Compile Data Set for Download or QSAR

Found 919 hits Enz. Inhib. hit(s) with Target = 'Glycogen phosphorylase, muscle form'   

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 (PYGM) (Oryctolagus cuniculus (rabbit))	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 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 KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	630	-36.0	n/a	n/a	n/a	n/a	n/a	6.8	30
Universite de Lyon					Assay Description Phosphorylase activity was measured in the direction of glycogen synthesis by the release of orthophosphate from Glc-1-P. The enzyme was assayed in g...				Bioorg Med Chem 17: 7368-80 (2009) Article DOI: 10.1016/j.bmc.2009.08.060 BindingDB Entry DOI: 10.7270/Q28P5XV8
					More data for this Ligand-Target Pair				3D Structure (docked)
Glycogen Phosphorylase (PYGM) (Oryctolagus cuniculus (rabbit))	BDBM34106 (glucopyranosylidene-spiro-isoxazoline, 4a) Show SMILES COc1ccc(cc1)C1=NO[C@@]2(C1)O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O Show InChI InChI=1S/C15H19NO7/c1-21-9-4-2-8(3-5-9)10-6-15(23-16-10)14(20)13(19)12(18)11(7-17)22-15/h2-5,11-14,17-20H,6-7H2,1H3/t11-,12-,13+,14-,15-/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid PDB UniChem Similars	PDB Article PubMed	6.60E+3	-30.1	n/a	n/a	n/a	n/a	n/a	6.8	30
Universite de Lyon					Assay Description Phosphorylase activity was measured in the direction of glycogen synthesis by the release of orthophosphate from Glc-1-P. The enzyme was assayed in g...				Bioorg Med Chem 17: 7368-80 (2009) Article DOI: 10.1016/j.bmc.2009.08.060 BindingDB Entry DOI: 10.7270/Q28P5XV8
					More data for this Ligand-Target Pair				3D Structure (crystal)
Glycogen Phosphorylase (PYGM) (Oryctolagus cuniculus (rabbit))	BDBM34107 (glucopyranosylidene-spiro-isoxazoline, 4b) Show SMILES Cc1ccc(cc1)C1=NO[C@@]2(C1)O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O Show InChI InChI=1S/C15H19NO6/c1-8-2-4-9(5-3-8)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 KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	7.90E+3	-29.6	n/a	n/a	n/a	n/a	n/a	6.8	30
Universite de Lyon					Assay Description Phosphorylase activity was measured in the direction of glycogen synthesis by the release of orthophosphate from Glc-1-P. The enzyme was assayed in g...				Bioorg Med Chem 17: 7368-80 (2009) Article DOI: 10.1016/j.bmc.2009.08.060 BindingDB Entry DOI: 10.7270/Q28P5XV8
					More data for this Ligand-Target Pair				3D Structure (docked)
Glycogen Phosphorylase (PYGM) (Oryctolagus cuniculus (rabbit))	BDBM34108 (glucopyranosylidene-spiro-isoxazoline, 4c) Show SMILES OC[C@H]1O[C@@]2(CC(=NO2)c2ccccc2)[C@H](O)[C@@H](O)[C@@H]1O Show InChI InChI=1S/C14H17NO6/c16-7-10-11(17)12(18)13(19)14(20-10)6-9(15-21-14)8-4-2-1-3-5-8/h1-5,10-13,16-19H,6-7H2/t10-,11-,12+,13-,14-/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	DrugBank PC cid PC sid PDB UniChem Similars	PDB Article PubMed	1.96E+4	-27.3	n/a	n/a	n/a	n/a	n/a	6.8	30
Universite de Lyon					Assay Description Phosphorylase activity was measured in the direction of glycogen synthesis by the release of orthophosphate from Glc-1-P. The enzyme was assayed in g...				Bioorg Med Chem 17: 7368-80 (2009) Article DOI: 10.1016/j.bmc.2009.08.060 BindingDB Entry DOI: 10.7270/Q28P5XV8
					More data for this Ligand-Target Pair				3D Structure (crystal)
Glycogen Phosphorylase (PYGM) (Oryctolagus cuniculus (rabbit))	BDBM34109 (glucopyranosylidene-spiro-isoxazoline, 4d) Show SMILES OC[C@H]1O[C@@]2(CC(=NO2)c2ccc(cc2)[N+]([O-])=O)[C@H](O)[C@@H](O)[C@@H]1O Show InChI InChI=1S/C14H16N2O8/c17-6-10-11(18)12(19)13(20)14(23-10)5-9(15-24-14)7-1-3-8(4-2-7)16(21)22/h1-4,10-13,17-20H,5-6H2/t10-,11-,12+,13-,14-/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	9.25E+4	-23.4	n/a	n/a	n/a	n/a	n/a	6.8	30
Universite de Lyon					Assay Description Phosphorylase activity was measured in the direction of glycogen synthesis by the release of orthophosphate from Glc-1-P. The enzyme was assayed in g...				Bioorg Med Chem 17: 7368-80 (2009) Article DOI: 10.1016/j.bmc.2009.08.060 BindingDB Entry DOI: 10.7270/Q28P5XV8
					More data for this Ligand-Target Pair				3D Structure (docked)
Glycogen Phosphorylase (PYGM) (Oryctolagus cuniculus (rabbit))	BDBM35331 (2-oxo-1,2-dihydropyridin-3-yl amide derivative, 7t) Show SMILES Clc1ccc(CNC(=O)Cn2cccc(NCc3ccccc3)c2=O)cc1Cl Show InChI InChI=1S/C21H19Cl2N3O2/c22-17-9-8-16(11-18(17)23)13-25-20(27)14-26-10-4-7-19(21(26)28)24-12-15-5-2-1-3-6-15/h1-11,24H,12-14H2,(H,25,27)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	6.30E+3	n/a	n/a	n/a	n/a	7.2	22
Griffith University					Assay Description RMGPa (Rabbit Muscle Glycogen Phosphorylase a) activity was measured in the direction of glycogen synthesis by the formation of inorganic phosphate f...				Bioorg Med Chem 17: 4724-33 (2009) Article DOI: 10.1016/j.bmc.2009.04.049 BindingDB Entry DOI: 10.7270/Q2PR7TBG
					More data for this Ligand-Target Pair
Glycogen Phosphorylase (PYGM) (Oryctolagus cuniculus (rabbit))	BDBM35332 (2-oxo-1,2-dihydropyridin-3-yl amide derivative, 7u) Show SMILES OC[C@H](Cc1ccccc1)NC(=O)Cn1cccc(NCc2ccccc2)c1=O Show InChI InChI=1S/C23H25N3O3/c27-17-20(14-18-8-3-1-4-9-18)25-22(28)16-26-13-7-12-21(23(26)29)24-15-19-10-5-2-6-11-19/h1-13,20,24,27H,14-17H2,(H,25,28)/t20-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	n/a	n/a	n/a	7.2	22
Griffith University					Assay Description RMGPa (Rabbit Muscle Glycogen Phosphorylase a) activity was measured in the direction of glycogen synthesis by the formation of inorganic phosphate f...				Bioorg Med Chem 17: 4724-33 (2009) Article DOI: 10.1016/j.bmc.2009.04.049 BindingDB Entry DOI: 10.7270/Q2PR7TBG
					More data for this Ligand-Target Pair
Glycogen Phosphorylase (PYGM) (Oryctolagus cuniculus (rabbit))	BDBM35333 (2-oxo-1,2-dihydropyridin-3-yl amide derivative, 7v) Show SMILES OC[C@@H](NC(=O)Cn1cccc(NCc2ccccc2)c1=O)c1ccccc1 Show InChI InChI=1S/C22H23N3O3/c26-16-20(18-10-5-2-6-11-18)24-21(27)15-25-13-7-12-19(22(25)28)23-14-17-8-3-1-4-9-17/h1-13,20,23,26H,14-16H2,(H,24,27)/t20-/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.20E+5	n/a	n/a	n/a	n/a	7.2	22
Griffith University					Assay Description RMGPa (Rabbit Muscle Glycogen Phosphorylase a) activity was measured in the direction of glycogen synthesis by the formation of inorganic phosphate f...				Bioorg Med Chem 17: 4724-33 (2009) Article DOI: 10.1016/j.bmc.2009.04.049 BindingDB Entry DOI: 10.7270/Q2PR7TBG
					More data for this Ligand-Target Pair
Glycogen Phosphorylase (PYGM) (Oryctolagus cuniculus (rabbit))	BDBM35334 (2-oxo-1,2-dihydropyridin-3-yl amide derivative, 7w) Show SMILES O=C(Cn1cccc(NCc2ccccc2)c1=O)NC1CCN(Cc2ccccc2)CC1 Show InChI InChI=1S/C26H30N4O2/c31-25(28-23-13-16-29(17-14-23)19-22-10-5-2-6-11-22)20-30-15-7-12-24(26(30)32)27-18-21-8-3-1-4-9-21/h1-12,15,23,27H,13-14,16-20H2,(H,28,31)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	8.13E+5	n/a	n/a	n/a	n/a	7.2	22
Griffith University					Assay Description RMGPa (Rabbit Muscle Glycogen Phosphorylase a) activity was measured in the direction of glycogen synthesis by the formation of inorganic phosphate f...				Bioorg Med Chem 17: 4724-33 (2009) Article DOI: 10.1016/j.bmc.2009.04.049 BindingDB Entry DOI: 10.7270/Q2PR7TBG
					More data for this Ligand-Target Pair
Glycogen Phosphorylase (PYGM) (Oryctolagus cuniculus (rabbit))	BDBM35335 (2-oxo-1,2-dihydropyridin-3-yl amide derivative, 7x) Show SMILES COc1ccccc1CNC(=O)Cn1cccc(NCc2ccccc2)c1=O Show InChI InChI=1S/C22H23N3O3/c1-28-20-12-6-5-10-18(20)15-24-21(26)16-25-13-7-11-19(22(25)27)23-14-17-8-3-2-4-9-17/h2-13,23H,14-16H2,1H3,(H,24,26)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.08E+5	n/a	n/a	n/a	n/a	7.2	22
Griffith University					Assay Description RMGPa (Rabbit Muscle Glycogen Phosphorylase a) activity was measured in the direction of glycogen synthesis by the formation of inorganic phosphate f...				Bioorg Med Chem 17: 4724-33 (2009) Article DOI: 10.1016/j.bmc.2009.04.049 BindingDB Entry DOI: 10.7270/Q2PR7TBG
					More data for this Ligand-Target Pair
Glycogen Phosphorylase (PYGM) (Oryctolagus cuniculus (rabbit))	BDBM35336 (2-oxo-1,2-dihydropyridin-3-yl amide derivative, 8t) Show SMILES CC(=O)Nc1cccn(CC(=O)NCc2ccc(Cl)c(Cl)c2)c1=O Show InChI InChI=1S/C16H15Cl2N3O3/c1-10(22)20-14-3-2-6-21(16(14)24)9-15(23)19-8-11-4-5-12(17)13(18)7-11/h2-7H,8-9H2,1H3,(H,19,23)(H,20,22)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.72E+5	n/a	n/a	n/a	n/a	7.2	22
Griffith University					Assay Description RMGPa (Rabbit Muscle Glycogen Phosphorylase a) activity was measured in the direction of glycogen synthesis by the formation of inorganic phosphate f...				Bioorg Med Chem 17: 4724-33 (2009) Article DOI: 10.1016/j.bmc.2009.04.049 BindingDB Entry DOI: 10.7270/Q2PR7TBG
					More data for this Ligand-Target Pair
Glycogen Phosphorylase (PYGM) (Oryctolagus cuniculus (rabbit))	BDBM35337 (2-oxo-1,2-dihydropyridin-3-yl amide derivative, 9t) Show SMILES Clc1ccc(CNC(=O)Cn2cccc(NC(=O)c3ccccc3)c2=O)cc1Cl Show InChI InChI=1S/C21H17Cl2N3O3/c22-16-9-8-14(11-17(16)23)12-24-19(27)13-26-10-4-7-18(21(26)29)25-20(28)15-5-2-1-3-6-15/h1-11H,12-13H2,(H,24,27)(H,25,28)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.62E+5	n/a	n/a	n/a	n/a	7.2	22
Griffith University					Assay Description RMGPa (Rabbit Muscle Glycogen Phosphorylase a) activity was measured in the direction of glycogen synthesis by the formation of inorganic phosphate f...				Bioorg Med Chem 17: 4724-33 (2009) Article DOI: 10.1016/j.bmc.2009.04.049 BindingDB Entry DOI: 10.7270/Q2PR7TBG
					More data for this Ligand-Target Pair
Glycogen phosphorylase, muscle form (Oryctolagus cuniculus (rabbit))	BDBM23187 ((4aS,6aS,6bR,10S,12aR,12bR,14bS)-10-hydroxy-2,2,6a...) Show SMILES CC1(C)CC[C@@]2(CC[C@]3(C)C(=CC[C@@H]4[C@@]5(C)CC[C@H](O)C(C)(C)C5CC[C@@]34C)[C@@H]2C1)C(O)=O Show InChI InChI=1S/C30H48O3/c1-25(2)14-16-30(24(32)33)17-15-28(6)19(20(30)18-25)8-9-22-27(5)12-11-23(31)26(3,4)21(27)10-13-29(22,28)7/h8,20-23,31H,9-18H2,1-7H3,(H,32,33)/t20-,21?,22+,23-,27-,28+,29+,30-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.40E+4	n/a	n/a	n/a	n/a	7.2	22
China Pharmaceutical University					Assay Description The activity of the compounds is determined by measuring the inhibitory effect of the compounds in the direction of glycogen synthesis, the conversio...				J Med Chem 51: 3540-54 (2008) Article DOI: 10.1021/jm8000949 BindingDB Entry DOI: 10.7270/Q2WQ0233
					More data for this Ligand-Target Pair
Glycogen phosphorylase, muscle form (Oryctolagus cuniculus (rabbit))	BDBM23189 ((4aS,6aS,6bR,10R,12aR,12bR,14bS)-10-hydroxy-2,2,6a...) Show SMILES CC1(C)CC[C@@]2(CC[C@]3(C)C(=CC[C@@H]4[C@@]5(C)CC[C@@H](O)C(C)(C)C5CC[C@@]34C)[C@@H]2C1)C(O)=O Show InChI InChI=1S/C30H48O3/c1-25(2)14-16-30(24(32)33)17-15-28(6)19(20(30)18-25)8-9-22-27(5)12-11-23(31)26(3,4)21(27)10-13-29(22,28)7/h8,20-23,31H,9-18H2,1-7H3,(H,32,33)/t20-,21?,22+,23+,27-,28+,29+,30-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.10E+4	n/a	n/a	n/a	n/a	7.2	22
China Pharmaceutical University					Assay Description The activity of the compounds is determined by measuring the inhibitory effect of the compounds in the direction of glycogen synthesis, the conversio...				J Med Chem 51: 3540-54 (2008) Article DOI: 10.1021/jm8000949 BindingDB Entry DOI: 10.7270/Q2WQ0233
					More data for this Ligand-Target Pair
Glycogen phosphorylase, muscle form (Oryctolagus cuniculus (rabbit))	BDBM23190 ((4aS,6aS,6bR,10R,11R,12aR,12bR,14bS)-10,11-dihydro...) 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)C5CC[C@@]34C)[C@@H]2C1)C(O)=O 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 KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	2.80E+4	n/a	n/a	n/a	n/a	7.2	22
China Pharmaceutical University					Assay Description The activity of the compounds is determined by measuring the inhibitory effect of the compounds in the direction of glycogen synthesis, the conversio...				J Med Chem 51: 3540-54 (2008) Article DOI: 10.1021/jm8000949 BindingDB Entry DOI: 10.7270/Q2WQ0233
					More data for this Ligand-Target Pair				3D Structure (docked)
Glycogen phosphorylase, muscle form (Oryctolagus cuniculus (rabbit))	BDBM23191 ((4aS,6aS,6bR,10S,11R,12aR,12bR,14bS)-10,11-dihydro...) 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)C5CC[C@@]34C)[C@@H]2C1)C(O)=O 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 KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.44E+5	n/a	n/a	n/a	n/a	7.2	22
China Pharmaceutical University					Assay Description The activity of the compounds is determined by measuring the inhibitory effect of the compounds in the direction of glycogen synthesis, the conversio...				J Med Chem 51: 3540-54 (2008) Article DOI: 10.1021/jm8000949 BindingDB Entry DOI: 10.7270/Q2WQ0233
					More data for this Ligand-Target Pair				3D Structure (docked)
Glycogen phosphorylase, muscle form (Oryctolagus cuniculus (rabbit))	BDBM23192 ((4aS,6aS,6bR,10R,11S,12aR,12bR,14bS)-10,11-dihydro...) 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)C5CC[C@@]34C)[C@@H]2C1)C(O)=O 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 KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.40E+4	n/a	n/a	n/a	n/a	7.2	22
China Pharmaceutical University					Assay Description The activity of the compounds is determined by measuring the inhibitory effect of the compounds in the direction of glycogen synthesis, the conversio...				J Med Chem 51: 3540-54 (2008) Article DOI: 10.1021/jm8000949 BindingDB Entry DOI: 10.7270/Q2WQ0233
					More data for this Ligand-Target Pair				3D Structure (docked)
Glycogen phosphorylase, muscle form (Oryctolagus cuniculus (rabbit))	BDBM23193 ((4aS,6aS,6bR,12aR,12bR,14bS)-2,2,6a,6b,9,9,12a-hep...) Show SMILES CC1(C)CC[C@@]2(CC[C@]3(C)C(=CC[C@@H]4[C@@]5(C)CCC(=O)C(C)(C)C5CC[C@@]34C)[C@@H]2C1)C(O)=O Show InChI InChI=1S/C30H46O3/c1-25(2)14-16-30(24(32)33)17-15-28(6)19(20(30)18-25)8-9-22-27(5)12-11-23(31)26(3,4)21(27)10-13-29(22,28)7/h8,20-22H,9-18H2,1-7H3,(H,32,33)/t20-,21?,22+,27-,28+,29+,30-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.80E+4	n/a	n/a	n/a	n/a	7.2	22
China Pharmaceutical University					Assay Description The activity of the compounds is determined by measuring the inhibitory effect of the compounds in the direction of glycogen synthesis, the conversio...				J Med Chem 51: 3540-54 (2008) Article DOI: 10.1021/jm8000949 BindingDB Entry DOI: 10.7270/Q2WQ0233
					More data for this Ligand-Target Pair
Glycogen phosphorylase, muscle form (Oryctolagus cuniculus (rabbit))	BDBM23194 ((2S,3S,4S,5R,6S)-6-{[(3S,6aR,6bS,8aS,11S,12aR,14aR...) Show SMILES CC1(C)[C@H](CC[C@@]2(C)C1CC[C@]1(C)[C@@H]2C(=O)C=C2[C@@H]3C[C@](C)(CC[C@]3(C)CC[C@@]12C)C(O)=O)O[C@H]1O[C@@H]([C@@H](O)[C@H](O)[C@H]1O[C@@H]1O[C@@H]([C@@H](O)[C@H](O)[C@H]1O)C(O)=O)C(O)=O Show InChI InChI=1S/C42H62O16/c1-37(2)21-8-11-42(7)31(20(43)16-18-19-17-39(4,36(53)54)13-12-38(19,3)14-15-41(18,42)6)40(21,5)10-9-22(37)55-35-30(26(47)25(46)29(57-35)33(51)52)58-34-27(48)23(44)24(45)28(56-34)32(49)50/h16,19,21-31,34-35,44-48H,8-15,17H2,1-7H3,(H,49,50)(H,51,52)(H,53,54)/t19-,21?,22-,23-,24-,25-,26-,27+,28-,29-,30+,31+,34-,35-,38+,39-,40-,41+,42+/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	8.22E+5	n/a	n/a	n/a	n/a	7.2	22
China Pharmaceutical University					Assay Description The activity of the compounds is determined by measuring the inhibitory effect of the compounds in the direction of glycogen synthesis, the conversio...				J Med Chem 51: 3540-54 (2008) Article DOI: 10.1021/jm8000949 BindingDB Entry DOI: 10.7270/Q2WQ0233
					More data for this Ligand-Target Pair
Glycogen phosphorylase, muscle form (Oryctolagus cuniculus (rabbit))	BDBM23195 ((2S,4aS,6aS,6bR,10S,12aS,12bR,14bR)-10-hydroxy-2,4...) Show SMILES CC1(C)[C@@H](O)CC[C@@]2(C)C1CC[C@]1(C)[C@@H]2C(=O)C=C2[C@@H]3C[C@](C)(CC[C@]3(C)CC[C@@]12C)C(O)=O Show InChI InChI=1S/C30H46O4/c1-25(2)21-8-11-30(7)23(28(21,5)10-9-22(25)32)20(31)16-18-19-17-27(4,24(33)34)13-12-26(19,3)14-15-29(18,30)6/h16,19,21-23,32H,8-15,17H2,1-7H3,(H,33,34)/t19-,21?,22-,23+,26+,27-,28-,29+,30+/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	6.60E+4	n/a	n/a	n/a	n/a	7.2	22
China Pharmaceutical University					Assay Description The activity of the compounds is determined by measuring the inhibitory effect of the compounds in the direction of glycogen synthesis, the conversio...				J Med Chem 51: 3540-54 (2008) Article DOI: 10.1021/jm8000949 BindingDB Entry DOI: 10.7270/Q2WQ0233
					More data for this Ligand-Target Pair
Glycogen phosphorylase, muscle form (Oryctolagus cuniculus (rabbit))	BDBM23196 ((2S,4aS,6aS,6bR,10S,12aR,12bR,14bR)-10-hydroxy-2,4...) Show SMILES CC1(C)[C@@H](O)CC[C@@]2(C)C1CC[C@]1(C)[C@@H]2CC=C2[C@@H]3C[C@](C)(CC[C@]3(C)CC[C@@]12C)C(O)=O Show InChI InChI=1S/C30H48O3/c1-25(2)21-10-13-30(7)22(28(21,5)12-11-23(25)31)9-8-19-20-18-27(4,24(32)33)15-14-26(20,3)16-17-29(19,30)6/h8,20-23,31H,9-18H2,1-7H3,(H,32,33)/t20-,21?,22+,23-,26+,27-,28-,29+,30+/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	8.20E+4	n/a	n/a	n/a	n/a	7.2	22
China Pharmaceutical University					Assay Description The activity of the compounds is determined by measuring the inhibitory effect of the compounds in the direction of glycogen synthesis, the conversio...				J Med Chem 51: 3540-54 (2008) Article DOI: 10.1021/jm8000949 BindingDB Entry DOI: 10.7270/Q2WQ0233
					More data for this Ligand-Target Pair
Glycogen phosphorylase, muscle form (Oryctolagus cuniculus (rabbit))	BDBM23197 ((1S,2R,4aS,6aS,6bR,10S,12aR,12bR,14bS)-10-hydroxy-...) Show SMILES C[C@@H]1CC[C@@]2(CC[C@]3(C)C(=CC[C@@H]4[C@@]5(C)CC[C@H](O)C(C)(C)C5CC[C@@]34C)[C@@H]2[C@H]1C)C(O)=O Show InChI InChI=1S/C30H48O3/c1-18-10-15-30(25(32)33)17-16-28(6)20(24(30)19(18)2)8-9-22-27(5)13-12-23(31)26(3,4)21(27)11-14-29(22,28)7/h8,18-19,21-24,31H,9-17H2,1-7H3,(H,32,33)/t18-,19+,21?,22-,23+,24+,27+,28-,29-,30+/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	9.00E+3	n/a	n/a	n/a	n/a	7.2	22
China Pharmaceutical University					Assay Description The activity of the compounds is determined by measuring the inhibitory effect of the compounds in the direction of glycogen synthesis, the conversio...				J Med Chem 51: 3540-54 (2008) Article DOI: 10.1021/jm8000949 BindingDB Entry DOI: 10.7270/Q2WQ0233
					More data for this Ligand-Target Pair
Glycogen phosphorylase, muscle form (Oryctolagus cuniculus (rabbit))	BDBM23198 ((1S,2R,4aS,6aS,6bR,10R,12aR,12bR,14bS)-10-hydroxy-...) Show SMILES C[C@@H]1CC[C@@]2(CC[C@]3(C)C(=CC[C@@H]4[C@@]5(C)CC[C@@H](O)C(C)(C)C5CC[C@@]34C)[C@@H]2[C@H]1C)C(O)=O Show InChI InChI=1S/C30H48O3/c1-18-10-15-30(25(32)33)17-16-28(6)20(24(30)19(18)2)8-9-22-27(5)13-12-23(31)26(3,4)21(27)11-14-29(22,28)7/h8,18-19,21-24,31H,9-17H2,1-7H3,(H,32,33)/t18-,19+,21?,22-,23-,24+,27+,28-,29-,30+/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.90E+4	n/a	n/a	n/a	n/a	7.2	22
China Pharmaceutical University					Assay Description The activity of the compounds is determined by measuring the inhibitory effect of the compounds in the direction of glycogen synthesis, the conversio...				J Med Chem 51: 3540-54 (2008) Article DOI: 10.1021/jm8000949 BindingDB Entry DOI: 10.7270/Q2WQ0233
					More data for this Ligand-Target Pair
Glycogen phosphorylase, muscle form (Oryctolagus cuniculus (rabbit))	BDBM23199 ((1S,2R,4aS,6aS,6bR,10R,11R,12aR,12bR,14bS)-10,11-d...) 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)C5CC[C@@]34C)[C@@H]2[C@H]1C)C(O)=O 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 KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	2.00E+4	n/a	n/a	n/a	n/a	7.2	22
China Pharmaceutical University					Assay Description The activity of the compounds is determined by measuring the inhibitory effect of the compounds in the direction of glycogen synthesis, the conversio...				J Med Chem 51: 3540-54 (2008) Article DOI: 10.1021/jm8000949 BindingDB Entry DOI: 10.7270/Q2WQ0233
					More data for this Ligand-Target Pair				3D Structure (docked)
Glycogen phosphorylase, muscle form (Oryctolagus cuniculus (rabbit))	BDBM23200 ((1S,2R,4aS,6aS,6bR,10S,11R,12aR,12bR,14bS)-10,11-d...) 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)C5CC[C@@]34C)[C@@H]2[C@H]1C)C(O)=O 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 KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	2.13E+5	n/a	n/a	n/a	n/a	7.2	22
China Pharmaceutical University					Assay Description The activity of the compounds is determined by measuring the inhibitory effect of the compounds in the direction of glycogen synthesis, the conversio...				J Med Chem 51: 3540-54 (2008) Article DOI: 10.1021/jm8000949 BindingDB Entry DOI: 10.7270/Q2WQ0233
					More data for this Ligand-Target Pair				3D Structure (docked)
Glycogen phosphorylase, muscle form (Oryctolagus cuniculus (rabbit))	BDBM23201 ((1S,2R,4aS,6aS,6bR,10R,11S,12aR,12bR,14bS)-10,11-d...) 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)C5CC[C@@]34C)[C@@H]2[C@H]1C)C(O)=O 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 KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.16E+5	n/a	n/a	n/a	n/a	7.2	22
China Pharmaceutical University					Assay Description The activity of the compounds is determined by measuring the inhibitory effect of the compounds in the direction of glycogen synthesis, the conversio...				J Med Chem 51: 3540-54 (2008) Article DOI: 10.1021/jm8000949 BindingDB Entry DOI: 10.7270/Q2WQ0233
					More data for this Ligand-Target Pair				3D Structure (docked)
Glycogen phosphorylase, muscle form (Oryctolagus cuniculus (rabbit))	BDBM23202 ((1S,2R,4aS,6aS,6bR,9R,10R,11R,12aR,12bR,14bS)-10,1...) 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)(CO)C5CC[C@@]34C)[C@@H]2[C@H]1C)C(O)=O Show InChI InChI=1S/C30H48O5/c1-17-9-12-30(25(34)35)14-13-28(5)19(23(30)18(17)2)7-8-22-26(3)15-20(32)24(33)27(4,16-31)21(26)10-11-29(22,28)6/h7,17-18,20-24,31-33H,8-16H2,1-6H3,(H,34,35)/t17-,18+,20-,21?,22-,23+,24+,26+,27+,28-,29-,30+/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.70E+4	n/a	n/a	n/a	n/a	7.2	22
China Pharmaceutical University					Assay Description The activity of the compounds is determined by measuring the inhibitory effect of the compounds in the direction of glycogen synthesis, the conversio...				J Med Chem 51: 3540-54 (2008) Article DOI: 10.1021/jm8000949 BindingDB Entry DOI: 10.7270/Q2WQ0233
					More data for this Ligand-Target Pair				3D Structure (docked)
Glycogen phosphorylase, muscle form (Oryctolagus cuniculus (rabbit))	BDBM23203 ((1S,2R,4aS,6aS,6bR,12aR,12bR,14bS)-1,2,6a,6b,9,9,1...) Show SMILES C[C@@H]1CC[C@@]2(CC[C@]3(C)C(=CC[C@@H]4[C@@]5(C)CCC(=O)C(C)(C)C5CC[C@@]34C)[C@@H]2[C@H]1C)C(O)=O Show InChI InChI=1S/C30H46O3/c1-18-10-15-30(25(32)33)17-16-28(6)20(24(30)19(18)2)8-9-22-27(5)13-12-23(31)26(3,4)21(27)11-14-29(22,28)7/h8,18-19,21-22,24H,9-17H2,1-7H3,(H,32,33)/t18-,19+,21?,22-,24+,27+,28-,29-,30+/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5.70E+4	n/a	n/a	n/a	n/a	7.2	22
China Pharmaceutical University					Assay Description The activity of the compounds is determined by measuring the inhibitory effect of the compounds in the direction of glycogen synthesis, the conversio...				J Med Chem 51: 3540-54 (2008) Article DOI: 10.1021/jm8000949 BindingDB Entry DOI: 10.7270/Q2WQ0233
					More data for this Ligand-Target Pair
Glycogen phosphorylase, muscle form (Oryctolagus cuniculus (rabbit))	BDBM23204 ((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl...) Show SMILES CC1(C)CC[C@@]2(CC[C@]3(C)C(=CC[C@@H]4[C@@]5(C)CC[C@H](O)C(C)(C)C5CC[C@@]34C)[C@@H]2C1)C(=O)O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O Show InChI InChI=1S/C36H58O8/c1-31(2)14-16-36(30(42)44-29-28(41)27(40)26(39)22(19-37)43-29)17-15-34(6)20(21(36)18-31)8-9-24-33(5)12-11-25(38)32(3,4)23(33)10-13-35(24,34)7/h8,21-29,37-41H,9-19H2,1-7H3/t21-,22+,23?,24+,25-,26+,27-,28+,29-,33-,34+,35+,36-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.93E+5	n/a	n/a	n/a	n/a	7.2	22
China Pharmaceutical University					Assay Description The activity of the compounds is determined by measuring the inhibitory effect of the compounds in the direction of glycogen synthesis, the conversio...				J Med Chem 51: 3540-54 (2008) Article DOI: 10.1021/jm8000949 BindingDB Entry DOI: 10.7270/Q2WQ0233
					More data for this Ligand-Target Pair
Glycogen phosphorylase, muscle form (Oryctolagus cuniculus (rabbit))	BDBM23205 ((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl...) Show SMILES C[C@@H]1CC[C@@]2(CC[C@]3(C)C(=CC[C@@H]4[C@@]5(C)CC[C@H](O)C(C)(C)C5CC[C@@]34C)[C@@H]2[C@H]1C)C(=O)O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O Show InChI InChI=1S/C36H58O8/c1-19-10-15-36(31(42)44-30-29(41)28(40)27(39)22(18-37)43-30)17-16-34(6)21(26(36)20(19)2)8-9-24-33(5)13-12-25(38)32(3,4)23(33)11-14-35(24,34)7/h8,19-20,22-30,37-41H,9-18H2,1-7H3/t19-,20+,22-,23?,24-,25+,26+,27-,28+,29-,30+,33+,34-,35-,36+/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	9.70E+4	n/a	n/a	n/a	n/a	7.2	22
China Pharmaceutical University					Assay Description The activity of the compounds is determined by measuring the inhibitory effect of the compounds in the direction of glycogen synthesis, the conversio...				J Med Chem 51: 3540-54 (2008) Article DOI: 10.1021/jm8000949 BindingDB Entry DOI: 10.7270/Q2WQ0233
					More data for this Ligand-Target Pair
Glycogen phosphorylase, muscle form (Oryctolagus cuniculus (rabbit))	BDBM23206 ((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl...) 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)C5CC[C@@]34C)[C@@H]2[C@H]1C)C(=O)O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O Show InChI InChI=1S/C36H58O9/c1-18-10-13-36(31(43)45-30-28(41)27(40)26(39)22(17-37)44-30)15-14-34(6)20(25(36)19(18)2)8-9-24-33(5)16-21(38)29(42)32(3,4)23(33)11-12-35(24,34)7/h8,18-19,21-30,37-42H,9-17H2,1-7H3/t18-,19+,21-,22-,23?,24-,25+,26-,27+,28-,29+,30+,33+,34-,35-,36+/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.06E+5	n/a	n/a	n/a	n/a	7.2	22
China Pharmaceutical University					Assay Description The activity of the compounds is determined by measuring the inhibitory effect of the compounds in the direction of glycogen synthesis, the conversio...				J Med Chem 51: 3540-54 (2008) Article DOI: 10.1021/jm8000949 BindingDB Entry DOI: 10.7270/Q2WQ0233
					More data for this Ligand-Target Pair
Glycogen phosphorylase, muscle form (Oryctolagus cuniculus (rabbit))	BDBM23207 ((1R,2R,5S,8R,9R,10R,13R,14R,17S,19R)-5-(hydroxymet...) Show SMILES CC(=C)[C@@H]1CC[C@]2(CO)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC[C@H](O)C(C)(C)[C@@H]5CC[C@@]34C)[C@@H]12 Show InChI InChI=1S/C30H50O2/c1-19(2)20-10-15-30(18-31)17-16-28(6)21(25(20)30)8-9-23-27(5)13-12-24(32)26(3,4)22(27)11-14-29(23,28)7/h20-25,31-32H,1,8-18H2,2-7H3/t20-,21+,22-,23+,24-,25+,27-,28+,29+,30+/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase KEGG PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	1.70E+4	n/a	n/a	n/a	n/a	7.2	22
China Pharmaceutical University					Assay Description The activity of the compounds is determined by measuring the inhibitory effect of the compounds in the direction of glycogen synthesis, the conversio...				J Med Chem 51: 3540-54 (2008) Article DOI: 10.1021/jm8000949 BindingDB Entry DOI: 10.7270/Q2WQ0233
					More data for this Ligand-Target Pair
Glycogen phosphorylase, muscle form (Oryctolagus cuniculus (rabbit))	BDBM23208 ((1R,2R,5S,8R,9R,10R,13R,14R,17S,19R)-17-hydroxy-1,...) Show SMILES CC(=C)[C@@H]1CC[C@@]2(CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC[C@H](O)C(C)(C)[C@@H]5CC[C@@]34C)[C@@H]12)C(O)=O Show InChI InChI=1S/C30H48O3/c1-18(2)19-10-15-30(25(32)33)17-16-28(6)20(24(19)30)8-9-22-27(5)13-12-23(31)26(3,4)21(27)11-14-29(22,28)7/h19-24,31H,1,8-17H2,2-7H3,(H,32,33)/t19-,20+,21-,22+,23-,24+,27-,28+,29+,30-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase CHEMBL KEGG PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	4.30E+4	n/a	n/a	n/a	n/a	7.2	22
China Pharmaceutical University					Assay Description The activity of the compounds is determined by measuring the inhibitory effect of the compounds in the direction of glycogen synthesis, the conversio...				J Med Chem 51: 3540-54 (2008) Article DOI: 10.1021/jm8000949 BindingDB Entry DOI: 10.7270/Q2WQ0233
					More data for this Ligand-Target Pair
Glycogen phosphorylase, muscle form (Oryctolagus cuniculus (rabbit))	BDBM23209 ((1R,2R,5S,8R,9R,10R,13R,14R,17S,18R,19R)-17-hydrox...) Show SMILES CC(=C)[C@@H]1CC[C@@]2(CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC[C@H](O)[C@@](C)(CO)[C@@H]5CC[C@@]34C)[C@@H]12)C(O)=O Show InChI InChI=1S/C30H48O4/c1-18(2)19-9-14-30(25(33)34)16-15-28(5)20(24(19)30)7-8-22-26(3)12-11-23(32)27(4,17-31)21(26)10-13-29(22,28)6/h19-24,31-32H,1,7-17H2,2-6H3,(H,33,34)/t19-,20+,21+,22+,23-,24+,26-,27-,28+,29+,30-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	1.60E+4	n/a	n/a	n/a	n/a	7.2	22
China Pharmaceutical University					Assay Description The activity of the compounds is determined by measuring the inhibitory effect of the compounds in the direction of glycogen synthesis, the conversio...				J Med Chem 51: 3540-54 (2008) Article DOI: 10.1021/jm8000949 BindingDB Entry DOI: 10.7270/Q2WQ0233
					More data for this Ligand-Target Pair
Glycogen phosphorylase, muscle form (Oryctolagus cuniculus (rabbit))	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 KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase CHEMBL DrugBank KEGG MMDB PC cid PC sid PDB UniChem Patents Similars	PDB Article PubMed	n/a	n/a	1.14E+5	n/a	n/a	n/a	n/a	7.2	22
China Pharmaceutical University					Assay Description The activity of the compounds is determined by measuring the inhibitory effect of the compounds in the direction of glycogen synthesis, the conversio...				J Med Chem 51: 3540-54 (2008) Article DOI: 10.1021/jm8000949 BindingDB Entry DOI: 10.7270/Q2WQ0233
					More data for this Ligand-Target Pair				3D Structure (crystal)
Glycogen phosphorylase, muscle form (Oryctolagus cuniculus (rabbit))	BDBM23210 ((1S,2R,4aS,6aS,6bR,8R,9R,10R,11R,12aR,12bR,14bS)-8...) 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)(CO)C5[C@H](O)C[C@@]34C)[C@@H]2[C@H]1C)C(O)=O Show InChI InChI=1S/C30H48O6/c1-16-9-10-30(25(35)36)12-11-28(5)18(22(30)17(16)2)7-8-21-26(3)13-20(33)24(34)27(4,15-31)23(26)19(32)14-29(21,28)6/h7,16-17,19-24,31-34H,8-15H2,1-6H3,(H,35,36)/t16-,17+,19-,20-,21-,22+,23?,24+,26-,27+,28-,29-,30+/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	n/a	n/a	n/a	7.2	22
China Pharmaceutical University					Assay Description The activity of the compounds is determined by measuring the inhibitory effect of the compounds in the direction of glycogen synthesis, the conversio...				J Med Chem 51: 3540-54 (2008) Article DOI: 10.1021/jm8000949 BindingDB Entry DOI: 10.7270/Q2WQ0233
					More data for this Ligand-Target Pair
Glycogen phosphorylase, muscle form (Oryctolagus cuniculus (rabbit))	BDBM23211 ((2S,3R,4S,5S,6R)-6-({[(2R,3R,4R,5S,6R)-3,4-dihydro...) 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)(CO)[C@@H]5CC[C@@]34C)[C@@H]2[C@H]1C)C(=O)O[C@@H]1O[C@H](CO[C@@H]2O[C@H](CO)[C@@H](O[C@@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@@H](O)[C@H](O)[C@H]1O Show InChI InChI=1S/C48H78O19/c1-20-10-13-48(15-14-46(6)23(29(48)21(20)2)8-9-28-44(4)16-24(51)39(60)45(5,19-50)27(44)11-12-47(28,46)7)43(61)67-42-36(58)33(55)31(53)26(65-42)18-62-40-37(59)34(56)38(25(17-49)64-40)66-41-35(57)32(54)30(52)22(3)63-41/h8,20-22,24-42,49-60H,9-19H2,1-7H3/t20-,21+,22+,24-,25-,26-,27-,28-,29+,30+,31-,32-,33+,34-,35-,36-,37-,38-,39+,40-,41+,42+,44+,45+,46-,47-,48+/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase KEGG PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	n/a	n/a	n/a	7.2	22
China Pharmaceutical University					Assay Description The activity of the compounds is determined by measuring the inhibitory effect of the compounds in the direction of glycogen synthesis, the conversio...				J Med Chem 51: 3540-54 (2008) Article DOI: 10.1021/jm8000949 BindingDB Entry DOI: 10.7270/Q2WQ0233
					More data for this Ligand-Target Pair
Glycogen phosphorylase, muscle form (Oryctolagus cuniculus (rabbit))	BDBM23212 ((2S,3R,4S,5S,6R)-6-({[(2R,3R,4R,5S,6R)-3,4-dihydro...) 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)(CO)[C@@H]5[C@H](O)C[C@@]34C)[C@@H]2[C@H]1C)C(=O)O[C@@H]1O[C@H](CO[C@@H]2O[C@H](CO)[C@@H](O[C@@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@@H](O)[C@H](O)[C@H]1O Show InChI InChI=1S/C48H78O20/c1-19-10-11-48(13-12-46(6)22(28(48)20(19)2)8-9-27-44(4)14-24(52)39(61)45(5,18-50)38(44)23(51)15-47(27,46)7)43(62)68-42-35(59)32(56)30(54)26(66-42)17-63-40-36(60)33(57)37(25(16-49)65-40)67-41-34(58)31(55)29(53)21(3)64-41/h8,19-21,23-42,49-61H,9-18H2,1-7H3/t19-,20+,21+,23-,24-,25-,26-,27-,28+,29+,30-,31-,32+,33-,34-,35-,36-,37-,38-,39+,40-,41+,42+,44-,45+,46-,47-,48+/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	n/a	n/a	n/a	7.2	22
China Pharmaceutical University					Assay Description The activity of the compounds is determined by measuring the inhibitory effect of the compounds in the direction of glycogen synthesis, the conversio...				J Med Chem 51: 3540-54 (2008) Article DOI: 10.1021/jm8000949 BindingDB Entry DOI: 10.7270/Q2WQ0233
					More data for this Ligand-Target Pair
Glycogen Phosphorylase (PYGM) (Oryctolagus cuniculus (rabbit))	BDBM34071 (benzamide derivative, 6) Show SMILES Cn1ccnc1Sc1cc(C(=O)Nc2nccs2)c(N)cc1F Show InChI InChI=1S/C14H12FN5OS2/c1-20-4-2-18-14(20)23-11-6-8(10(16)7-9(11)15)12(21)19-13-17-3-5-22-13/h2-7H,16H2,1H3,(H,17,19,21)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase DrugBank MMDB PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	4.39E+4	n/a	n/a	n/a	n/a	7.2	22
Shanghai Institutes for Biological Sciences					Assay Description The enzymatic inhibition of phosphorylase activity was monitored using microplate reader (Bio-Rad). In brief, GPa activity was measured in the direct...				Bioorg Med Chem 17: 7301-12 (2009) Article DOI: 10.1016/j.bmc.2009.08.045 BindingDB Entry DOI: 10.7270/Q2DF6PK0
					More data for this Ligand-Target Pair
Glycogen Phosphorylase (PYGM) (Oryctolagus cuniculus (rabbit))	BDBM34072 (benzamide derivative, 12) Show SMILES Cn1ccnc1Sc1cc(C(=O)Nc2cccc(N)c2)c(N)cc1F Show InChI InChI=1S/C17H16FN5OS/c1-23-6-5-21-17(23)25-15-8-12(14(20)9-13(15)18)16(24)22-11-4-2-3-10(19)7-11/h2-9H,19-20H2,1H3,(H,22,24)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.68E+3	n/a	n/a	n/a	n/a	7.2	22
Shanghai Institutes for Biological Sciences					Assay Description The enzymatic inhibition of phosphorylase activity was monitored using microplate reader (Bio-Rad). In brief, GPa activity was measured in the direct...				Bioorg Med Chem 17: 7301-12 (2009) Article DOI: 10.1016/j.bmc.2009.08.045 BindingDB Entry DOI: 10.7270/Q2DF6PK0
					More data for this Ligand-Target Pair
Glycogen Phosphorylase (PYGM) (Oryctolagus cuniculus (rabbit))	BDBM34073 (benzamide derivative, 13a) Show SMILES Nc1cccc(NC(=O)c2cc(Sc3nccs3)c(F)cc2N)c1 Show InChI InChI=1S/C16H13FN4OS2/c17-12-8-13(19)11(7-14(12)24-16-20-4-5-23-16)15(22)21-10-3-1-2-9(18)6-10/h1-8H,18-19H2,(H,21,22)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5.40E+3	n/a	n/a	n/a	n/a	7.2	22
Shanghai Institutes for Biological Sciences					Assay Description The enzymatic inhibition of phosphorylase activity was monitored using microplate reader (Bio-Rad). In brief, GPa activity was measured in the direct...				Bioorg Med Chem 17: 7301-12 (2009) Article DOI: 10.1016/j.bmc.2009.08.045 BindingDB Entry DOI: 10.7270/Q2DF6PK0
					More data for this Ligand-Target Pair
Glycogen Phosphorylase (PYGM) (Oryctolagus cuniculus (rabbit))	BDBM34074 (benzamide derivative, 13b) Show SMILES Cc1csc(Sc2cc(C(=O)Nc3cccc(N)c3)c(N)cc2F)n1 Show InChI InChI=1S/C17H15FN4OS2/c1-9-8-24-17(21-9)25-15-6-12(14(20)7-13(15)18)16(23)22-11-4-2-3-10(19)5-11/h2-8H,19-20H2,1H3,(H,22,23)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.50E+3	n/a	n/a	n/a	n/a	7.2	22
Shanghai Institutes for Biological Sciences					Assay Description The enzymatic inhibition of phosphorylase activity was monitored using microplate reader (Bio-Rad). In brief, GPa activity was measured in the direct...				Bioorg Med Chem 17: 7301-12 (2009) Article DOI: 10.1016/j.bmc.2009.08.045 BindingDB Entry DOI: 10.7270/Q2DF6PK0
					More data for this Ligand-Target Pair
Glycogen Phosphorylase (PYGM) (Oryctolagus cuniculus (rabbit))	BDBM34075 (benzamide derivative, 13c) Show SMILES Nc1cccc(NC(=O)c2cc(Sc3nncs3)c(F)cc2N)c1 Show InChI InChI=1S/C15H12FN5OS2/c16-11-6-12(18)10(5-13(11)24-15-21-19-7-23-15)14(22)20-9-3-1-2-8(17)4-9/h1-7H,17-18H2,(H,20,22)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.77E+4	n/a	n/a	n/a	n/a	7.2	22
Shanghai Institutes for Biological Sciences					Assay Description The enzymatic inhibition of phosphorylase activity was monitored using microplate reader (Bio-Rad). In brief, GPa activity was measured in the direct...				Bioorg Med Chem 17: 7301-12 (2009) Article DOI: 10.1016/j.bmc.2009.08.045 BindingDB Entry DOI: 10.7270/Q2DF6PK0
					More data for this Ligand-Target Pair
Glycogen Phosphorylase (PYGM) (Oryctolagus cuniculus (rabbit))	BDBM34076 (benzamide derivative, 13d) Show SMILES Nc1cccc(NC(=O)c2cc(Sc3ccccn3)c(F)cc2N)c1 Show InChI InChI=1S/C18H15FN4OS/c19-14-10-15(21)13(9-16(14)25-17-6-1-2-7-22-17)18(24)23-12-5-3-4-11(20)8-12/h1-10H,20-21H2,(H,23,24)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.06E+4	n/a	n/a	n/a	n/a	7.2	22
Shanghai Institutes for Biological Sciences					Assay Description The enzymatic inhibition of phosphorylase activity was monitored using microplate reader (Bio-Rad). In brief, GPa activity was measured in the direct...				Bioorg Med Chem 17: 7301-12 (2009) Article DOI: 10.1016/j.bmc.2009.08.045 BindingDB Entry DOI: 10.7270/Q2DF6PK0
					More data for this Ligand-Target Pair
Glycogen Phosphorylase (PYGM) (Oryctolagus cuniculus (rabbit))	BDBM34077 (benzamide derivative, 13e) Show SMILES Cc1cc(C)nc(Sc2cc(C(=O)Nc3cccc(N)c3)c(N)cc2F)n1 Show InChI InChI=1S/C19H18FN5OS/c1-10-6-11(2)24-19(23-10)27-17-8-14(16(22)9-15(17)20)18(26)25-13-5-3-4-12(21)7-13/h3-9H,21-22H2,1-2H3,(H,25,26)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	9.80E+3	n/a	n/a	n/a	n/a	7.2	22
Shanghai Institutes for Biological Sciences					Assay Description The enzymatic inhibition of phosphorylase activity was monitored using microplate reader (Bio-Rad). In brief, GPa activity was measured in the direct...				Bioorg Med Chem 17: 7301-12 (2009) Article DOI: 10.1016/j.bmc.2009.08.045 BindingDB Entry DOI: 10.7270/Q2DF6PK0
					More data for this Ligand-Target Pair
Glycogen Phosphorylase (PYGM) (Oryctolagus cuniculus (rabbit))	BDBM34078 (benzamide derivative, 13f) Show SMILES Cn1ccnc1Sc1cc(NC(=O)c2cccc(N)c2)c(N)cc1F Show InChI InChI=1S/C17H16FN5OS/c1-23-6-5-21-17(23)25-15-9-14(13(20)8-12(15)18)22-16(24)10-3-2-4-11(19)7-10/h2-9H,19-20H2,1H3,(H,22,24)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.89E+4	n/a	n/a	n/a	n/a	7.2	22
Shanghai Institutes for Biological Sciences					Assay Description The enzymatic inhibition of phosphorylase activity was monitored using microplate reader (Bio-Rad). In brief, GPa activity was measured in the direct...				Bioorg Med Chem 17: 7301-12 (2009) Article DOI: 10.1016/j.bmc.2009.08.045 BindingDB Entry DOI: 10.7270/Q2DF6PK0
					More data for this Ligand-Target Pair
Glycogen Phosphorylase (PYGM) (Oryctolagus cuniculus (rabbit))	BDBM34079 (benzamide derivative, 13g) Show SMILES Cn1ccnc1Sc1cc(C(=O)Nc2cccc(CN)c2)c(N)cc1F Show InChI InChI=1S/C18H18FN5OS/c1-24-6-5-22-18(24)26-16-8-13(15(21)9-14(16)19)17(25)23-12-4-2-3-11(7-12)10-20/h2-9H,10,20-21H2,1H3,(H,23,25)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.53E+4	n/a	n/a	n/a	n/a	7.2	22
Shanghai Institutes for Biological Sciences					Assay Description The enzymatic inhibition of phosphorylase activity was monitored using microplate reader (Bio-Rad). In brief, GPa activity was measured in the direct...				Bioorg Med Chem 17: 7301-12 (2009) Article DOI: 10.1016/j.bmc.2009.08.045 BindingDB Entry DOI: 10.7270/Q2DF6PK0
					More data for this Ligand-Target Pair
Glycogen Phosphorylase (PYGM) (Oryctolagus cuniculus (rabbit))	BDBM34080 (benzamide derivative, 13h) Show SMILES Cn1ccnc1Sc1cc(C(=O)Nc2cccc(c2)C(F)(F)F)c(N)cc1F Show InChI InChI=1S/C18H14F4N4OS/c1-26-6-5-24-17(26)28-15-8-12(14(23)9-13(15)19)16(27)25-11-4-2-3-10(7-11)18(20,21)22/h2-9H,23H2,1H3,(H,25,27)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	8.95E+3	n/a	n/a	n/a	n/a	7.2	22
Shanghai Institutes for Biological Sciences					Assay Description The enzymatic inhibition of phosphorylase activity was monitored using microplate reader (Bio-Rad). In brief, GPa activity was measured in the direct...				Bioorg Med Chem 17: 7301-12 (2009) Article DOI: 10.1016/j.bmc.2009.08.045 BindingDB Entry DOI: 10.7270/Q2DF6PK0
					More data for this Ligand-Target Pair
Glycogen Phosphorylase (PYGM) (Oryctolagus cuniculus (rabbit))	BDBM34081 (benzamide derivative, 13i) Show SMILES Nc1cc(F)c(Sc2nccs2)cc1C(=O)Nc1cccc(c1)C(F)(F)F Show InChI InChI=1S/C17H11F4N3OS2/c18-12-8-13(22)11(7-14(12)27-16-23-4-5-26-16)15(25)24-10-3-1-2-9(6-10)17(19,20)21/h1-8H,22H2,(H,24,25)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.11E+4	n/a	n/a	n/a	n/a	7.2	22
Shanghai Institutes for Biological Sciences					Assay Description The enzymatic inhibition of phosphorylase activity was monitored using microplate reader (Bio-Rad). In brief, GPa activity was measured in the direct...				Bioorg Med Chem 17: 7301-12 (2009) Article DOI: 10.1016/j.bmc.2009.08.045 BindingDB Entry DOI: 10.7270/Q2DF6PK0
					More data for this Ligand-Target Pair
Glycogen Phosphorylase (PYGM) (Oryctolagus cuniculus (rabbit))	BDBM34082 (benzamide derivative, 13j) Show SMILES Cc1csc(Sc2cc(C(=O)Nc3cccc(c3)C(F)(F)F)c(N)cc2F)n1 Show InChI InChI=1S/C18H13F4N3OS2/c1-9-8-27-17(24-9)28-15-6-12(14(23)7-13(15)19)16(26)25-11-4-2-3-10(5-11)18(20,21)22/h2-8H,23H2,1H3,(H,25,26)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.25E+4	n/a	n/a	n/a	n/a	7.2	22
Shanghai Institutes for Biological Sciences					Assay Description The enzymatic inhibition of phosphorylase activity was monitored using microplate reader (Bio-Rad). In brief, GPa activity was measured in the direct...				Bioorg Med Chem 17: 7301-12 (2009) Article DOI: 10.1016/j.bmc.2009.08.045 BindingDB Entry DOI: 10.7270/Q2DF6PK0
					More data for this Ligand-Target Pair

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