Compile Data Set for Download or QSAR

Found 5 hits of ki for monomerid = 50057719   

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, brain form (Homo sapiens (Human))	BDBM50057719 (3,4,5-Trihydroxy-6-hydroxymethyl-tetrahydro-pyran-...) Show SMILES [H][C@]1(O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)C(=O)NN Show InChI InChI=1S/C7H14N2O6/c8-9-7(14)6-5(13)4(12)3(11)2(1-10)15-6/h2-6,10-13H,1,8H2,(H,9,14)/t2-,3-,4+,5-,6-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	3.98E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Philipps-Universit£t Marburg Curated by ChEMBL					Assay Description Inhibitory activity against Pig Skeletal Glycogen Phosphorylase b				J Med Chem 45: 4153-70 (2002) Article DOI: 10.1021/jm020808p BindingDB Entry DOI: 10.7270/Q2KH0R3H
					More data for this Ligand-Target Pair
Glycogen phosphorylase, brain form (Homo sapiens (Human))	BDBM50057719 (3,4,5-Trihydroxy-6-hydroxymethyl-tetrahydro-pyran-...) Show SMILES [H][C@]1(O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)C(=O)NN Show InChI InChI=1S/C7H14N2O6/c8-9-7(14)6-5(13)4(12)3(11)2(1-10)15-6/h2-6,10-13H,1,8H2,(H,9,14)/t2-,3-,4+,5-,6-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	4.00E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Perugia Curated by ChEMBL					Assay Description Inhibition of rabbit glycogen phosphorylase B enzyme				J Med Chem 40: 1455-64 (1997) Article DOI: 10.1021/jm9608016 BindingDB Entry DOI: 10.7270/Q26T0N9N
					More data for this Ligand-Target Pair
Glycogen phosphorylase, brain form (Homo sapiens (Human))	BDBM50057719 (3,4,5-Trihydroxy-6-hydroxymethyl-tetrahydro-pyran-...) Show SMILES [H][C@]1(O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)C(=O)NN Show InChI InChI=1S/C7H14N2O6/c8-9-7(14)6-5(13)4(12)3(11)2(1-10)15-6/h2-6,10-13H,1,8H2,(H,9,14)/t2-,3-,4+,5-,6-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	4.00E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Perugia Curated by ChEMBL					Assay Description Inhibition of rabbit glycogen phosphorylase B enzyme				J Med Chem 40: 1455-64 (1997) Article DOI: 10.1021/jm9608016 BindingDB Entry DOI: 10.7270/Q26T0N9N
					More data for this Ligand-Target Pair
Glycogen phosphorylase, muscle form (Homo sapiens (Human))	BDBM50057719 (3,4,5-Trihydroxy-6-hydroxymethyl-tetrahydro-pyran-...) Show SMILES [H][C@]1(O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)C(=O)NN Show InChI InChI=1S/C7H14N2O6/c8-9-7(14)6-5(13)4(12)3(11)2(1-10)15-6/h2-6,10-13H,1,8H2,(H,9,14)/t2-,3-,4+,5-,6-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	2.52E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Alcala Curated by ChEMBL					Assay Description Inhibitory activity against rabbit muscle glycogen phosphorylase				J Med Chem 40: 4089-102 (1998) Checked by Author Article DOI: 10.1021/jm970273d BindingDB Entry DOI: 10.7270/Q2S46TGM
					More data for this Ligand-Target Pair
Glycogen phosphorylase, muscle form (Homo sapiens (Human))	BDBM50057719 (3,4,5-Trihydroxy-6-hydroxymethyl-tetrahydro-pyran-...) Show SMILES [H][C@]1(O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)C(=O)NN Show InChI InChI=1S/C7H14N2O6/c8-9-7(14)6-5(13)4(12)3(11)2(1-10)15-6/h2-6,10-13H,1,8H2,(H,9,14)/t2-,3-,4+,5-,6-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	2.52E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Alcala Curated by ChEMBL					Assay Description Inhibitory activity against rabbit muscle glycogen phosphorylase				J Med Chem 40: 4089-102 (1998) Checked by Author Article DOI: 10.1021/jm970273d BindingDB Entry DOI: 10.7270/Q2S46TGM
					More data for this Ligand-Target Pair