Compile Data Set for Download or QSAR

Found 85 hits Enz. Inhib. hit(s) with all data for entry = 50016849   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kJ/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Glycogen phosphorylase, liver form (Homo sapiens (Human))	BDBM50174389 (1-(2-Chloro-4-fluoro-benzoyl)-3-(5-hydroxy-2-metho...) Show SMILES COc1ccc(O)cc1NC(=O)NC(=O)c1ccc(F)cc1Cl Show InChI InChI=1S/C15H12ClFN2O4/c1-23-13-5-3-9(20)7-12(13)18-15(22)19-14(21)10-4-2-8(17)6-11(10)16/h2-7,20H,1H3,(H2,18,19,21,22)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL DrugBank MMDB PC cid PC sid PDB UniChem Similars	MMDB PDB Article PubMed	n/a	n/a	22.9	n/a	n/a	n/a	n/a	7.2	n/a
Sanofi-Aventis Deutschland GmbH Curated by ChEMBL					Assay Description Logarithmic inhibitory concentration against human liver glycogen phosphorylase enzyme by the addition of glucose-1-phosphate and incubated for 40 mi...				J Med Chem 48: 6178-93 (2005) Article DOI: 10.1021/jm049034y BindingDB Entry DOI: 10.7270/Q2FT8KJ5
					More data for this Ligand-Target Pair				3D Structure (crystal)
Glycogen phosphorylase, liver form (Homo sapiens (Human))	BDBM50174389 (1-(2-Chloro-4-fluoro-benzoyl)-3-(5-hydroxy-2-metho...) Show SMILES COc1ccc(O)cc1NC(=O)NC(=O)c1ccc(F)cc1Cl Show InChI InChI=1S/C15H12ClFN2O4/c1-23-13-5-3-9(20)7-12(13)18-15(22)19-14(21)10-4-2-8(17)6-11(10)16/h2-7,20H,1H3,(H2,18,19,21,22)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL DrugBank MMDB PC cid PC sid PDB UniChem Similars	MMDB PDB Article PubMed	n/a	n/a	23	n/a	n/a	n/a	n/a	7.2	n/a
Sanofi-Aventis Deutschland GmbH Curated by ChEMBL					Assay Description Inhibitory concentration against human liver glycogen phosphorylase enzyme by the addition of glucose-1-phosphate upon incubating for 40 min at 25 de...				J Med Chem 48: 6178-93 (2005) Article DOI: 10.1021/jm049034y BindingDB Entry DOI: 10.7270/Q2FT8KJ5
					More data for this Ligand-Target Pair				3D Structure (crystal)
Glycogen phosphorylase, liver form (Homo sapiens (Human))	BDBM50174381 (4-[3-(2-Chloro-4,5-difluoro-benzoyl)-ureido]-2-hyd...) Show SMILES COc1cc(C(O)=O)c(O)cc1NC(=O)NC(=O)c1cc(F)c(F)cc1Cl Show InChI InChI=1S/C16H11ClF2N2O6/c1-27-13-3-7(15(24)25)12(22)5-11(13)20-16(26)21-14(23)6-2-9(18)10(19)4-8(6)17/h2-5,22H,1H3,(H,24,25)(H2,20,21,23,26)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	50	n/a	n/a	n/a	n/a	7.2	n/a
Sanofi-Aventis Deutschland GmbH Curated by ChEMBL					Assay Description Inhibitory concentration against human liver glycogen phosphorylase enzyme by the addition of glucose-1-phosphate upon incubating for 40 min at 25 de...				J Med Chem 48: 6178-93 (2005) Article DOI: 10.1021/jm049034y BindingDB Entry DOI: 10.7270/Q2FT8KJ5
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Homo sapiens (Human))	BDBM50174381 (4-[3-(2-Chloro-4,5-difluoro-benzoyl)-ureido]-2-hyd...) Show SMILES COc1cc(C(O)=O)c(O)cc1NC(=O)NC(=O)c1cc(F)c(F)cc1Cl Show InChI InChI=1S/C16H11ClF2N2O6/c1-27-13-3-7(15(24)25)12(22)5-11(13)20-16(26)21-14(23)6-2-9(18)10(19)4-8(6)17/h2-5,22H,1H3,(H,24,25)(H2,20,21,23,26)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	50.1	n/a	n/a	n/a	n/a	7.2	n/a
Sanofi-Aventis Deutschland GmbH Curated by ChEMBL					Assay Description Logarithmic inhibitory concentration against human liver glycogen phosphorylase enzyme by the addition of glucose-1-phosphate and incubated for 40 mi...				J Med Chem 48: 6178-93 (2005) Article DOI: 10.1021/jm049034y BindingDB Entry DOI: 10.7270/Q2FT8KJ5
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Homo sapiens (Human))	BDBM50174379 (1-{3-[3-(2-Chloro-4,5-difluoro-benzoyl)-ureido]-4-...) Show SMILES CNC(=O)Nc1ccc(OC)c(NC(=O)NC(=O)c2cc(F)c(F)cc2Cl)c1 Show InChI InChI=1S/C17H15ClF2N4O4/c1-21-16(26)22-8-3-4-14(28-2)13(5-8)23-17(27)24-15(25)9-6-11(19)12(20)7-10(9)18/h3-7H,1-2H3,(H2,21,22,26)(H2,23,24,25,27)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	52.5	n/a	n/a	n/a	n/a	7.2	n/a
Sanofi-Aventis Deutschland GmbH Curated by ChEMBL					Assay Description Logarithmic inhibitory concentration against human liver glycogen phosphorylase enzyme by the addition of glucose-1-phosphate and incubated for 40 mi...				J Med Chem 48: 6178-93 (2005) Article DOI: 10.1021/jm049034y BindingDB Entry DOI: 10.7270/Q2FT8KJ5
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Homo sapiens (Human))	BDBM50174379 (1-{3-[3-(2-Chloro-4,5-difluoro-benzoyl)-ureido]-4-...) Show SMILES CNC(=O)Nc1ccc(OC)c(NC(=O)NC(=O)c2cc(F)c(F)cc2Cl)c1 Show InChI InChI=1S/C17H15ClF2N4O4/c1-21-16(26)22-8-3-4-14(28-2)13(5-8)23-17(27)24-15(25)9-6-11(19)12(20)7-10(9)18/h3-7H,1-2H3,(H2,21,22,26)(H2,23,24,25,27)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	53	n/a	n/a	n/a	n/a	7.2	n/a
Sanofi-Aventis Deutschland GmbH Curated by ChEMBL					Assay Description Inhibitory concentration against human liver glycogen phosphorylase enzyme by the addition of glucose-1-phosphate upon incubating for 40 min at 25 de...				J Med Chem 48: 6178-93 (2005) Article DOI: 10.1021/jm049034y BindingDB Entry DOI: 10.7270/Q2FT8KJ5
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Homo sapiens (Human))	BDBM50174397 (CHEMBL370848 | N-{4-Chloro-3-[3-(2-chloro-4,5-difl...) Show SMILES CC(=O)Nc1ccc(Cl)c(NC(=O)NC(=O)c2cc(F)c(F)cc2Cl)c1 Show InChI InChI=1S/C16H11Cl2F2N3O3/c1-7(24)21-8-2-3-10(17)14(4-8)22-16(26)23-15(25)9-5-12(19)13(20)6-11(9)18/h2-6H,1H3,(H,21,24)(H2,22,23,25,26)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	60	n/a	n/a	n/a	n/a	7.2	n/a
Sanofi-Aventis Deutschland GmbH Curated by ChEMBL					Assay Description Inhibitory concentration against human liver glycogen phosphorylase enzyme by the addition of glucose-1-phosphate upon incubating for 40 min at 25 de...				J Med Chem 48: 6178-93 (2005) Article DOI: 10.1021/jm049034y BindingDB Entry DOI: 10.7270/Q2FT8KJ5
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Homo sapiens (Human))	BDBM50174375 (CHEMBL381870 | N-{3-[3-(2-Chloro-4,5-difluoro-benz...) Show SMILES COc1ccc(NC(C)=O)cc1NC(=O)NC(=O)c1cc(F)c(F)cc1Cl Show InChI InChI=1S/C17H14ClF2N3O4/c1-8(24)21-9-3-4-15(27-2)14(5-9)22-17(26)23-16(25)10-6-12(19)13(20)7-11(10)18/h3-7H,1-2H3,(H,21,24)(H2,22,23,25,26)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	60	n/a	n/a	n/a	n/a	7.2	n/a
Sanofi-Aventis Deutschland GmbH Curated by ChEMBL					Assay Description Inhibitory concentration against human liver glycogen phosphorylase enzyme by the addition of glucose-1-phosphate upon incubating for 40 min at 25 de...				J Med Chem 48: 6178-93 (2005) Article DOI: 10.1021/jm049034y BindingDB Entry DOI: 10.7270/Q2FT8KJ5
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Homo sapiens (Human))	BDBM50174375 (CHEMBL381870 | N-{3-[3-(2-Chloro-4,5-difluoro-benz...) Show SMILES COc1ccc(NC(C)=O)cc1NC(=O)NC(=O)c1cc(F)c(F)cc1Cl Show InChI InChI=1S/C17H14ClF2N3O4/c1-8(24)21-9-3-4-15(27-2)14(5-9)22-17(26)23-16(25)10-6-12(19)13(20)7-11(10)18/h3-7H,1-2H3,(H,21,24)(H2,22,23,25,26)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	60.3	n/a	n/a	n/a	n/a	7.2	n/a
Sanofi-Aventis Deutschland GmbH Curated by ChEMBL					Assay Description Logarithmic inhibitory concentration against human liver glycogen phosphorylase enzyme by the addition of glucose-1-phosphate and incubated for 40 mi...				J Med Chem 48: 6178-93 (2005) Article DOI: 10.1021/jm049034y BindingDB Entry DOI: 10.7270/Q2FT8KJ5
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Homo sapiens (Human))	BDBM50174397 (CHEMBL370848 | N-{4-Chloro-3-[3-(2-chloro-4,5-difl...) Show SMILES CC(=O)Nc1ccc(Cl)c(NC(=O)NC(=O)c2cc(F)c(F)cc2Cl)c1 Show InChI InChI=1S/C16H11Cl2F2N3O3/c1-7(24)21-8-2-3-10(17)14(4-8)22-16(26)23-15(25)9-5-12(19)13(20)6-11(9)18/h2-6H,1H3,(H,21,24)(H2,22,23,25,26)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	60.3	n/a	n/a	n/a	n/a	7.2	n/a
Sanofi-Aventis Deutschland GmbH Curated by ChEMBL					Assay Description Logarithmic inhibitory concentration against human liver glycogen phosphorylase enzyme by the addition of glucose-1-phosphate and incubated for 40 mi...				J Med Chem 48: 6178-93 (2005) Article DOI: 10.1021/jm049034y BindingDB Entry DOI: 10.7270/Q2FT8KJ5
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Homo sapiens (Human))	BDBM50174372 (1-(2-Chloro-benzoyl)-3-(5-hydroxy-2-methoxy-phenyl...) Show SMILES COc1ccc(O)cc1NC(=O)NC(=O)c1ccccc1Cl Show InChI InChI=1S/C15H13ClN2O4/c1-22-13-7-6-9(19)8-12(13)17-15(21)18-14(20)10-4-2-3-5-11(10)16/h2-8,19H,1H3,(H2,17,18,20,21)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	64.6	n/a	n/a	n/a	n/a	7.2	n/a
Sanofi-Aventis Deutschland GmbH Curated by ChEMBL					Assay Description Logarithmic inhibitory concentration against human liver glycogen phosphorylase enzyme by the addition of glucose-1-phosphate and incubated for 40 mi...				J Med Chem 48: 6178-93 (2005) Article DOI: 10.1021/jm049034y BindingDB Entry DOI: 10.7270/Q2FT8KJ5
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Homo sapiens (Human))	BDBM50174372 (1-(2-Chloro-benzoyl)-3-(5-hydroxy-2-methoxy-phenyl...) Show SMILES COc1ccc(O)cc1NC(=O)NC(=O)c1ccccc1Cl Show InChI InChI=1S/C15H13ClN2O4/c1-22-13-7-6-9(19)8-12(13)17-15(21)18-14(20)10-4-2-3-5-11(10)16/h2-8,19H,1H3,(H2,17,18,20,21)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	65	n/a	n/a	n/a	n/a	7.2	n/a
Sanofi-Aventis Deutschland GmbH Curated by ChEMBL					Assay Description Inhibitory concentration against human liver glycogen phosphorylase enzyme by the addition of glucose-1-phosphate upon incubating for 40 min at 25 de...				J Med Chem 48: 6178-93 (2005) Article DOI: 10.1021/jm049034y BindingDB Entry DOI: 10.7270/Q2FT8KJ5
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Homo sapiens (Human))	BDBM50174366 (1-(2-Chloro-4-fluoro-benzoyl)-3-[4-(1H-tetrazol-5-...) Show SMILES Fc1ccc(C(=O)NC(=O)Nc2ccc(cc2OC(F)(F)F)-c2nnn[nH]2)c(Cl)c1 Show InChI InChI=1S/C16H9ClF4N6O3/c17-10-6-8(18)2-3-9(10)14(28)23-15(29)22-11-4-1-7(13-24-26-27-25-13)5-12(11)30-16(19,20)21/h1-6H,(H2,22,23,28,29)(H,24,25,26,27)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	79.4	n/a	n/a	n/a	n/a	7.2	n/a
Sanofi-Aventis Deutschland GmbH Curated by ChEMBL					Assay Description Logarithmic inhibitory concentration against human liver glycogen phosphorylase enzyme by the addition of glucose-1-phosphate and incubated for 40 mi...				J Med Chem 48: 6178-93 (2005) Article DOI: 10.1021/jm049034y BindingDB Entry DOI: 10.7270/Q2FT8KJ5
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Homo sapiens (Human))	BDBM50174366 (1-(2-Chloro-4-fluoro-benzoyl)-3-[4-(1H-tetrazol-5-...) Show SMILES Fc1ccc(C(=O)NC(=O)Nc2ccc(cc2OC(F)(F)F)-c2nnn[nH]2)c(Cl)c1 Show InChI InChI=1S/C16H9ClF4N6O3/c17-10-6-8(18)2-3-9(10)14(28)23-15(29)22-11-4-1-7(13-24-26-27-25-13)5-12(11)30-16(19,20)21/h1-6H,(H2,22,23,28,29)(H,24,25,26,27)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	80	n/a	n/a	n/a	n/a	7.2	n/a
Sanofi-Aventis Deutschland GmbH Curated by ChEMBL					Assay Description Inhibitory concentration against human liver glycogen phosphorylase enzyme by the addition of glucose-1-phosphate upon incubating for 40 min at 25 de...				J Med Chem 48: 6178-93 (2005) Article DOI: 10.1021/jm049034y BindingDB Entry DOI: 10.7270/Q2FT8KJ5
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Homo sapiens (Human))	BDBM50174384 (5-Chloro-4-[3-(2-chloro-4,5-difluoro-benzoyl)-urei...) Show SMILES OC(=O)c1cc(Cl)c(NC(=O)NC(=O)c2cc(F)c(F)cc2Cl)cc1O Show InChI InChI=1S/C15H8Cl2F2N2O5/c16-7-3-10(19)9(18)2-5(7)13(23)21-15(26)20-11-4-12(22)6(14(24)25)1-8(11)17/h1-4,22H,(H,24,25)(H2,20,21,23,26)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	89.1	n/a	n/a	n/a	n/a	7.2	n/a
Sanofi-Aventis Deutschland GmbH Curated by ChEMBL					Assay Description Logarithmic inhibitory concentration against human liver glycogen phosphorylase enzyme by the addition of glucose-1-phosphate and incubated for 40 mi...				J Med Chem 48: 6178-93 (2005) Article DOI: 10.1021/jm049034y BindingDB Entry DOI: 10.7270/Q2FT8KJ5
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Homo sapiens (Human))	BDBM50174384 (5-Chloro-4-[3-(2-chloro-4,5-difluoro-benzoyl)-urei...) Show SMILES OC(=O)c1cc(Cl)c(NC(=O)NC(=O)c2cc(F)c(F)cc2Cl)cc1O Show InChI InChI=1S/C15H8Cl2F2N2O5/c16-7-3-10(19)9(18)2-5(7)13(23)21-15(26)20-11-4-12(22)6(14(24)25)1-8(11)17/h1-4,22H,(H,24,25)(H2,20,21,23,26)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	90	n/a	n/a	n/a	n/a	7.2	n/a
Sanofi-Aventis Deutschland GmbH Curated by ChEMBL					Assay Description Inhibitory concentration against human liver glycogen phosphorylase enzyme by the addition of glucose-1-phosphate upon incubating for 40 min at 25 de...				J Med Chem 48: 6178-93 (2005) Article DOI: 10.1021/jm049034y BindingDB Entry DOI: 10.7270/Q2FT8KJ5
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Homo sapiens (Human))	BDBM50174378 (1-(2-Chloro-4-fluoro-benzoyl)-3-(3,4-dihydroxy-phe...) Show SMILES Oc1ccc(NC(=O)NC(=O)c2ccc(F)cc2Cl)cc1O Show InChI InChI=1S/C14H10ClFN2O4/c15-10-5-7(16)1-3-9(10)13(21)18-14(22)17-8-2-4-11(19)12(20)6-8/h1-6,19-20H,(H2,17,18,21,22)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	120	n/a	n/a	n/a	n/a	7.2	n/a
Sanofi-Aventis Deutschland GmbH Curated by ChEMBL					Assay Description Inhibitory concentration against human liver glycogen phosphorylase enzyme by the addition of glucose-1-phosphate upon incubating for 40 min at 25 de...				J Med Chem 48: 6178-93 (2005) Article DOI: 10.1021/jm049034y BindingDB Entry DOI: 10.7270/Q2FT8KJ5
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Homo sapiens (Human))	BDBM50174378 (1-(2-Chloro-4-fluoro-benzoyl)-3-(3,4-dihydroxy-phe...) Show SMILES Oc1ccc(NC(=O)NC(=O)c2ccc(F)cc2Cl)cc1O Show InChI InChI=1S/C14H10ClFN2O4/c15-10-5-7(16)1-3-9(10)13(21)18-14(22)17-8-2-4-11(19)12(20)6-8/h1-6,19-20H,(H2,17,18,21,22)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	120	n/a	n/a	n/a	n/a	7.2	n/a
Sanofi-Aventis Deutschland GmbH Curated by ChEMBL					Assay Description Logarithmic inhibitory concentration against human liver glycogen phosphorylase enzyme by the addition of glucose-1-phosphate and incubated for 40 mi...				J Med Chem 48: 6178-93 (2005) Article DOI: 10.1021/jm049034y BindingDB Entry DOI: 10.7270/Q2FT8KJ5
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Homo sapiens (Human))	BDBM50174405 (4-[3-(2-Chloro-4-fluoro-benzoyl)-ureido]-3-trifluo...) Show SMILES OC(=O)c1ccc(NC(=O)NC(=O)c2ccc(F)cc2Cl)c(OC(F)(F)F)c1 Show InChI InChI=1S/C16H9ClF4N2O5/c17-10-6-8(18)2-3-9(10)13(24)23-15(27)22-11-4-1-7(14(25)26)5-12(11)28-16(19,20)21/h1-6H,(H,25,26)(H2,22,23,24,27)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	150	n/a	n/a	n/a	n/a	7.2	n/a
Sanofi-Aventis Deutschland GmbH Curated by ChEMBL					Assay Description Inhibitory concentration against human liver glycogen phosphorylase enzyme by the addition of glucose-1-phosphate upon incubating for 40 min at 25 de...				J Med Chem 48: 6178-93 (2005) Article DOI: 10.1021/jm049034y BindingDB Entry DOI: 10.7270/Q2FT8KJ5
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Homo sapiens (Human))	BDBM50174373 (5-Chloro-4-[3-(2,4-dichloro-benzoyl)-ureido]-2-hyd...) Show SMILES OC(=O)c1cc(Cl)c(NC(=O)NC(=O)c2ccc(Cl)cc2Cl)cc1O Show InChI InChI=1S/C15H9Cl3N2O5/c16-6-1-2-7(9(17)3-6)13(22)20-15(25)19-11-5-12(21)8(14(23)24)4-10(11)18/h1-5,21H,(H,23,24)(H2,19,20,22,25)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	150	n/a	n/a	n/a	n/a	7.2	n/a
Sanofi-Aventis Deutschland GmbH Curated by ChEMBL					Assay Description Inhibitory concentration against human liver glycogen phosphorylase enzyme by the addition of glucose-1-phosphate upon incubating for 40 min at 25 de...				J Med Chem 48: 6178-93 (2005) Article DOI: 10.1021/jm049034y BindingDB Entry DOI: 10.7270/Q2FT8KJ5
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Homo sapiens (Human))	BDBM50174373 (5-Chloro-4-[3-(2,4-dichloro-benzoyl)-ureido]-2-hyd...) Show SMILES OC(=O)c1cc(Cl)c(NC(=O)NC(=O)c2ccc(Cl)cc2Cl)cc1O Show InChI InChI=1S/C15H9Cl3N2O5/c16-6-1-2-7(9(17)3-6)13(22)20-15(25)19-11-5-12(21)8(14(23)24)4-10(11)18/h1-5,21H,(H,23,24)(H2,19,20,22,25)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	151	n/a	n/a	n/a	n/a	7.2	n/a
Sanofi-Aventis Deutschland GmbH Curated by ChEMBL					Assay Description Logarithmic inhibitory concentration against human liver glycogen phosphorylase enzyme by the addition of glucose-1-phosphate and incubated for 40 mi...				J Med Chem 48: 6178-93 (2005) Article DOI: 10.1021/jm049034y BindingDB Entry DOI: 10.7270/Q2FT8KJ5
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Homo sapiens (Human))	BDBM50174405 (4-[3-(2-Chloro-4-fluoro-benzoyl)-ureido]-3-trifluo...) Show SMILES OC(=O)c1ccc(NC(=O)NC(=O)c2ccc(F)cc2Cl)c(OC(F)(F)F)c1 Show InChI InChI=1S/C16H9ClF4N2O5/c17-10-6-8(18)2-3-9(10)13(24)23-15(27)22-11-4-1-7(14(25)26)5-12(11)28-16(19,20)21/h1-6H,(H,25,26)(H2,22,23,24,27)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	151	n/a	n/a	n/a	n/a	7.2	n/a
Sanofi-Aventis Deutschland GmbH Curated by ChEMBL					Assay Description Logarithmic inhibitory concentration against human liver glycogen phosphorylase enzyme by the addition of glucose-1-phosphate and incubated for 40 mi...				J Med Chem 48: 6178-93 (2005) Article DOI: 10.1021/jm049034y BindingDB Entry DOI: 10.7270/Q2FT8KJ5
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Homo sapiens (Human))	BDBM50174374 (3-Chloro-4-[3-(2-chloro-4-fluoro-benzoyl)-ureido]-...) Show SMILES OC(=O)c1ccc(NC(=O)NC(=O)c2ccc(F)cc2Cl)c(Cl)c1 Show InChI InChI=1S/C15H9Cl2FN2O4/c16-10-6-8(18)2-3-9(10)13(21)20-15(24)19-12-4-1-7(14(22)23)5-11(12)17/h1-6H,(H,22,23)(H2,19,20,21,24)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	158	n/a	n/a	n/a	n/a	7.2	n/a
Sanofi-Aventis Deutschland GmbH Curated by ChEMBL					Assay Description Logarithmic inhibitory concentration against human liver glycogen phosphorylase enzyme by the addition of glucose-1-phosphate and incubated for 40 mi...				J Med Chem 48: 6178-93 (2005) Article DOI: 10.1021/jm049034y BindingDB Entry DOI: 10.7270/Q2FT8KJ5
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Homo sapiens (Human))	BDBM50174403 (1-{4-Chloro-3-[3-(2,4-dichloro-benzoyl)-ureido]-ph...) Show SMILES CNC(=O)Nc1ccc(Cl)c(NC(=O)NC(=O)c2ccc(Cl)cc2Cl)c1 Show InChI InChI=1S/C16H13Cl3N4O3/c1-20-15(25)21-9-3-5-11(18)13(7-9)22-16(26)23-14(24)10-4-2-8(17)6-12(10)19/h2-7H,1H3,(H2,20,21,25)(H2,22,23,24,26)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	158	n/a	n/a	n/a	n/a	7.2	n/a
Sanofi-Aventis Deutschland GmbH Curated by ChEMBL					Assay Description Logarithmic inhibitory concentration against human liver glycogen phosphorylase enzyme by the addition of glucose-1-phosphate and incubated for 40 mi...				J Med Chem 48: 6178-93 (2005) Article DOI: 10.1021/jm049034y BindingDB Entry DOI: 10.7270/Q2FT8KJ5
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Homo sapiens (Human))	BDBM50174362 (4-[3-(2-Chloro-4-fluoro-benzoyl)-ureido]-2-hydroxy...) Show SMILES COc1cc(C(O)=O)c(O)cc1NC(=O)NC(=O)c1ccc(F)cc1Cl Show InChI InChI=1S/C16H12ClFN2O6/c1-26-13-5-9(15(23)24)12(21)6-11(13)19-16(25)20-14(22)8-3-2-7(18)4-10(8)17/h2-6,21H,1H3,(H,23,24)(H2,19,20,22,25)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	158	n/a	n/a	n/a	n/a	7.2	n/a
Sanofi-Aventis Deutschland GmbH Curated by ChEMBL					Assay Description Logarithmic inhibitory concentration against human liver glycogen phosphorylase enzyme by the addition of glucose-1-phosphate and incubated for 40 mi...				J Med Chem 48: 6178-93 (2005) Article DOI: 10.1021/jm049034y BindingDB Entry DOI: 10.7270/Q2FT8KJ5
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Homo sapiens (Human))	BDBM50174362 (4-[3-(2-Chloro-4-fluoro-benzoyl)-ureido]-2-hydroxy...) Show SMILES COc1cc(C(O)=O)c(O)cc1NC(=O)NC(=O)c1ccc(F)cc1Cl Show InChI InChI=1S/C16H12ClFN2O6/c1-26-13-5-9(15(23)24)12(21)6-11(13)19-16(25)20-14(22)8-3-2-7(18)4-10(8)17/h2-6,21H,1H3,(H,23,24)(H2,19,20,22,25)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	160	n/a	n/a	n/a	n/a	7.2	n/a
Sanofi-Aventis Deutschland GmbH Curated by ChEMBL					Assay Description Inhibitory concentration against human liver glycogen phosphorylase enzyme by the addition of glucose-1-phosphate upon incubating for 40 min at 25 de...				J Med Chem 48: 6178-93 (2005) Article DOI: 10.1021/jm049034y BindingDB Entry DOI: 10.7270/Q2FT8KJ5
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Homo sapiens (Human))	BDBM50174374 (3-Chloro-4-[3-(2-chloro-4-fluoro-benzoyl)-ureido]-...) Show SMILES OC(=O)c1ccc(NC(=O)NC(=O)c2ccc(F)cc2Cl)c(Cl)c1 Show InChI InChI=1S/C15H9Cl2FN2O4/c16-10-6-8(18)2-3-9(10)13(21)20-15(24)19-12-4-1-7(14(22)23)5-11(12)17/h1-6H,(H,22,23)(H2,19,20,21,24)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	160	n/a	n/a	n/a	n/a	7.2	n/a
Sanofi-Aventis Deutschland GmbH Curated by ChEMBL					Assay Description Inhibitory concentration against human liver glycogen phosphorylase enzyme by the addition of glucose-1-phosphate upon incubating for 40 min at 25 de...				J Med Chem 48: 6178-93 (2005) Article DOI: 10.1021/jm049034y BindingDB Entry DOI: 10.7270/Q2FT8KJ5
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Homo sapiens (Human))	BDBM50174403 (1-{4-Chloro-3-[3-(2,4-dichloro-benzoyl)-ureido]-ph...) Show SMILES CNC(=O)Nc1ccc(Cl)c(NC(=O)NC(=O)c2ccc(Cl)cc2Cl)c1 Show InChI InChI=1S/C16H13Cl3N4O3/c1-20-15(25)21-9-3-5-11(18)13(7-9)22-16(26)23-14(24)10-4-2-8(17)6-12(10)19/h2-7H,1H3,(H2,20,21,25)(H2,22,23,24,26)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	160	n/a	n/a	n/a	n/a	7.2	n/a
Sanofi-Aventis Deutschland GmbH Curated by ChEMBL					Assay Description Inhibitory concentration against human liver glycogen phosphorylase enzyme by the addition of glucose-1-phosphate upon incubating for 40 min at 25 de...				J Med Chem 48: 6178-93 (2005) Article DOI: 10.1021/jm049034y BindingDB Entry DOI: 10.7270/Q2FT8KJ5
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Homo sapiens (Human))	BDBM50174368 (1-(2-Chloro-4-fluoro-benzoyl)-3-[2-chloro-4-(1H-te...) Show SMILES Fc1ccc(C(=O)NC(=O)Nc2ccc(cc2Cl)-c2nnn[nH]2)c(Cl)c1 Show InChI InChI=1S/C15H9Cl2FN6O2/c16-10-6-8(18)2-3-9(10)14(25)20-15(26)19-12-4-1-7(5-11(12)17)13-21-23-24-22-13/h1-6H,(H2,19,20,25,26)(H,21,22,23,24)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	190	n/a	n/a	n/a	n/a	7.2	n/a
Sanofi-Aventis Deutschland GmbH Curated by ChEMBL					Assay Description Inhibitory concentration against human liver glycogen phosphorylase enzyme by the addition of glucose-1-phosphate upon incubating for 40 min at 25 de...				J Med Chem 48: 6178-93 (2005) Article DOI: 10.1021/jm049034y BindingDB Entry DOI: 10.7270/Q2FT8KJ5
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Homo sapiens (Human))	BDBM50174368 (1-(2-Chloro-4-fluoro-benzoyl)-3-[2-chloro-4-(1H-te...) Show SMILES Fc1ccc(C(=O)NC(=O)Nc2ccc(cc2Cl)-c2nnn[nH]2)c(Cl)c1 Show InChI InChI=1S/C15H9Cl2FN6O2/c16-10-6-8(18)2-3-9(10)14(25)20-15(26)19-12-4-1-7(5-11(12)17)13-21-23-24-22-13/h1-6H,(H2,19,20,25,26)(H,21,22,23,24)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	191	n/a	n/a	n/a	n/a	7.2	n/a
Sanofi-Aventis Deutschland GmbH Curated by ChEMBL					Assay Description Logarithmic inhibitory concentration against human liver glycogen phosphorylase enzyme by the addition of glucose-1-phosphate and incubated for 40 mi...				J Med Chem 48: 6178-93 (2005) Article DOI: 10.1021/jm049034y BindingDB Entry DOI: 10.7270/Q2FT8KJ5
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Homo sapiens (Human))	BDBM50174380 (4-Chloro-3-[3-(2,4-dichloro-benzoyl)-ureido]-N-met...) Show SMILES CNC(=O)c1ccc(Cl)c(NC(=O)NC(=O)c2ccc(Cl)cc2Cl)c1 Show InChI InChI=1S/C16H12Cl3N3O3/c1-20-14(23)8-2-5-11(18)13(6-8)21-16(25)22-15(24)10-4-3-9(17)7-12(10)19/h2-7H,1H3,(H,20,23)(H2,21,22,24,25)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	200	n/a	n/a	n/a	n/a	7.2	n/a
Sanofi-Aventis Deutschland GmbH Curated by ChEMBL					Assay Description Logarithmic inhibitory concentration against human liver glycogen phosphorylase enzyme by the addition of glucose-1-phosphate and incubated for 40 mi...				J Med Chem 48: 6178-93 (2005) Article DOI: 10.1021/jm049034y BindingDB Entry DOI: 10.7270/Q2FT8KJ5
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Homo sapiens (Human))	BDBM50174380 (4-Chloro-3-[3-(2,4-dichloro-benzoyl)-ureido]-N-met...) Show SMILES CNC(=O)c1ccc(Cl)c(NC(=O)NC(=O)c2ccc(Cl)cc2Cl)c1 Show InChI InChI=1S/C16H12Cl3N3O3/c1-20-14(23)8-2-5-11(18)13(6-8)21-16(25)22-15(24)10-4-3-9(17)7-12(10)19/h2-7H,1H3,(H,20,23)(H2,21,22,24,25)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	200	n/a	n/a	n/a	n/a	7.2	n/a
Sanofi-Aventis Deutschland GmbH Curated by ChEMBL					Assay Description Inhibitory concentration against human liver glycogen phosphorylase enzyme by the addition of glucose-1-phosphate upon incubating for 40 min at 25 de...				J Med Chem 48: 6178-93 (2005) Article DOI: 10.1021/jm049034y BindingDB Entry DOI: 10.7270/Q2FT8KJ5
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Homo sapiens (Human))	BDBM50174388 (4-[3-(2-Chloro-4-fluoro-benzoyl)-ureido]-3-methoxy...) Show SMILES COc1cc(ccc1NC(=O)NC(=O)c1ccc(F)cc1Cl)C(O)=O Show InChI InChI=1S/C16H12ClFN2O5/c1-25-13-6-8(15(22)23)2-5-12(13)19-16(24)20-14(21)10-4-3-9(18)7-11(10)17/h2-7H,1H3,(H,22,23)(H2,19,20,21,24)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	209	n/a	n/a	n/a	n/a	7.2	n/a
Sanofi-Aventis Deutschland GmbH Curated by ChEMBL					Assay Description Logarithmic inhibitory concentration against human liver glycogen phosphorylase enzyme by the addition of glucose-1-phosphate and incubated for 40 mi...				J Med Chem 48: 6178-93 (2005) Article DOI: 10.1021/jm049034y BindingDB Entry DOI: 10.7270/Q2FT8KJ5
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Homo sapiens (Human))	BDBM50174388 (4-[3-(2-Chloro-4-fluoro-benzoyl)-ureido]-3-methoxy...) Show SMILES COc1cc(ccc1NC(=O)NC(=O)c1ccc(F)cc1Cl)C(O)=O Show InChI InChI=1S/C16H12ClFN2O5/c1-25-13-6-8(15(22)23)2-5-12(13)19-16(24)20-14(21)10-4-3-9(18)7-11(10)17/h2-7H,1H3,(H,22,23)(H2,19,20,21,24)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	210	n/a	n/a	n/a	n/a	7.2	n/a
Sanofi-Aventis Deutschland GmbH Curated by ChEMBL					Assay Description Inhibitory concentration against human liver glycogen phosphorylase enzyme by the addition of glucose-1-phosphate upon incubating for 40 min at 25 de...				J Med Chem 48: 6178-93 (2005) Article DOI: 10.1021/jm049034y BindingDB Entry DOI: 10.7270/Q2FT8KJ5
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Homo sapiens (Human))	BDBM50174369 (1-(2-Chloro-4,5-difluoro-benzoyl)-3-[2-methoxy-4-(...) Show SMILES COc1cc(ccc1NC(=O)NC(=O)c1cc(F)c(F)cc1Cl)-c1nnc(C)[nH]1 Show InChI InChI=1S/C18H14ClF2N5O3/c1-8-22-16(26-25-8)9-3-4-14(15(5-9)29-2)23-18(28)24-17(27)10-6-12(20)13(21)7-11(10)19/h3-7H,1-2H3,(H,22,25,26)(H2,23,24,27,28)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	250	n/a	n/a	n/a	n/a	7.2	n/a
Sanofi-Aventis Deutschland GmbH Curated by ChEMBL					Assay Description Inhibitory concentration against human liver glycogen phosphorylase enzyme by the addition of glucose-1-phosphate upon incubating for 40 min at 25 de...				J Med Chem 48: 6178-93 (2005) Article DOI: 10.1021/jm049034y BindingDB Entry DOI: 10.7270/Q2FT8KJ5
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Homo sapiens (Human))	BDBM50174369 (1-(2-Chloro-4,5-difluoro-benzoyl)-3-[2-methoxy-4-(...) Show SMILES COc1cc(ccc1NC(=O)NC(=O)c1cc(F)c(F)cc1Cl)-c1nnc(C)[nH]1 Show InChI InChI=1S/C18H14ClF2N5O3/c1-8-22-16(26-25-8)9-3-4-14(15(5-9)29-2)23-18(28)24-17(27)10-6-12(20)13(21)7-11(10)19/h3-7H,1-2H3,(H,22,25,26)(H2,23,24,27,28)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	251	n/a	n/a	n/a	n/a	7.2	n/a
Sanofi-Aventis Deutschland GmbH Curated by ChEMBL					Assay Description Logarithmic inhibitory concentration against human liver glycogen phosphorylase enzyme by the addition of glucose-1-phosphate and incubated for 40 mi...				J Med Chem 48: 6178-93 (2005) Article DOI: 10.1021/jm049034y BindingDB Entry DOI: 10.7270/Q2FT8KJ5
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Homo sapiens (Human))	BDBM50174395 (4-[3-(2-Chloro-4-fluoro-benzoyl)-ureido]-3-methoxy...) Show SMILES COc1cc(ccc1NC(=O)NC(=O)c1ccc(F)cc1Cl)C(N)=O Show InChI InChI=1S/C16H13ClFN3O4/c1-25-13-6-8(14(19)22)2-5-12(13)20-16(24)21-15(23)10-4-3-9(18)7-11(10)17/h2-7H,1H3,(H2,19,22)(H2,20,21,23,24)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	300	n/a	n/a	n/a	n/a	7.2	n/a
Sanofi-Aventis Deutschland GmbH Curated by ChEMBL					Assay Description Inhibitory concentration against human liver glycogen phosphorylase enzyme by the addition of glucose-1-phosphate upon incubating for 40 min at 25 de...				J Med Chem 48: 6178-93 (2005) Article DOI: 10.1021/jm049034y BindingDB Entry DOI: 10.7270/Q2FT8KJ5
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Homo sapiens (Human))	BDBM50174385 (3-[3-(2,4-Dichloro-benzoyl)-ureido]-4-methoxy-N-me...) Show SMILES CNC(=O)c1ccc(OC)c(NC(=O)NC(=O)c2ccc(Cl)cc2Cl)c1 Show InChI InChI=1S/C17H15Cl2N3O4/c1-20-15(23)9-3-6-14(26-2)13(7-9)21-17(25)22-16(24)11-5-4-10(18)8-12(11)19/h3-8H,1-2H3,(H,20,23)(H2,21,22,24,25)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	300	n/a	n/a	n/a	n/a	7.2	n/a
Sanofi-Aventis Deutschland GmbH Curated by ChEMBL					Assay Description Inhibitory concentration against human liver glycogen phosphorylase enzyme by the addition of glucose-1-phosphate upon incubating for 40 min at 25 de...				J Med Chem 48: 6178-93 (2005) Article DOI: 10.1021/jm049034y BindingDB Entry DOI: 10.7270/Q2FT8KJ5
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Homo sapiens (Human))	BDBM50174395 (4-[3-(2-Chloro-4-fluoro-benzoyl)-ureido]-3-methoxy...) Show SMILES COc1cc(ccc1NC(=O)NC(=O)c1ccc(F)cc1Cl)C(N)=O Show InChI InChI=1S/C16H13ClFN3O4/c1-25-13-6-8(14(19)22)2-5-12(13)20-16(24)21-15(23)10-4-3-9(18)7-11(10)17/h2-7H,1H3,(H2,19,22)(H2,20,21,23,24)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	302	n/a	n/a	n/a	n/a	7.2	n/a
Sanofi-Aventis Deutschland GmbH Curated by ChEMBL					Assay Description Logarithmic inhibitory concentration against human liver glycogen phosphorylase enzyme by the addition of glucose-1-phosphate and incubated for 40 mi...				J Med Chem 48: 6178-93 (2005) Article DOI: 10.1021/jm049034y BindingDB Entry DOI: 10.7270/Q2FT8KJ5
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Homo sapiens (Human))	BDBM50174385 (3-[3-(2,4-Dichloro-benzoyl)-ureido]-4-methoxy-N-me...) Show SMILES CNC(=O)c1ccc(OC)c(NC(=O)NC(=O)c2ccc(Cl)cc2Cl)c1 Show InChI InChI=1S/C17H15Cl2N3O4/c1-20-15(23)9-3-6-14(26-2)13(7-9)21-17(25)22-16(24)11-5-4-10(18)8-12(11)19/h3-8H,1-2H3,(H,20,23)(H2,21,22,24,25)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	302	n/a	n/a	n/a	n/a	7.2	n/a
Sanofi-Aventis Deutschland GmbH Curated by ChEMBL					Assay Description Logarithmic inhibitory concentration against human liver glycogen phosphorylase enzyme by the addition of glucose-1-phosphate and incubated for 40 mi...				J Med Chem 48: 6178-93 (2005) Article DOI: 10.1021/jm049034y BindingDB Entry DOI: 10.7270/Q2FT8KJ5
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Homo sapiens (Human))	BDBM50174365 (4-[3-(2,4-Dichloro-benzoyl)-ureido]-3-methoxy-N-me...) Show SMILES CNC(=O)c1ccc(NC(=O)NC(=O)c2ccc(Cl)cc2Cl)c(OC)c1 Show InChI InChI=1S/C17H15Cl2N3O4/c1-20-15(23)9-3-6-13(14(7-9)26-2)21-17(25)22-16(24)11-5-4-10(18)8-12(11)19/h3-8H,1-2H3,(H,20,23)(H2,21,22,24,25)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	407	n/a	n/a	n/a	n/a	7.2	n/a
Sanofi-Aventis Deutschland GmbH Curated by ChEMBL					Assay Description Logarithmic inhibitory concentration against human liver glycogen phosphorylase enzyme by the addition of glucose-1-phosphate and incubated for 40 mi...				J Med Chem 48: 6178-93 (2005) Article DOI: 10.1021/jm049034y BindingDB Entry DOI: 10.7270/Q2FT8KJ5
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Homo sapiens (Human))	BDBM50174365 (4-[3-(2,4-Dichloro-benzoyl)-ureido]-3-methoxy-N-me...) Show SMILES CNC(=O)c1ccc(NC(=O)NC(=O)c2ccc(Cl)cc2Cl)c(OC)c1 Show InChI InChI=1S/C17H15Cl2N3O4/c1-20-15(23)9-3-6-13(14(7-9)26-2)21-17(25)22-16(24)11-5-4-10(18)8-12(11)19/h3-8H,1-2H3,(H,20,23)(H2,21,22,24,25)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	410	n/a	n/a	n/a	n/a	7.2	n/a
Sanofi-Aventis Deutschland GmbH Curated by ChEMBL					Assay Description Inhibitory concentration against human liver glycogen phosphorylase enzyme by the addition of glucose-1-phosphate upon incubating for 40 min at 25 de...				J Med Chem 48: 6178-93 (2005) Article DOI: 10.1021/jm049034y BindingDB Entry DOI: 10.7270/Q2FT8KJ5
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Homo sapiens (Human))	BDBM50174391 (3-Chloro-4-[3-(2,4-dichloro-benzoyl)-ureido]-benzo...) Show SMILES OC(=O)c1ccc(NC(=O)NC(=O)c2ccc(Cl)cc2Cl)c(Cl)c1 Show InChI InChI=1S/C15H9Cl3N2O4/c16-8-2-3-9(10(17)6-8)13(21)20-15(24)19-12-4-1-7(14(22)23)5-11(12)18/h1-6H,(H,22,23)(H2,19,20,21,24)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	417	n/a	n/a	n/a	n/a	7.2	n/a
Sanofi-Aventis Deutschland GmbH Curated by ChEMBL					Assay Description Logarithmic inhibitory concentration against human liver glycogen phosphorylase enzyme by the addition of glucose-1-phosphate and incubated for 40 mi...				J Med Chem 48: 6178-93 (2005) Article DOI: 10.1021/jm049034y BindingDB Entry DOI: 10.7270/Q2FT8KJ5
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Homo sapiens (Human))	BDBM50174391 (3-Chloro-4-[3-(2,4-dichloro-benzoyl)-ureido]-benzo...) Show SMILES OC(=O)c1ccc(NC(=O)NC(=O)c2ccc(Cl)cc2Cl)c(Cl)c1 Show InChI InChI=1S/C15H9Cl3N2O4/c16-8-2-3-9(10(17)6-8)13(21)20-15(24)19-12-4-1-7(14(22)23)5-11(12)18/h1-6H,(H,22,23)(H2,19,20,21,24)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	420	n/a	n/a	n/a	n/a	7.2	n/a
Sanofi-Aventis Deutschland GmbH Curated by ChEMBL					Assay Description Inhibitory concentration against human liver glycogen phosphorylase enzyme by the addition of glucose-1-phosphate upon incubating for 40 min at 25 de...				J Med Chem 48: 6178-93 (2005) Article DOI: 10.1021/jm049034y BindingDB Entry DOI: 10.7270/Q2FT8KJ5
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Homo sapiens (Human))	BDBM50174396 (4-[3-(2-Chloro-4,5-difluoro-benzoyl)-ureido]-3-(2,...) Show SMILES OC(=O)c1ccc(NC(=O)NC(=O)c2cc(F)c(F)cc2Cl)c(OCC(F)(F)F)c1 Show InChI InChI=1S/C17H10ClF5N2O5/c18-9-5-11(20)10(19)4-8(9)14(26)25-16(29)24-12-2-1-7(15(27)28)3-13(12)30-6-17(21,22)23/h1-5H,6H2,(H,27,28)(H2,24,25,26,29)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	447	n/a	n/a	n/a	n/a	7.2	n/a
Sanofi-Aventis Deutschland GmbH Curated by ChEMBL					Assay Description Logarithmic inhibitory concentration against human liver glycogen phosphorylase enzyme by the addition of glucose-1-phosphate and incubated for 40 mi...				J Med Chem 48: 6178-93 (2005) Article DOI: 10.1021/jm049034y BindingDB Entry DOI: 10.7270/Q2FT8KJ5
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Homo sapiens (Human))	BDBM50174396 (4-[3-(2-Chloro-4,5-difluoro-benzoyl)-ureido]-3-(2,...) Show SMILES OC(=O)c1ccc(NC(=O)NC(=O)c2cc(F)c(F)cc2Cl)c(OCC(F)(F)F)c1 Show InChI InChI=1S/C17H10ClF5N2O5/c18-9-5-11(20)10(19)4-8(9)14(26)25-16(29)24-12-2-1-7(15(27)28)3-13(12)30-6-17(21,22)23/h1-5H,6H2,(H,27,28)(H2,24,25,26,29)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	450	n/a	n/a	n/a	n/a	7.2	n/a
Sanofi-Aventis Deutschland GmbH Curated by ChEMBL					Assay Description Inhibitory concentration against human liver glycogen phosphorylase enzyme by the addition of glucose-1-phosphate upon incubating for 40 min at 25 de...				J Med Chem 48: 6178-93 (2005) Article DOI: 10.1021/jm049034y BindingDB Entry DOI: 10.7270/Q2FT8KJ5
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Homo sapiens (Human))	BDBM50174398 (4-[3-(2,4-Dichloro-benzoyl)-ureido]-3-methoxy-benz...) Show SMILES COc1cc(ccc1NC(=O)NC(=O)c1ccc(Cl)cc1Cl)C(O)=O Show InChI InChI=1S/C16H12Cl2N2O5/c1-25-13-6-8(15(22)23)2-5-12(13)19-16(24)20-14(21)10-4-3-9(17)7-11(10)18/h2-7H,1H3,(H,22,23)(H2,19,20,21,24)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	510	n/a	n/a	n/a	n/a	7.2	n/a
Sanofi-Aventis Deutschland GmbH Curated by ChEMBL					Assay Description Inhibitory concentration against human liver glycogen phosphorylase enzyme by the addition of glucose-1-phosphate upon incubating for 40 min at 25 de...				J Med Chem 48: 6178-93 (2005) Article DOI: 10.1021/jm049034y BindingDB Entry DOI: 10.7270/Q2FT8KJ5
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Homo sapiens (Human))	BDBM50174404 (4-[3-(2-Chloro-4-fluoro-benzoyl)-ureido]-2-hydroxy...) Show SMILES OC(=O)c1ccc(NC(=O)NC(=O)c2ccc(F)cc2Cl)cc1O Show InChI InChI=1S/C15H10ClFN2O5/c16-11-5-7(17)1-3-9(11)13(21)19-15(24)18-8-2-4-10(14(22)23)12(20)6-8/h1-6,20H,(H,22,23)(H2,18,19,21,24)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	510	n/a	n/a	n/a	n/a	7.2	n/a
Sanofi-Aventis Deutschland GmbH Curated by ChEMBL					Assay Description Inhibitory concentration against human liver glycogen phosphorylase enzyme by the addition of glucose-1-phosphate upon incubating for 40 min at 25 de...				J Med Chem 48: 6178-93 (2005) Article DOI: 10.1021/jm049034y BindingDB Entry DOI: 10.7270/Q2FT8KJ5
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Homo sapiens (Human))	BDBM50174404 (4-[3-(2-Chloro-4-fluoro-benzoyl)-ureido]-2-hydroxy...) Show SMILES OC(=O)c1ccc(NC(=O)NC(=O)c2ccc(F)cc2Cl)cc1O Show InChI InChI=1S/C15H10ClFN2O5/c16-11-5-7(17)1-3-9(11)13(21)19-15(24)18-8-2-4-10(14(22)23)12(20)6-8/h1-6,20H,(H,22,23)(H2,18,19,21,24)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	513	n/a	n/a	n/a	n/a	7.2	n/a
Sanofi-Aventis Deutschland GmbH Curated by ChEMBL					Assay Description Logarithmic inhibitory concentration against human liver glycogen phosphorylase enzyme by the addition of glucose-1-phosphate and incubated for 40 mi...				J Med Chem 48: 6178-93 (2005) Article DOI: 10.1021/jm049034y BindingDB Entry DOI: 10.7270/Q2FT8KJ5
					More data for this Ligand-Target Pair
Glycogen phosphorylase, liver form (Homo sapiens (Human))	BDBM50174398 (4-[3-(2,4-Dichloro-benzoyl)-ureido]-3-methoxy-benz...) Show SMILES COc1cc(ccc1NC(=O)NC(=O)c1ccc(Cl)cc1Cl)C(O)=O Show InChI InChI=1S/C16H12Cl2N2O5/c1-25-13-6-8(15(22)23)2-5-12(13)19-16(24)20-14(21)10-4-3-9(17)7-11(10)18/h2-7H,1H3,(H,22,23)(H2,19,20,21,24)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	513	n/a	n/a	n/a	n/a	7.2	n/a
Sanofi-Aventis Deutschland GmbH Curated by ChEMBL					Assay Description Logarithmic inhibitory concentration against human liver glycogen phosphorylase enzyme by the addition of glucose-1-phosphate and incubated for 40 mi...				J Med Chem 48: 6178-93 (2005) Article DOI: 10.1021/jm049034y BindingDB Entry DOI: 10.7270/Q2FT8KJ5
					More data for this Ligand-Target Pair

Displayed 1 to 50 (of 85 total )  |  Next  |  Last  >>

Jump to: