DRUG-PATHWAY

DRUGs and PATHWAYs

PATHWAY_NAME	REACTOME_ID	KEGG_ID	DRUG_NAME	PUBCHEM_CID	Datasource
Hawkinsinuria	0	0	Methylammonium	9548602	smpdb
Disulfiram Action Pathway	R-ALL-9693326	0	Methylammonium	9548602	smpdb
Dopamine beta-Hydroxylase Deficiency	R-HSA-390651	0	Methylammonium	9548602	smpdb
Tyrosine Metabolism	R-HSA-8963691	map00350	Methylammonium	9548602	smpdb
Citalopram Action Pathway	R-ALL-9714383	0	Methylammonium	9548602	smpdb
Pyruvate Decarboxylase E1 Component Deficiency	R-HSA-204168	0	Propylene glycol	443955	smpdb
Pyruvate Kinase Deficiency	R-HSA-450668	0	Propylene glycol	443955	smpdb
Primary Hyperoxaluria II, PH2	R-HSA-5601905	0	Propylene glycol	443955	smpdb
Pyruvate Dehydrogenase Complex Deficiency	R-HSA-204174	0	Propylene glycol	443955	smpdb
Pyruvate Metabolism	R-HSA-70268	map00620	Propylene glycol	443955	smpdb
Leigh Syndrome	R-HSA-2206302	0	Propylene glycol	443955	smpdb
Pyrimidine Metabolism	R-HSA-500753	map00240	Dihydrouracil	439216	smpdb
beta-Ureidopropionase Deficiency	R-HSA-5602680	0	Dihydrouracil	439216	smpdb
GABA-Transaminase Deficiency	R-HSA-5602680	0	Dihydrouracil	439216	smpdb
beta-Alanine Metabolism	R-ALL-352021	map00410	Dihydrouracil	439216	smpdb
Carnosinuria, Carnosinemia	0	0	Dihydrouracil	439216	smpdb
UMP Synthase Deficiency	R-ALL-418075	0	Dihydrouracil	439216	smpdb
Dihydropyrimidinase Deficiency	R-HSA-5602680	0	Dihydrouracil	439216	smpdb
MNGIE	0	0	Dihydrouracil	439216	smpdb
Congenital Disorder of Glycosylation CDG-IId	R-HSA-5619078	0	Uridine diphosphate glucose	439302	smpdb