino]-3-fluo...) Show SMILES OC(=O)c1ccc(Oc2cccc(F)c2NC(=O)c2cc(Cl)ccn2)cc1C(O)=O Show InChI InChI=1S/C20H12ClFN2O6/c21-10-6-7-23-15(8-10)18(25)24-17-14(22)2-1-3-16(17)30-11-4-5-12(19(26)27)13(9-11)20(28)29/h1-9H,(H,24,25)(H,26,27)(H,28,29)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	<9	n/a	n/a	n/a	n/a	n/a	n/a
Merck Research Laboratories Curated by ChEMBL					Assay Description Inhibitory activity against rat 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, liver form (Rattus norvegicus)	BDBM50135552 (4-{2-[(4-Chloro-pyridine-2-carbonyl)-amino]-phenox...) Show SMILES OC(=O)c1ccc(Oc2ccccc2NC(=O)c2cc(Cl)ccn2)cc1C(O)=O Show InChI InChI=1S/C20H13ClN2O6/c21-11-7-8-22-16(9-11)18(24)23-15-3-1-2-4-17(15)29-12-5-6-13(19(25)26)14(10-12)20(27)28/h1-10H,(H,23,24)(H,25,26)(H,27,28)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	16	n/a	n/a	n/a	n/a	n/a	n/a
Merck Research Laboratories Curated by ChEMBL					Assay Description Inhibitory activity against rat 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, liver form (Rattus norvegicus)	BDBM50135563 (4-{2-[(4-Cyano-pyridine-2-carbonyl)-amino]-phenoxy...) Show SMILES OC(=O)c1ccc(Oc2ccccc2NC(=O)c2cc(ccn2)C#N)cc1C(O)=O Show InChI InChI=1S/C21H13N3O6/c22-11-12-7-8-23-17(9-12)19(25)24-16-3-1-2-4-18(16)30-13-5-6-14(20(26)27)15(10-13)21(28)29/h1-10H,(H,24,25)(H,26,27)(H,28,29)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	19	n/a	n/a	n/a	n/a	n/a	n/a
Merck Research Laboratories Curated by ChEMBL					Assay Description Inhibitory activity against rat 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, liver form (Rattus norvegicus)	BDBM50135556 (4-{2-[(4-Methoxy-pyridine-2-carbonyl)-amino]-pheno...) Show SMILES COc1ccnc(c1)C(=O)Nc1ccccc1Oc1ccc(C(O)=O)c(c1)C(O)=O Show InChI InChI=1S/C21H16N2O7/c1-29-12-8-9-22-17(11-12)19(24)23-16-4-2-3-5-18(16)30-13-6-7-14(20(25)26)15(10-13)21(27)28/h2-11H,1H3,(H,23,24)(H,25,26)(H,27,28)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	24	n/a	n/a	n/a	n/a	n/a	n/a
Merck Research Laboratories Curated by ChEMBL					Assay Description Inhibitory activity against rat 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, liver form (Rattus norvegicus)	BDBM50135549 (4-[3-Fluoro-2-(3-nitro-benzoylamino)-phenoxy]-phth...) Show SMILES OC(=O)c1ccc(Oc2cccc(F)c2NC(=O)c2cccc(c2)[N+]([O-])=O)cc1C(O)=O Show InChI InChI=1S/C21H13FN2O8/c22-16-5-2-6-17(32-13-7-8-14(20(26)27)15(10-13)21(28)29)18(16)23-19(25)11-3-1-4-12(9-11)24(30)31/h1-10H,(H,23,25)(H,26,27)(H,28,29)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	302	n/a	n/a	n/a	n/a	n/a	n/a
Merck Research Laboratories Curated by ChEMBL					Assay Description Inhibitory activity against rat 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, liver form (Rattus norvegicus)	BDBM50194701 ((2R,3R,4R)-2-Hydroxymethylpyrrolidin-3,4-diol hydr...) Show SMILES OC[C@H]1[NH2+]C[C@@H](O)[C@@H]1O Show InChI InChI=1S/C5H11NO3/c7-2-3-5(9)4(8)1-6-3/h3-9H,1-2H2/p+1/t3-,4-,5-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	370	n/a	n/a	n/a	n/a	n/a	n/a
The National Hellenic Research Foundation Curated by ChEMBL					Assay Description Inhibition of phosphorylated form of rat liver glycogen phosphorylase				J Med Chem 49: 5687-701 (2006) Article DOI: 10.1021/jm060496g BindingDB Entry DOI: 10.7270/Q25Q4VQP
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Rattus norvegicus)	BDBM50182801 ((3R,4R,5R)-5-(Hydroxymethyl)piperidine-3,4-diol, 8...) Show SMILES OC[C@H]1CNC[C@@H](O)[C@@H]1O |r| Show InChI InChI=1S/C6H13NO3/c8-3-4-1-7-2-5(9)6(4)10/h4-10H,1-3H2/t4-,5-,6-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE MMDB PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	680	n/a	n/a	n/a	n/a	n/a	n/a
The National Hellenic Research Foundation Curated by ChEMBL					Assay Description Inhibition of phosphorylated form of rat liver glycogen phosphorylase				J Med Chem 49: 5687-701 (2006) Article DOI: 10.1021/jm060496g BindingDB Entry DOI: 10.7270/Q25Q4VQP
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Rattus norvegicus)	BDBM50016703 (2-Hydroxymethyl-pyrrolidine-3,4-diol | BDBM5003148...) Show SMILES OC[C@H]1NC[C@@H](O)[C@@H]1O |r| Show InChI InChI=1S/C5H11NO3/c7-2-3-5(9)4(8)1-6-3/h3-9H,1-2H2/t3-,4-,5?/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid PDB UniChem Similars	Article PubMed	n/a	n/a	1.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
Daiichi Sankyo Co., Ltd. Curated by ChEMBL					Assay Description Inhibition of glycogen phosphorylase in rat hepatocytes assessed as reduction in basal glycogenolysis				Drug Metab Dispos 41: 878-87 (2013) Article DOI: 10.1124/dmd.112.050591 BindingDB Entry DOI: 10.7270/Q2TB18M8
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Rattus norvegicus)	BDBM50016703 (2-Hydroxymethyl-pyrrolidine-3,4-diol | BDBM5003148...) Show SMILES OC[C@H]1NC[C@@H](O)[C@@H]1O |r| Show InChI InChI=1S/C5H11NO3/c7-2-3-5(9)4(8)1-6-3/h3-9H,1-2H2/t3-,4-,5?/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid PDB UniChem Similars	Article PubMed	n/a	n/a	1.10E+3	n/a	n/a	n/a	n/a	n/a	n/a
Daiichi Sankyo Co., Ltd. Curated by ChEMBL					Assay Description Inhibition of glycogen phosphorylase in rat hepatocytes assessed as reduction in glucagom-induced glycogenolysis				Drug Metab Dispos 41: 878-87 (2013) Article DOI: 10.1124/dmd.112.050591 BindingDB Entry DOI: 10.7270/Q2TB18M8
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Rattus norvegicus)	BDBM50194702 ((3R,4R,5R)-5-(HYDROXYMETHYL)-1-(3-PHENYLPROPYL)PIP...) Show SMILES OC[C@H]1CN(CCCc2ccccc2)C[C@@H](O)[C@@H]1O Show InChI InChI=1S/C15H23NO3/c17-11-13-9-16(10-14(18)15(13)19)8-4-7-12-5-2-1-3-6-12/h1-3,5-6,13-15,17-19H,4,7-11H2/t13-,14-,15-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL DrugBank MMDB PC cid PC sid PDB UniChem Patents	Article PubMed	n/a	n/a	1.22E+3	n/a	n/a	n/a	n/a	n/a	n/a
The National Hellenic Research Foundation Curated by ChEMBL					Assay Description Inhibition of phosphorylated form of rat liver glycogen phosphorylase				J Med Chem 49: 5687-701 (2006) Article DOI: 10.1021/jm060496g BindingDB Entry DOI: 10.7270/Q25Q4VQP
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Rattus norvegicus)	BDBM50146091 (CHEMBL3765349) Show SMILES CC(=O)OC[C@H]1O[C@@]2(CC(=NO2)c2ccc3ccccc3c2)[C@H](OC(C)=O)[C@@H](OC(C)=O)[C@@H]1OC(C)=O |r,c:9| Show InChI InChI=1S/C26H27NO10/c1-14(28)32-13-22-23(33-15(2)29)24(34-16(3)30)25(35-17(4)31)26(36-22)12-21(27-37-26)20-10-9-18-7-5-6-8-19(18)11-20/h5-11,22-25H,12-13H2,1-4H3/t22-,23-,24+,25-,26-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.36E+4	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ Claude Bernard Lyon 1 Curated by ChEMBL					Assay Description Inhibition of glycogen phosphorylase in Wistar rat hepatocytes assessed as decrease in glucagon stimulated glucose release after 3 hrs by glucose oxi...				Eur J Med Chem 108: 444-54 (2016) Article DOI: 10.1016/j.ejmech.2015.12.004 BindingDB Entry DOI: 10.7270/Q2QR500M
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Rattus norvegicus)	BDBM50146082 (CHEMBL3763876) Show SMILES OC[C@H]1O[C@@]2(CC(=NO2)c2ccc3cc(O)ccc3c2)[C@H](O)[C@@H](O)[C@@H]1O |r,c:6| Show InChI InChI=1S/C18H19NO7/c20-8-14-15(22)16(23)17(24)18(25-14)7-13(19-26-18)11-2-1-10-6-12(21)4-3-9(10)5-11/h1-6,14-17,20-24H,7-8H2/t14-,15-,16+,17-,18-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.01E+4	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ Claude Bernard Lyon 1 Curated by ChEMBL					Assay Description Inhibition of glycogen phosphorylase in Wistar rat hepatocytes assessed as decrease in glucagon stimulated glucose release after 3 hrs by glucose oxi...				Eur J Med Chem 108: 444-54 (2016) Article DOI: 10.1016/j.ejmech.2015.12.004 BindingDB Entry DOI: 10.7270/Q2QR500M
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Rattus norvegicus)	BDBM34110 (glucopyranosylidene-spiro-isoxazoline, 4e) Show SMILES OC[C@H]1O[C@@]2(CC(=NO2)c2ccc3ccccc3c2)[C@H](O)[C@@H](O)[C@@H]1O |c:6| Show InChI InChI=1S/C18H19NO6/c20-9-14-15(21)16(22)17(23)18(24-14)8-13(19-25-18)12-6-5-10-3-1-2-4-11(10)7-12/h1-7,14-17,20-23H,8-9H2/t14-,15-,16+,17-,18-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.60E+4	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ Claude Bernard Lyon 1 Curated by ChEMBL					Assay Description Inhibition of glycogen phosphorylase in Wistar rat hepatocytes assessed as decrease in glucagon stimulated glucose release after 3 hrs by glucose oxi...				Eur J Med Chem 108: 444-54 (2016) Article DOI: 10.1016/j.ejmech.2015.12.004 BindingDB Entry DOI: 10.7270/Q2QR500M
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Rattus norvegicus)	BDBM50294476 ((E)-4-(naphthalen-2-yl)-1-((2S,3R,4R,5S,6R)-3,4,5-...) Show SMILES OC[C@H]1O[C@@H](CC(=O)C=Cc2ccc3ccccc3c2)[C@H](O)[C@@H](O)[C@@H]1O |r,w:8.7| Show InChI InChI=1S/C20H22O6/c21-11-17-19(24)20(25)18(23)16(26-17)10-15(22)8-6-12-5-7-13-3-1-2-4-14(13)9-12/h1-9,16-21,23-25H,10-11H2/t16-,17+,18-,19+,20+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	9.80E+4	n/a	n/a	n/a	n/a	n/a	n/a
Central Drug Research Institute Curated by ChEMBL					Assay Description Inhibition of rat liver glycogen phosphatase				Bioorg Med Chem Lett 19: 2699-703 (2009) Article DOI: 10.1016/j.bmcl.2009.03.136 BindingDB Entry DOI: 10.7270/Q20V8CTK
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Rattus norvegicus)	BDBM50175892 (2alpha,3beta-dihydroxy-12-oleanen-28-oic acid | 2a...) Show SMILES CC1(C)CC[C@@]2(CC[C@]3(C)C(=CC[C@@H]4[C@@]5(C)C[C@@H](O)[C@H](O)C(C)(C)[C@@H]5CC[C@@]34C)[C@@H]2C1)C(O)=O |r,c:10| Show InChI InChI=1S/C30H48O4/c1-25(2)12-14-30(24(33)34)15-13-28(6)18(19(30)16-25)8-9-22-27(5)17-20(31)23(32)26(3,4)21(27)10-11-29(22,28)7/h8,19-23,31-32H,9-17H2,1-7H3,(H,33,34)/t19-,20+,21-,22+,23-,27-,28+,29+,30-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	9.90E+4	n/a	n/a	n/a	n/a	n/a	n/a
China Pharmaceutical University Curated by ChEMBL					Assay Description Inhibitory concentration against rat liver glycogen phosphorylase				Bioorg Med Chem Lett 15: 4944-8 (2005) Article DOI: 10.1016/j.bmcl.2005.08.026 BindingDB Entry DOI: 10.7270/Q27M08R5
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Rattus norvegicus)	BDBM50146088 (CHEMBL3763929) Show SMILES OC[C@H]1O[C@@]2(CC(=NO2)c2ccc3OCOc3c2)[C@H](O)[C@@H](O)[C@@H]1O |r,c:6| Show InChI InChI=1S/C15H17NO8/c17-5-11-12(18)13(19)14(20)15(23-11)4-8(16-24-15)7-1-2-9-10(3-7)22-6-21-9/h1-3,11-14,17-20H,4-6H2/t11-,12-,13+,14-,15-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ Claude Bernard Lyon 1 Curated by ChEMBL					Assay Description Inhibition of glycogen phosphorylase in Wistar rat hepatocytes assessed as decrease in glucagon stimulated glucose release after 3 hrs by glucose oxi...				Eur J Med Chem 108: 444-54 (2016) Article DOI: 10.1016/j.ejmech.2015.12.004 BindingDB Entry DOI: 10.7270/Q2QR500M
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Rattus norvegicus)	BDBM50146090 (CHEMBL3763976) Show SMILES OC[C@H]1O[C@@]2(CC(=NO2)c2ccc3OCCOc3c2)[C@H](O)[C@@H](O)[C@@H]1O |r,c:6| Show InChI InChI=1S/C16H19NO8/c18-7-12-13(19)14(20)15(21)16(24-12)6-9(17-25-16)8-1-2-10-11(5-8)23-4-3-22-10/h1-2,5,12-15,18-21H,3-4,6-7H2/t12-,13-,14+,15-,16-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ Claude Bernard Lyon 1 Curated by ChEMBL					Assay Description Inhibition of glycogen phosphorylase in Wistar rat hepatocytes assessed as decrease in glucagon stimulated glucose release after 3 hrs by glucose oxi...				Eur J Med Chem 108: 444-54 (2016) Article DOI: 10.1016/j.ejmech.2015.12.004 BindingDB Entry DOI: 10.7270/Q2QR500M
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Rattus norvegicus)	BDBM50146085 (CHEMBL3764911) Show SMILES COc1cc(OC)cc(c1)C1=NO[C@@]2(C1)O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O |r,t:11| Show InChI InChI=1S/C16H21NO8/c1-22-9-3-8(4-10(5-9)23-2)11-6-16(25-17-11)15(21)14(20)13(19)12(7-18)24-16/h3-5,12-15,18-21H,6-7H2,1-2H3/t12-,13-,14+,15-,16-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ Claude Bernard Lyon 1 Curated by ChEMBL					Assay Description Inhibition of glycogen phosphorylase in Wistar rat hepatocytes assessed as decrease in glucagon stimulated glucose release after 3 hrs by glucose oxi...				Eur J Med Chem 108: 444-54 (2016) Article DOI: 10.1016/j.ejmech.2015.12.004 BindingDB Entry DOI: 10.7270/Q2QR500M
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Rattus norvegicus)	BDBM50146081 (CHEMBL3764195) Show SMILES OC[C@H]1O[C@@]2(CC(=NO2)c2cc3ccccc3c3ccccc23)[C@H](O)[C@@H](O)[C@@H]1O |r,c:6| Show InChI InChI=1S/C22H21NO6/c24-11-18-19(25)20(26)21(27)22(28-18)10-17(23-29-22)16-9-12-5-1-2-6-13(12)14-7-3-4-8-15(14)16/h1-9,18-21,24-27H,10-11H2/t18-,19-,20+,21-,22-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ Claude Bernard Lyon 1 Curated by ChEMBL					Assay Description Inhibition of glycogen phosphorylase in Wistar rat hepatocytes assessed as decrease in glucagon stimulated glucose release after 3 hrs by glucose oxi...				Eur J Med Chem 108: 444-54 (2016) Article DOI: 10.1016/j.ejmech.2015.12.004 BindingDB Entry DOI: 10.7270/Q2QR500M
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Rattus norvegicus)	BDBM50146086 (CHEMBL3764775) Show SMILES CSc1ccc(cc1)C1=NO[C@@]2(C1)O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O |r,t:9| Show InChI InChI=1S/C15H19NO6S/c1-23-9-4-2-8(3-5-9)10-6-15(22-16-10)14(20)13(19)12(18)11(7-17)21-15/h2-5,11-14,17-20H,6-7H2,1H3/t11-,12-,13+,14-,15-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ Claude Bernard Lyon 1 Curated by ChEMBL					Assay Description Inhibition of glycogen phosphorylase in Wistar rat hepatocytes assessed as decrease in glucagon stimulated glucose release after 3 hrs by glucose oxi...				Eur J Med Chem 108: 444-54 (2016) Article DOI: 10.1016/j.ejmech.2015.12.004 BindingDB Entry DOI: 10.7270/Q2QR500M
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Rattus norvegicus)	BDBM50222205 ((1S,2R,4aS,6aS,6bR,8aR,10R,11R,12aR,12bR,14bS)-10,...) Show SMILES C[C@@H]1CC[C@@]2(CC[C@]3(C)C(=CC[C@@H]4[C@@]5(C)C[C@@H](O)[C@H](O)C(C)(C)[C@@H]5CC[C@@]34C)[C@@H]2[C@H]1C)C(O)=O |r,c:9| Show InChI InChI=1S/C30H48O4/c1-17-10-13-30(25(33)34)15-14-28(6)19(23(30)18(17)2)8-9-22-27(5)16-20(31)24(32)26(3,4)21(27)11-12-29(22,28)7/h8,17-18,20-24,31-32H,9-16H2,1-7H3,(H,33,34)/t17-,18+,20-,21+,22-,23+,24+,27+,28-,29-,30+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.01E+5	n/a	n/a	n/a	n/a	n/a	n/a
China Pharmaceutical University Curated by ChEMBL					Assay Description Inhibitory concentration against rat liver glycogen phosphorylase				Bioorg Med Chem Lett 15: 4944-8 (2005) Article DOI: 10.1016/j.bmcl.2005.08.026 BindingDB Entry DOI: 10.7270/Q27M08R5
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Rattus norvegicus)	BDBM10849 (1,3,7-trimethyl-2,3,6,7-tetrahydro-1H-purine-2,6-d...) Show SMILES Cn1cnc2n(C)c(=O)n(C)c(=O)c12 Show InChI InChI=1S/C8H10N4O2/c1-10-4-9-6-5(10)7(13)12(3)8(14)11(6)2/h4H,1-3H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL DrugBank KEGG MMDB PC cid PC sid PDB UniChem Patents Similars	PDB Article PubMed	n/a	n/a	6.48E+5	n/a	n/a	n/a	n/a	n/a	n/a
China Pharmaceutical University Curated by ChEMBL					Assay Description Inhibitory concentration against rat liver glycogen phosphorylase				Bioorg Med Chem Lett 15: 4944-8 (2005) Article DOI: 10.1016/j.bmcl.2005.08.026 BindingDB Entry DOI: 10.7270/Q27M08R5
					More data for this Ligand-Target Pair				3D Structure (crystal)