null

SMILES: OCC1O[C@]2(NC(=O)NC2=O)C(O)[C@@H](O)[C@@H]1O

InChI Key: InChIKey=QRXBDPYWCAAAAI-QNDJJFHGSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50102884   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kcal/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Glycogen phosphorylase, brain form (Homo sapiens (Human))	BDBM50102884 (8,9,10-Trihydroxy-7-hydroxymethyl-6-oxa-1,3-diaza-...) Show SMILES OCC1O[C@]2(NC(=O)NC2=O)C(O)[C@@H](O)[C@@H]1O Show InChI InChI=1S/C8H12N2O7/c11-1-2-3(12)4(13)5(14)8(17-2)6(15)9-7(16)10-8/h2-5,11-14H,1H2,(H2,9,10,15,16)/t2?,3-,4+,5?,8-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	1.05E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Debrecen Curated by ChEMBL					Assay Description Inhibitory activity against muscle Glycogen Phosphorylase b				J Med Chem 44: 2843-8 (2001) BindingDB Entry DOI: 10.7270/Q2NV9JZQ
					More data for this Ligand-Target Pair
Glycogen phosphorylase, brain form (Homo sapiens (Human))	BDBM50102884 (8,9,10-Trihydroxy-7-hydroxymethyl-6-oxa-1,3-diaza-...) Show SMILES OCC1O[C@]2(NC(=O)NC2=O)C(O)[C@@H](O)[C@@H]1O Show InChI InChI=1S/C8H12N2O7/c11-1-2-3(12)4(13)5(14)8(17-2)6(15)9-7(16)10-8/h2-5,11-14H,1H2,(H2,9,10,15,16)/t2?,3-,4+,5?,8-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	3.20E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Debrecen Curated by ChEMBL					Assay Description Inhibitory activity against muscle Glycogen Phosphorylase b				J Med Chem 44: 2843-8 (2001) BindingDB Entry DOI: 10.7270/Q2NV9JZQ
					More data for this Ligand-Target Pair