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Drug-Pathway
DRUGs and PATHWAYs
PATHWAY_NAME REACTOME_ID KEGG_ID DRUG_NAME PUBCHEM_CID Datasource
Creatine Deficiency, Guanidinoacetate Methyltransferase Deficiency 0 0 Heme 446156 smpdb
Adrenal Hyperplasia Type 3 or Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency 0 0 Heme 446156 smpdb
Congenital Bile Acid Synthesis Defect Type III R-HSA-194068 0 Heme 446156 smpdb
Apparent Mineralocorticoid Excess Syndrome R-HSA-193993 0 Heme 446156 smpdb
Congenital Erythropoietic Porphyria or Gunther Disease 0 0 Heme 446156 smpdb
Rosiglitazone Metabolism Pathway R-ALL-9732641 0 Heme 446156 smpdb
CHILD Syndrome R-HSA-2206302 0 Heme 446156 smpdb
Artemether Metabolism Pathway R-HSA-1430728 0 Heme 446156 smpdb
Nicotine Action Pathway R-ALL-30661 0 Heme 446156 smpdb
Lovastatin Action Pathway R-ALL-9705577 0 Heme 446156 smpdb
Ifosfamide Action Pathway R-ALL-9713784 0 Heme 446156 smpdb
Fluvastatin Action Pathway R-ALL-9705591 0 Heme 446156 smpdb
Congenital Lipoid Adrenal Hyperplasia or Lipoid CAH 0 0 Heme 446156 smpdb
Acetaminophen Metabolism Pathway R-ALL-39427 0 Heme 446156 smpdb
Smith-Lemli-Opitz Syndrome R-HSA-2206302 0 Heme 446156 smpdb
Thioguanine Action Pathway R-ALL-9679095 0 Heme 446156 smpdb
Cholesteryl Ester Storage Disease R-HSA-1643685 0 Heme 446156 smpdb
Clopidogrel Action Pathway R-ALL-9611274 0 Heme 446156 smpdb
Chondrodysplasia Punctata II, X-Linked Dominant 0 0 Heme 446156 smpdb
Xanthine Dehydrogenase Deficiency R-HSA-9027561 0 Heme 446156 smpdb