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Drug-Pathway
DRUGs and PATHWAYs
PATHWAY_NAME REACTOME_ID KEGG_ID DRUG_NAME PUBCHEM_CID Datasource
Retinol Metabolism R-HSA-1430728 map00830 Oxygen 4831 pubchem
Acute Intermittent Porphyria Q9NX94 0 Oxygen 4831 pubchem
Porphyria Variegata #N/A #N/A Oxygen 4831 pubchem
Congenital Erythropoietic Porphyria or Gunther Disease 0 0 Oxygen 4831 pubchem
Adrenal Hyperplasia Type 3 or Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency 0 0 Oxygen 4831 pubchem
Congenital Lipoid Adrenal Hyperplasia or Lipoid CAH 0 0 Oxygen 4831 pubchem
Adrenal Hyperplasia Type 5 or Congenital Adrenal Hyperplasia Due to 17 alpha-Hydroxylase Deficiency 0 0 Oxygen 4831 pubchem
Alkaptonuria R-HSA-71164 0 Oxygen 4831 pubchem
Hawkinsinuria 0 0 Oxygen 4831 pubchem
Tyrosinemia Type I R-ALL-9605649 0 Oxygen 4831 pubchem
Congenital Bile Acid Synthesis Defect Type II R-HSA-194068 0 Oxygen 4831 pubchem
Congenital Bile Acid Synthesis Defect Type III R-HSA-194068 0 Oxygen 4831 pubchem
Familial Hypercholanemia #N/A #N/A Oxygen 4831 pubchem
Zellweger Syndrome R-HSA-2206302 0 Oxygen 4831 pubchem
Cerebrotendinous Xanthomatosis #N/A #N/A Oxygen 4831 pubchem
Dimethylglycine Dehydrogenase Deficiency R-HSA-9027561 0 Oxygen 4831 pubchem
Dihydropyrimidine Dehydrogenase Deficiency #N/A #N/A Oxygen 4831 pubchem
Sarcosinemia R-HSA-6797913 0 Oxygen 4831 pubchem
Non-Ketotic Hyperglycinemia R-HSA-6783984 0 Oxygen 4831 pubchem
Vitamin A Deficiency R-HSA-8877627 0 Oxygen 4831 pubchem