Compile Data Set for Download or QSAR

Found 65 hits of ki for UniProtKB: P11217   

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))	BDBM50056221 (CHEMBL3322297) Show SMILES OC(=O)C1=C(NC=CC1)C(O)=O |c:6,t:3| Show InChI InChI=1S/C7H7NO4/c9-6(10)4-2-1-3-8-5(4)7(11)12/h1,3,8H,2H2,(H,9,10)(H,11,12)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	1.60	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Thessaly Curated by ChEMBL					Assay Description Inhibition of glycogen phosphorylase b (unknown origin)				Bioorg Med Chem 22: 4810-25 (2014) Article DOI: 10.1016/j.bmc.2014.06.058 BindingDB Entry DOI: 10.7270/Q2KS6T58
					More data for this Ligand-Target Pair
Glycogen phosphorylase, muscle form (Homo sapiens (Human))	BDBM50149297 ((S)-1-Ethyl-6-methyl-4-phenyl-1,4-dihydro-pyridine...) Show SMILES CCN1C(C)=C([C@H](C(C(O)=O)=C1C(O)=O)c1ccccc1)C(=O)OC(C)C |c:4,10| Show InChI InChI=1S/C20H23NO6/c1-5-21-12(4)14(20(26)27-11(2)3)15(13-9-7-6-8-10-13)16(18(22)23)17(21)19(24)25/h6-11,15H,5H2,1-4H3,(H,22,23)(H,24,25)/t15-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	11	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Novo Nordisk A/S Curated by ChEMBL					Assay Description Inhibitory activity against rabbit muscle glycogen phosphorylase a in the absence of AMP				J Med Chem 47: 3537-45 (2004) Article DOI: 10.1021/jm031121n BindingDB Entry DOI: 10.7270/Q2HM5977
					More data for this Ligand-Target Pair
Glycogen phosphorylase, muscle form (Homo sapiens (Human))	BDBM50386288 (CHEMBL2041081) Show SMILES OC[C@H]1O[C@H]([C@H](O)[C@@H](O)[C@@H]1O)n1cc(Cl)c(=O)[nH]c1=O |r| Show InChI InChI=1S/C10H13ClN2O7/c11-3-1-13(10(19)12-8(3)18)9-7(17)6(16)5(15)4(2-14)20-9/h1,4-7,9,14-17H,2H2,(H,12,18,19)/t4-,5-,6+,7-,9-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL MMDB PC cid PC sid PDB UniChem Similars	PDB Article PubMed	1.02E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Thessaly Curated by ChEMBL					Assay Description Inhibition of glycogen phosphorylase b				Eur J Med Chem 54: 740-9 (2012) Article DOI: 10.1016/j.ejmech.2012.06.029 BindingDB Entry DOI: 10.7270/Q2VX0HKH
					More data for this Ligand-Target Pair				3D Structure (crystal)
Glycogen phosphorylase, muscle form (Homo sapiens (Human))	BDBM50386290 (CHEMBL2040853) Show SMILES OC[C@H]1O[C@H]([C@H](O)[C@@H](O)[C@@H]1O)n1cc(I)c(=O)[nH]c1=O |r| Show InChI InChI=1S/C10H13IN2O7/c11-3-1-13(10(19)12-8(3)18)9-7(17)6(16)5(15)4(2-14)20-9/h1,4-7,9,14-17H,2H2,(H,12,18,19)/t4-,5-,6+,7-,9-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL MMDB PC cid PC sid PDB UniChem Similars	PDB Article PubMed	1.94E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Thessaly Curated by ChEMBL					Assay Description Inhibition of glycogen phosphorylase b				Eur J Med Chem 54: 740-9 (2012) Article DOI: 10.1016/j.ejmech.2012.06.029 BindingDB Entry DOI: 10.7270/Q2VX0HKH
					More data for this Ligand-Target Pair				3D Structure (crystal)
Glycogen phosphorylase, muscle form (Homo sapiens (Human))	BDBM50149315 ((6S,7S,8R,9R)-6,7,8-Trihydroxy-9-hydroxymethyl-1,3...) Show SMILES OC[C@H]1C[C@@]2(NC(=O)NC2=O)[C@H](O)[C@@H](O)[C@@H]1O Show InChI InChI=1S/C9H14N2O6/c12-2-3-1-9(6(15)5(14)4(3)13)7(16)10-8(17)11-9/h3-6,12-15H,1-2H2,(H2,10,11,16,17)/t3-,4-,5+,6-,9-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	3.00E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Novo Nordisk A/S Curated by ChEMBL					Assay Description Inhibitory activity against rabbit Muscle glycogen phosphorylase b				J Med Chem 47: 3537-45 (2004) Article DOI: 10.1021/jm031121n BindingDB Entry DOI: 10.7270/Q2HM5977
					More data for this Ligand-Target Pair
Glycogen phosphorylase, muscle form (Homo sapiens (Human))	BDBM50057754 (8,9,10-Trihydroxy-7-hydroxymethyl-6-oxa-1,3-diaza-...) Show SMILES OCC1OC2(NC(=O)NC2=O)C(O)C(O)C1O Show InChI InChI=1S/C8H12N2O7/c11-1-2-3(12)4(13)5(14)8(17-2)6(15)9-7(16)10-8/h2-5,11-14H,1H2,(H2,9,10,15,16)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid PDB UniChem Similars	PDB Article PubMed	3.02E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Alcala Curated by ChEMBL					Assay Description Inhibitory activity against rabbit muscle glycogen phosphorylase				J Med Chem 40: 4089-102 (1998) Checked by Author Article DOI: 10.1021/jm970273d BindingDB Entry DOI: 10.7270/Q2S46TGM
					More data for this Ligand-Target Pair				3D Structure (crystal)
Glycogen phosphorylase, muscle form (Homo sapiens (Human))	BDBM50386289 (CHEMBL2041082) Show SMILES OC[C@H]1O[C@H]([C@H](O)[C@@H](O)[C@@H]1O)n1cc(Br)c(=O)[nH]c1=O |r| Show InChI InChI=1S/C10H13BrN2O7/c11-3-1-13(10(19)12-8(3)18)9-7(17)6(16)5(15)4(2-14)20-9/h1,4-7,9,14-17H,2H2,(H,12,18,19)/t4-,5-,6+,7-,9-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL MMDB PC cid PC sid PDB UniChem Similars	PDB Article PubMed	3.27E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Thessaly Curated by ChEMBL					Assay Description Inhibition of glycogen phosphorylase b				Eur J Med Chem 54: 740-9 (2012) Article DOI: 10.1016/j.ejmech.2012.06.029 BindingDB Entry DOI: 10.7270/Q2VX0HKH
					More data for this Ligand-Target Pair				3D Structure (crystal)
Glycogen phosphorylase, muscle form (Homo sapiens (Human))	BDBM50215446 (CHEMBL3351144) Show SMILES OC[C@@H]1O[C@@]2(NC(=O)NC2=O)[C@@H](O)[C@@H](O)[C@@H]1O |r| Show InChI InChI=1S/C8H12N2O7/c11-1-2-3(12)4(13)5(14)8(17-2)6(15)9-7(16)10-8/h2-5,11-14H,1H2,(H2,9,10,15,16)/t2-,3+,4-,5-,8-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	PubMed	4.20E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Lajos Kossuth University Curated by ChEMBL					Assay Description Inhibitor constant was measured against Muscle phosphorylase b in rabbit				Bioorg Med Chem Lett 9: 1385-90 (1999) BindingDB Entry DOI: 10.7270/Q2W66M82
					More data for this Ligand-Target Pair
Glycogen phosphorylase, muscle form (Homo sapiens (Human))	BDBM50215446 (CHEMBL3351144) Show SMILES OC[C@@H]1O[C@@]2(NC(=O)NC2=O)[C@@H](O)[C@@H](O)[C@@H]1O |r| Show InChI InChI=1S/C8H12N2O7/c11-1-2-3(12)4(13)5(14)8(17-2)6(15)9-7(16)10-8/h2-5,11-14H,1H2,(H2,9,10,15,16)/t2-,3+,4-,5-,8-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	PubMed	4.20E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Lajos Kossuth University Curated by ChEMBL					Assay Description Inhibitor constant was measured against Liver phosphorylase b in rat				Bioorg Med Chem Lett 9: 1385-90 (1999) BindingDB Entry DOI: 10.7270/Q2W66M82
					More data for this Ligand-Target Pair
Glycogen phosphorylase, muscle form (Homo sapiens (Human))	BDBM50330796 (4-Fluoro-benzaldehyde4-(beta-D-glucopyranosyl)thio...) Show SMILES CC[C@H]1O[C@@H](NC(=S)NN=Cc2ccc(F)cc2)[C@H](O)[C@@H](O)[C@@H]1O |r,w:9.8| Show InChI InChI=1S/C15H20FN3O4S/c1-2-10-11(20)12(21)13(22)14(23-10)18-15(24)19-17-7-8-3-5-9(16)6-4-8/h3-7,10-14,20-22H,2H2,1H3,(H2,18,19,24)/t10-,11-,12+,13-,14-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	4.60E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Hellenic Research Foundation Curated by ChEMBL					Assay Description Inhibition of glycogen phosphorylase b				Bioorg Med Chem 18: 7911-22 (2010) Article DOI: 10.1016/j.bmc.2010.09.039 BindingDB Entry DOI: 10.7270/Q2DV1K3Q
					More data for this Ligand-Target Pair
Glycogen phosphorylase, muscle form (Homo sapiens (Human))	BDBM50263769 ((5S,7R,8S,9S,10R)-8,9,10-Trihydroxy-7-hydroxymethy...) Show SMILES OC[C@H]1O[C@@]2(NC(=S)NC2=O)[C@H](O)[C@@H](O)[C@@H]1O |r| Show InChI InChI=1S/C8H12N2O6S/c11-1-2-3(12)4(13)5(14)8(16-2)6(15)9-7(17)10-8/h2-5,11-14H,1H2,(H2,9,10,15,17)/t2-,3-,4+,5-,8+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL MMDB PC cid PC sid PDB UniChem Similars	MMDB PDB PubMed	5.10E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Lajos Kossuth University Curated by ChEMBL					Assay Description Inhibitor constant was measured against Muscle phosphorylase b in rabbit				Bioorg Med Chem Lett 9: 1385-90 (1999) BindingDB Entry DOI: 10.7270/Q2W66M82
					More data for this Ligand-Target Pair				3D Structure (crystal)
Glycogen phosphorylase, muscle form (Homo sapiens (Human))	BDBM50263769 ((5S,7R,8S,9S,10R)-8,9,10-Trihydroxy-7-hydroxymethy...) Show SMILES OC[C@H]1O[C@@]2(NC(=S)NC2=O)[C@H](O)[C@@H](O)[C@@H]1O |r| Show InChI InChI=1S/C8H12N2O6S/c11-1-2-3(12)4(13)5(14)8(16-2)6(15)9-7(17)10-8/h2-5,11-14H,1H2,(H2,9,10,15,17)/t2-,3-,4+,5-,8+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL MMDB PC cid PC sid PDB UniChem Similars	MMDB PDB PubMed	1.09E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Lajos Kossuth University Curated by ChEMBL					Assay Description Inhibitor constant was measured against Muscle phosphorylase a in rabbit				Bioorg Med Chem Lett 9: 1385-90 (1999) BindingDB Entry DOI: 10.7270/Q2W66M82
					More data for this Ligand-Target Pair				3D Structure (crystal)
Glycogen phosphorylase, muscle form (Homo sapiens (Human))	BDBM50215446 (CHEMBL3351144) Show SMILES OC[C@@H]1O[C@@]2(NC(=O)NC2=O)[C@@H](O)[C@@H](O)[C@@H]1O |r| Show InChI InChI=1S/C8H12N2O7/c11-1-2-3(12)4(13)5(14)8(17-2)6(15)9-7(16)10-8/h2-5,11-14H,1H2,(H2,9,10,15,16)/t2-,3+,4-,5-,8-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	PubMed	2.60E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Lajos Kossuth University Curated by ChEMBL					Assay Description Inhibitor constant was measured against Muscle phosphorylase a in rabbit				Bioorg Med Chem Lett 9: 1385-90 (1999) BindingDB Entry DOI: 10.7270/Q2W66M82
					More data for this Ligand-Target Pair
Glycogen phosphorylase, muscle form (Homo sapiens (Human))	BDBM50240802 (1-N-ACETYL-BETA-D-GLUCOSAMINE | CHEMBL335315 | N-(...) Show SMILES CC(=O)N[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O |r| Show InChI InChI=1S/C8H15NO6/c1-3(11)9-8-7(14)6(13)5(12)4(2-10)15-8/h4-8,10,12-14H,2H2,1H3,(H,9,11)/t4-,5-,6+,7-,8-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MMDB PC cid PC sid PDB UniChem Patents Similars	PDB Article PubMed	3.16E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Alcala Curated by ChEMBL					Assay Description Inhibitory activity against rabbit muscle glycogen phosphorylase				J Med Chem 40: 4089-102 (1998) Checked by Author Article DOI: 10.1021/jm970273d BindingDB Entry DOI: 10.7270/Q2S46TGM
					More data for this Ligand-Target Pair				3D Structure (crystal)
Glycogen phosphorylase, muscle form (Homo sapiens (Human))	BDBM50422220 (CHEMBL334587) Show SMILES CCC(=O)N[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O Show InChI InChI=1S/C9H17NO6/c1-2-5(12)10-9-8(15)7(14)6(13)4(3-11)16-9/h4,6-9,11,13-15H,2-3H2,1H3,(H,10,12)/t4-,6-,7+,8-,9-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	3.89E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Alcala Curated by ChEMBL					Assay Description Inhibitory activity against rabbit muscle glycogen phosphorylase				J Med Chem 40: 4089-102 (1998) Checked by Author Article DOI: 10.1021/jm970273d BindingDB Entry DOI: 10.7270/Q2S46TGM
					More data for this Ligand-Target Pair
Glycogen phosphorylase, muscle form (Homo sapiens (Human))	BDBM50454688 (CHEMBL32811) Show SMILES OCC1OC2(NC(=O)N(O)C2=O)C(O)C(O)C1O Show InChI InChI=1S/C8H12N2O8/c11-1-2-3(12)4(13)5(14)8(18-2)6(15)10(17)7(16)9-8/h2-5,11-14,17H,1H2,(H,9,16)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid PDB UniChem Similars	PDB Article PubMed	3.89E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Alcala Curated by ChEMBL					Assay Description Inhibitory activity against rabbit muscle glycogen phosphorylase				J Med Chem 40: 4089-102 (1998) Checked by Author Article DOI: 10.1021/jm970273d BindingDB Entry DOI: 10.7270/Q2S46TGM
					More data for this Ligand-Target Pair				3D Structure (crystal)
Glycogen phosphorylase, muscle form (Homo sapiens (Human))	BDBM50057746 (2-Bromo-N-(3,4,5-trihydroxy-6-hydroxymethyl-tetrah...) Show SMILES OCC1OC(NC(=O)CBr)C(O)C(O)C1O Show InChI InChI=1S/C8H14BrNO6/c9-1-4(12)10-8-7(15)6(14)5(13)3(2-11)16-8/h3,5-8,11,13-15H,1-2H2,(H,10,12)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	4.37E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Alcala Curated by ChEMBL					Assay Description Inhibitory activity against rabbit muscle glycogen phosphorylase				J Med Chem 40: 4089-102 (1998) Checked by Author Article DOI: 10.1021/jm970273d BindingDB Entry DOI: 10.7270/Q2S46TGM
					More data for this Ligand-Target Pair
Glycogen phosphorylase, muscle form (Homo sapiens (Human))	BDBM50422216 (CHEMBL336310) Show SMILES OC[C@H]1O[C@@H](NC(=O)CCl)[C@H](O)[C@@H](O)[C@@H]1O Show InChI InChI=1S/C8H14ClNO6/c9-1-4(12)10-8-7(15)6(14)5(13)3(2-11)16-8/h3,5-8,11,13-15H,1-2H2,(H,10,12)/t3-,5-,6+,7-,8-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	4.47E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Alcala Curated by ChEMBL					Assay Description Inhibitory activity against rabbit muscle glycogen phosphorylase				J Med Chem 40: 4089-102 (1998) Checked by Author Article DOI: 10.1021/jm970273d BindingDB Entry DOI: 10.7270/Q2S46TGM
					More data for this Ligand-Target Pair
Glycogen phosphorylase, muscle form (Homo sapiens (Human))	BDBM50057742 (9,10,11-Trihydroxy-8-hydroxymethyl-7-oxa-1,4-diaza...) Show SMILES OCC1OC2(NC(=O)CNC2=O)C(O)C(O)C1O Show InChI InChI=1S/C9H14N2O7/c12-2-3-5(14)6(15)7(16)9(18-3)8(17)10-1-4(13)11-9/h3,5-7,12,14-16H,1-2H2,(H,10,17)(H,11,13)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	6.03E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Alcala Curated by ChEMBL					Assay Description Inhibitory activity against rabbit muscle glycogen phosphorylase				J Med Chem 40: 4089-102 (1998) Checked by Author Article DOI: 10.1021/jm970273d BindingDB Entry DOI: 10.7270/Q2S46TGM
					More data for this Ligand-Target Pair
Glycogen phosphorylase, muscle form (Homo sapiens (Human))	BDBM50240801 (CHEMBL131967 | N-((2R,3R,4S,5S,6R)-3,4,5-trihydrox...) Show SMILES OC[C@H]1O[C@@H](NC(=O)c2ccccc2)[C@H](O)[C@@H](O)[C@@H]1O |r| Show InChI InChI=1S/C13H17NO6/c15-6-8-9(16)10(17)11(18)13(20-8)14-12(19)7-4-2-1-3-5-7/h1-5,8-11,13,15-18H,6H2,(H,14,19)/t8-,9-,10+,11-,13-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL MMDB PC cid PC sid PDB UniChem Similars	MMDB PDB Article PubMed	8.13E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Alcala Curated by ChEMBL					Assay Description Inhibitory activity against rabbit muscle glycogen phosphorylase				J Med Chem 40: 4089-102 (1998) Checked by Author Article DOI: 10.1021/jm970273d BindingDB Entry DOI: 10.7270/Q2S46TGM
					More data for this Ligand-Target Pair				3D Structure (crystal)
Glycogen phosphorylase, muscle form (Homo sapiens (Human))	BDBM50422223 (CHEMBL423714) Show SMILES CCCC(=O)N[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O Show InChI InChI=1S/C10H19NO6/c1-2-3-6(13)11-10-9(16)8(15)7(14)5(4-12)17-10/h5,7-10,12,14-16H,2-4H2,1H3,(H,11,13)/t5-,7-,8+,9-,10-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	9.33E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Alcala Curated by ChEMBL					Assay Description Inhibitory activity against rabbit muscle glycogen phosphorylase				J Med Chem 40: 4089-102 (1998) Checked by Author Article DOI: 10.1021/jm970273d BindingDB Entry DOI: 10.7270/Q2S46TGM
					More data for this Ligand-Target Pair
Glycogen phosphorylase, muscle form (Homo sapiens (Human))	BDBM50363870 (CHEMBL132020) Show SMILES NC(=O)N[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O Show InChI InChI=1S/C7H14N2O6/c8-7(14)9-6-5(13)4(12)3(11)2(1-10)15-6/h2-6,10-13H,1H2,(H3,8,9,14)/t2-,3-,4+,5-,6-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.41E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Alcala Curated by ChEMBL					Assay Description Inhibitory activity against rabbit muscle glycogen phosphorylase				J Med Chem 40: 4089-102 (1998) Checked by Author Article DOI: 10.1021/jm970273d BindingDB Entry DOI: 10.7270/Q2S46TGM
					More data for this Ligand-Target Pair
Glycogen phosphorylase, muscle form (Homo sapiens (Human))	BDBM50057745 (3-Amino-8,9,10-trihydroxy-7-hydroxymethyl-6-oxa-1,...) Show SMILES NN1C(=O)NC2(OC(CO)C(O)C(O)C2O)C1=O Show InChI InChI=1S/C8H13N3O7/c9-11-6(16)8(10-7(11)17)5(15)4(14)3(13)2(1-12)18-8/h2-5,12-15H,1,9H2,(H,10,17)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid PDB UniChem Similars	PDB Article PubMed	1.45E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Alcala Curated by ChEMBL					Assay Description Inhibitory activity against rabbit muscle glycogen phosphorylase				J Med Chem 40: 4089-102 (1998) Checked by Author Article DOI: 10.1021/jm970273d BindingDB Entry DOI: 10.7270/Q2S46TGM
					More data for this Ligand-Target Pair				3D Structure (crystal)
Glycogen phosphorylase, muscle form (Homo sapiens (Human))	BDBM50057725 ((3,4,5-Trihydroxy-6-hydroxymethyl-tetrahydro-pyran...) Show SMILES [H][C@@]1(NC(=O)OCc2ccccc2)O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O Show InChI InChI=1S/C14H19NO7/c16-6-9-10(17)11(18)12(19)13(22-9)15-14(20)21-7-8-4-2-1-3-5-8/h1-5,9-13,16-19H,6-7H2,(H,15,20)/t9-,10-,11+,12-,13-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	3.47E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Alcala Curated by ChEMBL					Assay Description Inhibitory activity against rabbit muscle glycogen phosphorylase				J Med Chem 40: 4089-102 (1998) Checked by Author Article DOI: 10.1021/jm970273d BindingDB Entry DOI: 10.7270/Q2S46TGM
					More data for this Ligand-Target Pair
Glycogen phosphorylase, muscle form (Homo sapiens (Human))	BDBM50057755 (2-Amino-N-(3,4,5-trihydroxy-6-hydroxymethyl-tetrah...) Show SMILES NCC(=O)NC1OC(CO)C(O)C(O)C1O Show InChI InChI=1S/C8H16N2O6/c9-1-4(12)10-8-7(15)6(14)5(13)3(2-11)16-8/h3,5-8,11,13-15H,1-2,9H2,(H,10,12)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	3.72E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Alcala Curated by ChEMBL					Assay Description Inhibitory activity against rabbit muscle glycogen phosphorylase				J Med Chem 40: 4089-102 (1998) Checked by Author Article DOI: 10.1021/jm970273d BindingDB Entry DOI: 10.7270/Q2S46TGM
					More data for this Ligand-Target Pair
Glycogen phosphorylase, muscle form (Homo sapiens (Human))	BDBM50454694 (CHEMBL35457) Show SMILES CC(=O)NN1C(=O)NC2(OC(CO)C(O)C(O)C2O)C1=O Show InChI InChI=1S/C10H15N3O8/c1-3(15)12-13-8(19)10(11-9(13)20)7(18)6(17)5(16)4(2-14)21-10/h4-7,14,16-18H,2H2,1H3,(H,11,20)(H,12,15)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid PDB UniChem Similars	PDB Article PubMed	5.50E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Alcala Curated by ChEMBL					Assay Description Inhibitory activity against rabbit muscle glycogen phosphorylase				J Med Chem 40: 4089-102 (1998) Checked by Author Article DOI: 10.1021/jm970273d BindingDB Entry DOI: 10.7270/Q2S46TGM
					More data for this Ligand-Target Pair				3D Structure (crystal)
Glycogen phosphorylase, muscle form (Homo sapiens (Human))	BDBM50056222 (CHEMBL3322298) Show SMILES [H][C@]1(O[C@H]2[C@H](O)[C@@H](O)[C@@]([H])(O[C@H]3[C@H](O)[C@@H](O)[C@@]([H])(O[C@H]4[C@H](O)[C@@H](O)[C@@]([H])(O[C@H]5[C@H](O)[C@@H](O)[C@@]([H])(O[C@H]6[C@H](O)[C@@H](O)[C@@]([H])(O[C@H]7[C@H](O)[C@@H](O)C(O)O[C@@H]7CO)O[C@@H]6CO)O[C@@H]5CO)O[C@@H]4CO)O[C@@H]3CO)O[C@@H]2CO)O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O |r| Show InChI InChI=1S/C42H72O36/c43-1-8-15(50)16(51)24(59)37(67-8)74-31-10(3-45)69-39(26(61)18(31)53)76-33-12(5-47)71-41(28(63)20(33)55)78-35-14(7-49)72-42(29(64)22(35)57)77-34-13(6-48)70-40(27(62)21(34)56)75-32-11(4-46)68-38(25(60)19(32)54)73-30-9(2-44)66-36(65)23(58)17(30)52/h8-65H,1-7H2/t8-,9-,10-,11-,12-,13-,14-,15-,16+,17-,18-,19-,20-,21-,22-,23-,24-,25-,26-,27-,28-,29-,30-,31-,32-,33-,34-,35-,36?,37-,38-,39-,40-,41-,42-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL KEGG PC cid PC sid UniChem Similars	Article PubMed	1.00E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Thessaly Curated by ChEMBL					Assay Description Inhibition of glycogen phosphorylase b (unknown origin)				Bioorg Med Chem 22: 4810-25 (2014) Article DOI: 10.1016/j.bmc.2014.06.058 BindingDB Entry DOI: 10.7270/Q2KS6T58
					More data for this Ligand-Target Pair
Glycogen phosphorylase, muscle form (Homo sapiens (Human))	BDBM50422219 (CHEMBL133222) Show SMILES CC(=O)NCC(=O)N[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O Show InChI InChI=1S/C10H18N2O7/c1-4(14)11-2-6(15)12-10-9(18)8(17)7(16)5(3-13)19-10/h5,7-10,13,16-18H,2-3H2,1H3,(H,11,14)(H,12,15)/t5-,7-,8+,9-,10-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.00E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Alcala Curated by ChEMBL					Assay Description Inhibitory activity against rabbit muscle glycogen phosphorylase				J Med Chem 40: 4089-102 (1998) Checked by Author Article DOI: 10.1021/jm970273d BindingDB Entry DOI: 10.7270/Q2S46TGM
					More data for this Ligand-Target Pair
Glycogen phosphorylase, muscle form (Homo sapiens (Human))	BDBM50057758 (3,4,5-Trihydroxy-6-hydroxymethyl-tetrahydro-pyran-...) Show SMILES OCC1OC(C(O)C(O)C1O)C(=O)NC1CC1 Show InChI InChI=1S/C10H17NO6/c12-3-5-6(13)7(14)8(15)9(17-5)10(16)11-4-1-2-4/h4-9,12-15H,1-3H2,(H,11,16)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.29E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Alcala Curated by ChEMBL					Assay Description Inhibitory activity against rabbit muscle glycogen phosphorylase				J Med Chem 40: 4089-102 (1998) Checked by Author Article DOI: 10.1021/jm970273d BindingDB Entry DOI: 10.7270/Q2S46TGM
					More data for this Ligand-Target Pair
Glycogen phosphorylase, muscle form (Homo sapiens (Human))	BDBM50408121 (CHEMBL338719) Show SMILES OC[C@H]1O[C@H](CN=[N+]=[N-])[C@H](O)[C@@H](O)[C@@H]1O Show InChI InChI=1S/C7H13N3O5/c8-10-9-1-3-5(12)7(14)6(13)4(2-11)15-3/h3-7,11-14H,1-2H2/t3-,4-,5+,6-,7-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.65E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Alcala Curated by ChEMBL					Assay Description Inhibitory activity against rabbit muscle glycogen phosphorylase				J Med Chem 40: 4089-102 (1998) Checked by Author Article DOI: 10.1021/jm970273d BindingDB Entry DOI: 10.7270/Q2S46TGM
					More data for this Ligand-Target Pair
Glycogen phosphorylase, muscle form (Homo sapiens (Human))	BDBM50351158 (CHEMBL423707) Show SMILES OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@@H]1O |r| Show InChI InChI=1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3-,4+,5-,6+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG MMDB PC cid PC sid UniChem Patents Similars	Article PubMed	1.70E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Thessaly Curated by ChEMBL					Assay Description Inhibition of glycogen phosphorylase b (unknown origin)				Bioorg Med Chem 22: 4810-25 (2014) Article DOI: 10.1016/j.bmc.2014.06.058 BindingDB Entry DOI: 10.7270/Q2KS6T58
					More data for this Ligand-Target Pair
Glycogen phosphorylase, muscle form (Homo sapiens (Human))	BDBM50422212 (CHEMBL132462) Show SMILES CNNC(=O)[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O Show InChI InChI=1S/C8H16N2O6/c1-9-10-8(15)7-6(14)5(13)4(12)3(2-11)16-7/h3-7,9,11-14H,2H2,1H3,(H,10,15)/t3-,4-,5+,6-,7-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.78E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Alcala Curated by ChEMBL					Assay Description Inhibitory activity against rabbit muscle glycogen phosphorylase				J Med Chem 40: 4089-102 (1998) Checked by Author Article DOI: 10.1021/jm970273d BindingDB Entry DOI: 10.7270/Q2S46TGM
					More data for this Ligand-Target Pair
Glycogen phosphorylase, muscle form (Homo sapiens (Human))	BDBM50077949 (2-Aminomethyl-6-hydroxymethyl-tetrahydro-pyran-3,4...) Show SMILES NCC1OC(CO)C(O)C(O)C1O Show InChI InChI=1S/C7H15NO5/c8-1-3-5(10)7(12)6(11)4(2-9)13-3/h3-7,9-12H,1-2,8H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	1.78E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Alcala Curated by ChEMBL					Assay Description Inhibitory activity against rabbit muscle glycogen phosphorylase				J Med Chem 40: 4089-102 (1998) Checked by Author Article DOI: 10.1021/jm970273d BindingDB Entry DOI: 10.7270/Q2S46TGM
					More data for this Ligand-Target Pair
Glycogen phosphorylase, muscle form (Homo sapiens (Human))	BDBM50077949 (2-Aminomethyl-6-hydroxymethyl-tetrahydro-pyran-3,4...) Show SMILES NCC1OC(CO)C(O)C(O)C1O Show InChI InChI=1S/C7H15NO5/c8-1-3-5(10)7(12)6(11)4(2-9)13-3/h3-7,9-12H,1-2,8H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	1.78E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Alcala Curated by ChEMBL					Assay Description Inhibitory activity against rabbit muscle glycogen phosphorylase				J Med Chem 40: 4089-102 (1998) Checked by Author Article DOI: 10.1021/jm970273d BindingDB Entry DOI: 10.7270/Q2S46TGM
					More data for this Ligand-Target Pair
Glycogen phosphorylase, muscle form (Homo sapiens (Human))	BDBM50454691 (MELIBIOSE) Show SMILES OC[C@H]1O[C@H](OCC2O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]2O)[C@H](O)[C@@H](O)[C@H]1O |r| Show InChI InChI=1S/C12H22O11/c13-1-3-5(14)8(17)10(19)12(23-3)21-2-4-6(15)7(16)9(18)11(20)22-4/h3-20H,1-2H2/t3-,4?,5+,6-,7+,8+,9-,10-,11-,12+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase PC cid PC sid UniChem Similars	Article PubMed	1.79E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Alcala Curated by ChEMBL					Assay Description Inhibitory activity against rabbit muscle glycogen phosphorylase				J Med Chem 40: 4089-102 (1998) Checked by Author Article DOI: 10.1021/jm970273d BindingDB Entry DOI: 10.7270/Q2S46TGM
					More data for this Ligand-Target Pair
Glycogen phosphorylase, muscle form (Homo sapiens (Human))	BDBM50422217 (CHEMBL2303800) Show SMILES OC[C@@H]1O[C@@](O)(CO)[C@@H](O)[C@@H](O)[C@@H]1O |r| Show InChI InChI=1S/C7H14O7/c8-1-3-4(10)5(11)6(12)7(13,2-9)14-3/h3-6,8-13H,1-2H2/t3-,4+,5-,6-,7-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.80E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Alcala Curated by ChEMBL					Assay Description Inhibitory activity against rabbit muscle glycogen phosphorylase				J Med Chem 40: 4089-102 (1998) Checked by Author Article DOI: 10.1021/jm970273d BindingDB Entry DOI: 10.7270/Q2S46TGM
					More data for this Ligand-Target Pair
Glycogen phosphorylase, muscle form (Homo sapiens (Human))	BDBM50369251 (CHEMBL335028) Show SMILES OC[C@H]1O[C@@H](CN=[N+]=[N-])[C@H](O)[C@@H](O)[C@@H]1O Show InChI InChI=1S/C7H13N3O5/c8-10-9-1-3-5(12)7(14)6(13)4(2-11)15-3/h3-7,11-14H,1-2H2/t3-,4+,5-,6+,7+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.82E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Alcala Curated by ChEMBL					Assay Description Inhibitory activity against rabbit muscle glycogen phosphorylase				J Med Chem 40: 4089-102 (1998) Checked by Author Article DOI: 10.1021/jm970273d BindingDB Entry DOI: 10.7270/Q2S46TGM
					More data for this Ligand-Target Pair
Glycogen phosphorylase, muscle form (Homo sapiens (Human))	BDBM50454689 (CHEMBL336829) Show SMILES OCC1OC(OC[C@H]2O[C@H](O)C(S)[C@@H](O)[C@@H]2O)C(O)C(O)C1O Show InChI InChI=1S/C12H22O10S/c13-1-3-5(14)7(16)9(18)12(22-3)20-2-4-6(15)8(17)10(23)11(19)21-4/h3-19,23H,1-2H2/t3?,4-,5?,6-,7?,8+,9?,10?,11+,12?/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	2.00E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Alcala Curated by ChEMBL					Assay Description Inhibitory activity against rabbit muscle glycogen phosphorylase				J Med Chem 40: 4089-102 (1998) Checked by Author Article DOI: 10.1021/jm970273d BindingDB Entry DOI: 10.7270/Q2S46TGM
					More data for this Ligand-Target Pair
Glycogen phosphorylase, muscle form (Homo sapiens (Human))	BDBM50057735 ((3,4,5-Trihydroxy-6-hydroxymethyl-tetrahydro-pyran...) Show SMILES [H][C@@]1(CC#N)O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O Show InChI InChI=1S/C8H13NO5/c9-2-1-4-6(11)8(13)7(12)5(3-10)14-4/h4-8,10-13H,1,3H2/t4-,5+,6-,7+,8+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	2.04E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Alcala Curated by ChEMBL					Assay Description Inhibitory activity against rabbit muscle glycogen phosphorylase				J Med Chem 40: 4089-102 (1998) Checked by Author Article DOI: 10.1021/jm970273d BindingDB Entry DOI: 10.7270/Q2S46TGM
					More data for this Ligand-Target Pair
Glycogen phosphorylase, muscle form (Homo sapiens (Human))	BDBM50422211 (CHEMBL135465) Show SMILES OC[C@H]1O[C@@](O)(CC#N)[C@H](O)[C@@H](O)[C@@H]1O Show InChI InChI=1S/C8H13NO6/c9-2-1-8(14)7(13)6(12)5(11)4(3-10)15-8/h4-7,10-14H,1,3H2/t4-,5-,6+,7-,8+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	2.12E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Alcala Curated by ChEMBL					Assay Description Inhibitory activity against rabbit muscle glycogen phosphorylase				J Med Chem 40: 4089-102 (1998) Checked by Author Article DOI: 10.1021/jm970273d BindingDB Entry DOI: 10.7270/Q2S46TGM
					More data for this Ligand-Target Pair
Glycogen phosphorylase, muscle form (Homo sapiens (Human))	BDBM50057743 (3,4,5-Trihydroxy-6-hydroxymethyl-tetrahydro-pyran-...) Show SMILES OCC1OC(C(O)C(O)C1O)C(=O)Nc1ccccc1 Show InChI InChI=1S/C13H17NO6/c15-6-8-9(16)10(17)11(18)12(20-8)13(19)14-7-4-2-1-3-5-7/h1-5,8-12,15-18H,6H2,(H,14,19)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	2.27E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Alcala Curated by ChEMBL					Assay Description Inhibitory activity against rabbit muscle glycogen phosphorylase				J Med Chem 40: 4089-102 (1998) Checked by Author Article DOI: 10.1021/jm970273d BindingDB Entry DOI: 10.7270/Q2S46TGM
					More data for this Ligand-Target Pair
Glycogen phosphorylase, muscle form (Homo sapiens (Human))	BDBM50057752 (CHEMBL423484 | Methanesulfonic acid 3,4,5-trihydro...) Show SMILES CS(=O)(=O)OCC1OC(CO)C(O)C(O)C1O Show InChI InChI=1S/C8H16O8S/c1-17(13,14)15-3-5-7(11)8(12)6(10)4(2-9)16-5/h4-12H,2-3H2,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	2.32E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Alcala Curated by ChEMBL					Assay Description Inhibitory activity against rabbit muscle glycogen phosphorylase				J Med Chem 40: 4089-102 (1998) Checked by Author Article DOI: 10.1021/jm970273d BindingDB Entry DOI: 10.7270/Q2S46TGM
					More data for this Ligand-Target Pair
Glycogen phosphorylase, muscle form (Homo sapiens (Human))	BDBM50454692 (CHEMBL1160001) Show SMILES NCCC1OC(CO)C(O)C(O)C1O Show InChI InChI=1S/C8H17NO5/c9-2-1-4-6(11)8(13)7(12)5(3-10)14-4/h4-8,10-13H,1-3,9H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	2.35E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Alcala Curated by ChEMBL					Assay Description Inhibitory activity against rabbit muscle glycogen phosphorylase				J Med Chem 40: 4089-102 (1998) Checked by Author Article DOI: 10.1021/jm970273d BindingDB Entry DOI: 10.7270/Q2S46TGM
					More data for this Ligand-Target Pair
Glycogen phosphorylase, muscle form (Homo sapiens (Human))	BDBM50422214 (CHEMBL2303801) Show SMILES CS(=O)(=O)OC[C@]1(O)O[C@@H](CO)[C@@H](O)[C@H](O)[C@@H]1O |r| Show InChI InChI=1S/C8H16O9S/c1-18(14,15)16-3-8(13)7(12)6(11)5(10)4(2-9)17-8/h4-7,9-13H,2-3H2,1H3/t4-,5+,6-,7-,8-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	2.43E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Alcala Curated by ChEMBL					Assay Description Inhibitory activity against rabbit muscle glycogen phosphorylase				J Med Chem 40: 4089-102 (1998) Checked by Author Article DOI: 10.1021/jm970273d BindingDB Entry DOI: 10.7270/Q2S46TGM
					More data for this Ligand-Target Pair
Glycogen phosphorylase, muscle form (Homo sapiens (Human))	BDBM50057719 (3,4,5-Trihydroxy-6-hydroxymethyl-tetrahydro-pyran-...) Show SMILES [H][C@]1(O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)C(=O)NN Show InChI InChI=1S/C7H14N2O6/c8-9-7(14)6-5(13)4(12)3(11)2(1-10)15-6/h2-6,10-13H,1,8H2,(H,9,14)/t2-,3-,4+,5-,6-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	2.52E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Alcala Curated by ChEMBL					Assay Description Inhibitory activity against rabbit muscle glycogen phosphorylase				J Med Chem 40: 4089-102 (1998) Checked by Author Article DOI: 10.1021/jm970273d BindingDB Entry DOI: 10.7270/Q2S46TGM
					More data for this Ligand-Target Pair
Glycogen phosphorylase, muscle form (Homo sapiens (Human))	BDBM50057719 (3,4,5-Trihydroxy-6-hydroxymethyl-tetrahydro-pyran-...) Show SMILES [H][C@]1(O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)C(=O)NN Show InChI InChI=1S/C7H14N2O6/c8-9-7(14)6-5(13)4(12)3(11)2(1-10)15-6/h2-6,10-13H,1,8H2,(H,9,14)/t2-,3-,4+,5-,6-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	2.52E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Alcala Curated by ChEMBL					Assay Description Inhibitory activity against rabbit muscle glycogen phosphorylase				J Med Chem 40: 4089-102 (1998) Checked by Author Article DOI: 10.1021/jm970273d BindingDB Entry DOI: 10.7270/Q2S46TGM
					More data for this Ligand-Target Pair
Glycogen phosphorylase, muscle form (Homo sapiens (Human))	BDBM50057736 (3,4,5-Trihydroxy-6-hydroxymethyl-tetrahydro-pyran-...) Show SMILES COC(=O)C1OC(CO)C(O)C(O)C1O Show InChI InChI=1S/C8H14O7/c1-14-8(13)7-6(12)5(11)4(10)3(2-9)15-7/h3-7,9-12H,2H2,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	2.55E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Alcala Curated by ChEMBL					Assay Description Inhibitory activity against rabbit muscle glycogen phosphorylase				J Med Chem 40: 4089-102 (1998) Checked by Author Article DOI: 10.1021/jm970273d BindingDB Entry DOI: 10.7270/Q2S46TGM
					More data for this Ligand-Target Pair
Glycogen phosphorylase, muscle form (Homo sapiens (Human))	BDBM50057736 (3,4,5-Trihydroxy-6-hydroxymethyl-tetrahydro-pyran-...) Show SMILES COC(=O)C1OC(CO)C(O)C(O)C1O Show InChI InChI=1S/C8H14O7/c1-14-8(13)7-6(12)5(11)4(10)3(2-9)15-7/h3-7,9-12H,2H2,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	2.55E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Alcala Curated by ChEMBL					Assay Description Inhibitory activity against rabbit muscle glycogen phosphorylase				J Med Chem 40: 4089-102 (1998) Checked by Author Article DOI: 10.1021/jm970273d BindingDB Entry DOI: 10.7270/Q2S46TGM
					More data for this Ligand-Target Pair
Glycogen phosphorylase, muscle form (Homo sapiens (Human))	BDBM50057751 (3,4,5-Trihydroxy-6-hydroxymethyl-tetrahydro-pyran-...) Show SMILES OCCNC(=O)C1OC(CO)C(O)C(O)C1O Show InChI InChI=1S/C9H17NO7/c11-2-1-10-9(16)8-7(15)6(14)5(13)4(3-12)17-8/h4-8,11-15H,1-3H2,(H,10,16)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	Article PubMed	2.57E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Alcala Curated by ChEMBL					Assay Description Inhibitory activity against rabbit muscle glycogen phosphorylase				J Med Chem 40: 4089-102 (1998) Checked by Author Article DOI: 10.1021/jm970273d BindingDB Entry DOI: 10.7270/Q2S46TGM
					More data for this Ligand-Target Pair
Glycogen phosphorylase, muscle form (Homo sapiens (Human))	BDBM50454693 (CHEMBL131427) Show SMILES OC[C@H]1OC(Oc2cn(C3OC(CO)C(O)C(O)C3O)c3ccccc23)[C@H](O)[C@@H](O)[C@@H]1O Show InChI InChI=1S/C20H27NO11/c22-6-11-13(24)15(26)17(28)19(30-11)21-5-10(8-3-1-2-4-9(8)21)31-20-18(29)16(27)14(25)12(7-23)32-20/h1-5,11-20,22-29H,6-7H2/t11?,12-,13?,14-,15?,16+,17?,18-,19?,20?/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem	Article PubMed	2.57E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Alcala Curated by ChEMBL					Assay Description Inhibitory activity against rabbit muscle glycogen phosphorylase				J Med Chem 40: 4089-102 (1998) Checked by Author Article DOI: 10.1021/jm970273d BindingDB Entry DOI: 10.7270/Q2S46TGM
					More data for this Ligand-Target Pair

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