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Drug-Pathway
DRUGs and PATHWAYs
PATHWAY_NAME REACTOME_ID KEGG_ID DRUG_NAME PUBCHEM_CID Datasource
Glycogen Storage Disease Type 1A or Von Gierke Disease 0 0 Phosphoenolpyruvic acid 5280363 smpdb
Glycogenosis, Type IB R-HSA-8848137 0 Phosphoenolpyruvic acid 5280363 smpdb
Fanconi-Bickel Syndrome R-HSA-5619098 0 Phosphoenolpyruvic acid 5280363 smpdb
Glycogenosis, Type IC R-ALL-9605649 0 Phosphoenolpyruvic acid 5280363 smpdb
Vitamin K Metabolism R-HSA-6806664 0 Oxidized dithiothreitol 11318905 smpdb
Citalopram Metabolism Pathway R-ALL-9714383 0 Methylamine 439199 smpdb
Alkaptonuria R-HSA-71164 0 Methylamine 439199 smpdb
Tyrosinemia, Transient, of the Newborn R-HSA-5683209 0 Methylamine 439199 smpdb
Monoamine Oxidase-A Deficiency R-HSA-5602680 0 Methylamine 439199 smpdb
Tyrosinemia Type I R-ALL-9605649 0 Methylamine 439199 smpdb
Hawkinsinuria 0 0 Methylamine 439199 smpdb
Disulfiram Action Pathway R-ALL-9693326 0 Methylamine 439199 smpdb
Dopamine beta-Hydroxylase Deficiency R-HSA-390651 0 Methylamine 439199 smpdb
Tyrosine Metabolism R-HSA-8963691 map00350 Methylamine 439199 smpdb
Citalopram Action Pathway R-ALL-9714383 0 Methylamine 439199 smpdb
Citalopram Metabolism Pathway R-ALL-9714383 0 Methylammonium 9548602 smpdb
Alkaptonuria R-HSA-71164 0 Methylammonium 9548602 smpdb
Tyrosinemia, Transient, of the Newborn R-HSA-5683209 0 Methylammonium 9548602 smpdb
Monoamine Oxidase-A Deficiency R-HSA-5602680 0 Methylammonium 9548602 smpdb
Tyrosinemia Type I R-ALL-9605649 0 Methylammonium 9548602 smpdb