{"chebi_id":"58052","chebi_name":"UDP-\u03b1-D-glucuronate(3\u2212)","chebi_synonyms":["UDP-\u03b1-D-glucuronate","UDP-\u03b1-D-glucuronate trianion"],"diffprof_id_observed":["MTBLS87_0004_00000001","MTBLS88_0003_00000001"],"diffprof_id_var_observed":["MTBLS87_0004_00000001","MTBLS88_0003_00000001"],"inchikey":"HDYANYHVCAPMJV-LXQIFKJMSA-K","inn_name":"","iupac_name":"","num_study_observed":2,"reactome_ids":["R-HSA-1430728","R-HSA-156580","R-HSA-156588","R-HSA-1630316","R-HSA-1638091","R-HSA-1643685","R-HSA-173599","R-HSA-1793185","R-HSA-189445","R-HSA-189483","R-HSA-1971475","R-HSA-2022870","R-HSA-2022928","R-HSA-211859","R-HSA-2142845","R-HSA-2161522","R-HSA-2161541","R-HSA-3560782","R-HSA-3560801","R-HSA-3595177","R-HSA-3656237","R-HSA-3656253","R-HSA-3781865","R-HSA-382551","R-HSA-392499","R-HSA-425397","R-HSA-425407","R-HSA-5173105","R-HSA-5579002","R-HSA-5579016","R-HSA-5579020","R-HSA-5579029","R-HSA-5668914","R-HSA-597592","R-HSA-71387","R-HSA-727802","R-HSA-8931838","R-HSA-9748784","R-HSA-9749641","R-HSA-9753281","R-HSA-9754706","R-HSA-9757110","R-HSA-9939291"],"reactome_names":["Metabolism","Phase II - Conjugation of compounds","Glucuronidation","Glycosaminoglycan metabolism","Heparan sulfate/heparin (HS-GAG) metabolism","Disease","Formation of the active cofactor, UDP-glucuronate","Chondroitin sulfate/dermatan sulfate metabolism","Metabolism of porphyrins","Heme degradation","Glycosaminoglycan-protein linkage region biosynthesis","CS-GAG biosynthesis","HS-GAG biosynthesis","Biological oxidations","Hyaluronan metabolism","Abacavir ADME","Abacavir metabolism","Diseases associated with glycosaminoglycan metabolism","Defective B3GAT3 causes JDSSDHD","Defective CHSY1 causes TPBS","Defective EXT2 causes exostoses 2","Defective EXT1 causes exostoses 1, TRPS2 and CHDS","Diseases of glycosylation","Transport of small molecules","Metabolism of proteins","Transport of vitamins, nucleosides, and related molecules","SLC-mediated transmembrane transport","O-linked glycosylation","Defective UGT1A1 causes hyperbilirubinemia","Defective UGT1A4 causes hyperbilirubinemia","Defective SLC35D1 causes SCHBCKD","Metabolic disorders of biological oxidation enzymes","Diseases of metabolism","Post-translational protein modification","Metabolism of carbohydrates and carbohydrate derivatives","Transport of nucleotide sugars","DAG1 glycosylations","Drug ADME","Aspirin ADME","Paracetamol ADME","Atorvastatin ADME","Prednisone ADME","Matriglycan biosynthesis on DAG1"],"study_id_observed":["MTBLS87","MTBLS88"],"study_id_var_observed":["MTBLS87","MTBLS88"],"synonym_name":"UDP-\u03b1-<small>D</small>-glucuronate trianion"}