DRUG-PATHWAY

DRUGs and PATHWAYs

PATHWAY_NAME	REACTOME_ID	KEGG_ID	DRUG_NAME	PUBCHEM_CID	Datasource
Mucopolysaccharidosis VII. Sly Syndrome	R-HSA-2206292	0	NADH	121396	smpdb
Hyperprolinemia Type I	R-ALL-9605649	0	NADH	121396	smpdb
Congenital Bile Acid Synthesis Defect Type III	R-HSA-194068	0	NADH	121396	smpdb
3-Hydroxyisobutyric Acid Dehydrogenase Deficiency	R-HSA-9027561	0	NADH	121396	smpdb
Dihydropyrimidine Dehydrogenase Deficiency	R-HSA-9027561	0	NADH	121396	smpdb
The Oncogenic Action of D-2-Hydroxyglutarate in Hydroxygluaricaciduria	#N/A	#N/A	NADH	121396	smpdb
De Novo Triacylglycerol Biosynthesis	R-HSA-1660661	0	NADH	121396	smpdb
Citalopram Action Pathway	R-ALL-9714383	0	NADH	121396	smpdb
Methylenetetrahydrofolate Reductase Deficiency	R-HSA-9024779	0	Folic acid	107689	smpdb
Methotrexate Action Pathway	R-ALL-9660245	0	Folic acid	107689	smpdb
Folate Malabsorption, Hereditary	R-HSA-5657560	0	Folic acid	107689	smpdb
Folate Metabolism	R-HSA-196757	0	Folic acid	107689	smpdb
Alpha Linolenic Acid and Linoleic Acid Metabolism	R-HSA-2046105	0	Eicosapentaenoic acid	445580	smpdb
Selenoamino Acid Metabolism	R-HSA-2408522	0	L-Alanine	107807	smpdb
Neomycin Action Pathway	R-HSA-9639775	0	L-Alanine	107807	smpdb
Hyperinsulinism-Hyperammonemia Syndrome	R-HSA-2206302	0	L-Alanine	107807	smpdb
Troleandomycin Action Pathway	R-ALL-9679059	0	L-Alanine	107807	smpdb
Ornithine Transcarbamylase Deficiency	R-HSA-5602680	0	L-Alanine	107807	smpdb
Sarcosinemia	R-HSA-6797913	0	L-Alanine	107807	smpdb
Paromomycin Action Pathway	R-HSA-9639775	0	L-Alanine	107807	smpdb