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KEGG DRUG

Search results

No.

KEGG DRUG

DrugBank

Drug (Description in trials)

KEGG GENES

KEGG PATHWAY

Disease ID

Arginine 💬

[1] Arginine

[16] 2, 21, 46, 57, 58, 67, 72, 96, 97, 98, 113, 210, 223, 225, 251, 299 💬

Disease ID	Name
2	Amyotrophic lateral sclerosis
21	Mitochondrial disease
46	Malignant rheumatoid arthritis
57	Idiopathic dilated cardiomyopathy
58	Hypertrophic cardiomyopathy
67	Polycystic kidney disease
72	Pituitary ADH secretion disorder
96	Crohn disease
97	Ulcerative colitis
98	Eosinophilic gastro-intestinal disorder
113	Muscular dystrophy
210	Single Ventricle
223	Primary membranoproliferative glomerulonephritis
225	Congenital nephrogenic diabetes insipidus
251	Urea cycle disorder
299	Cystic fibrosis

Arginine hydrochloride 💬

[1] Arginine

[16] 2, 21, 46, 57, 58, 67, 72, 96, 97, 98, 113, 210, 223, 225, 251, 299 💬

Disease ID	Name
2	Amyotrophic lateral sclerosis
21	Mitochondrial disease
46	Malignant rheumatoid arthritis
57	Idiopathic dilated cardiomyopathy
58	Hypertrophic cardiomyopathy
67	Polycystic kidney disease
72	Pituitary ADH secretion disorder
96	Crohn disease
97	Ulcerative colitis
98	Eosinophilic gastro-intestinal disorder
113	Muscular dystrophy
210	Single Ventricle
223	Primary membranoproliferative glomerulonephritis
225	Congenital nephrogenic diabetes insipidus
251	Urea cycle disorder
299	Cystic fibrosis

Arginine hydrochloride 💬

[1] Arginine

[16] 2, 21, 46, 57, 58, 67, 72, 96, 97, 98, 113, 210, 223, 225, 251, 299 💬

Disease ID	Name
2	Amyotrophic lateral sclerosis
21	Mitochondrial disease
46	Malignant rheumatoid arthritis
57	Idiopathic dilated cardiomyopathy
58	Hypertrophic cardiomyopathy
67	Polycystic kidney disease
72	Pituitary ADH secretion disorder
96	Crohn disease
97	Ulcerative colitis
98	Eosinophilic gastro-intestinal disorder
113	Muscular dystrophy
210	Single Ventricle
223	Primary membranoproliferative glomerulonephritis
225	Congenital nephrogenic diabetes insipidus
251	Urea cycle disorder
299	Cystic fibrosis

Desmopressin 💬

[1] Desmopressin

[2] Desmopressin; Desmopressin acetate

[2] AVPR2,
F8 💬

[5] Complement and coagulation cascades, Hormone signaling, Neuroactive ligand-receptor interaction, Phospholipase D signaling pathway, Vasopressin-regulated water reabsorption 💬

[8] 6, 22, 64, 72, 75, 223, 225, 288 💬

Disease ID	Name
6	Parkinson disease
22	Moyamoya disease
64	Thrombotic thrombocytopenic purpura
72	Pituitary ADH secretion disorder
75	Cushing disease
223	Primary membranoproliferative glomerulonephritis
225	Congenital nephrogenic diabetes insipidus
288	Autoimmune acquired coagulation factor deficiency

Desmopressin acetate

💬

[1] Desmopressin

[2] Desmopressin; Desmopressin acetate

[2] AVPR2,
F8 💬

[5] Complement and coagulation cascades, Hormone signaling, Neuroactive ligand-receptor interaction, Phospholipase D signaling pathway, Vasopressin-regulated water reabsorption 💬

[8] 6, 22, 64, 72, 75, 223, 225, 288 💬

Disease ID	Name
6	Parkinson disease
22	Moyamoya disease
64	Thrombotic thrombocytopenic purpura
72	Pituitary ADH secretion disorder
75	Cushing disease
223	Primary membranoproliferative glomerulonephritis
225	Congenital nephrogenic diabetes insipidus
288	Autoimmune acquired coagulation factor deficiency

Empagliflozin 💬

[1] Empagliflozin

[17] 28, 46, 57, 58, 65, 67, 72, 77, 86, 96, 97, 113, 222, 223, 257, 298, 299 💬

Disease ID	Name
28	Systemic amyloidosis
46	Malignant rheumatoid arthritis
57	Idiopathic dilated cardiomyopathy
58	Hypertrophic cardiomyopathy
65	Primary immunodeficiency
67	Polycystic kidney disease
72	Pituitary ADH secretion disorder
77	Growth hormone secreting pituitary adenoma
86	Pulmonary arterial hypertension
96	Crohn disease
97	Ulcerative colitis
113	Muscular dystrophy
222	Primary nephrotic syndrome
223	Primary membranoproliferative glomerulonephritis
257	Hepatic glycogenosis
298	Hereditary pancreatitis
299	Cystic fibrosis

Exenatide 💬

[1] Exenatide

[1] GLP1R 💬

[4] Hormone signaling, Insulin secretion, Neuroactive ligand-receptor interaction, cAMP signaling pathway 💬

[6] 6, 17, 72, 78, 193, 233 💬

Melatonin 💬

[1] Melatonin

[2] MTNR1A,
MTNR1B 💬

[2] Circadian entrainment, Neuroactive ligand-receptor interaction 💬

[18] 2, 6, 8, 13, 37, 46, 49, 72, 78, 86, 90, 96, 97, 145, 149, 159, 202, 265 💬

Disease ID	Name
2	Amyotrophic lateral sclerosis
6	Parkinson disease
8	Huntington disease
13	Multiple sclerosis/Neuromyelitis optica
37	Generalised pustular psoriasis
46	Malignant rheumatoid arthritis
49	Systemic lupus erythematosus
72	Pituitary ADH secretion disorder
78	Hypopituitarism
86	Pulmonary arterial hypertension
90	Retinitis pigmentosa
96	Crohn disease
97	Ulcerative colitis
145	West syndrome
149	Hemiconvulsion hemiplegia epilepsy syndrome
159	Xeroderma pigmentosum
202	Smith-Magenis syndrome
265	Lipodystrophy

Oxytocin 💬

[1] Oxytocin

[1] OXTR 💬

[5] Calcium signaling pathway, Hormone signaling, Neuroactive ligand-receptor interaction, Oxytocin signaling pathway, cAMP signaling pathway 💬

[8] 6, 70, 72, 127, 168, 193, 206, 226 💬

Disease ID	Name
6	Parkinson disease
70	Spinal stenosis
72	Pituitary ADH secretion disorder
127	Frontotemporal lobar degeneration
168	Ehlers-Danlos syndrome
193	Prader-Willi syndrome
206	Fragile X syndrome
226	Interstitial cystitis with Hunners ulcer

Tolvaptan 💬

[1] Tolvaptan

[1] AVPR2 💬

[4] Hormone signaling, Neuroactive ligand-receptor interaction, Phospholipase D signaling pathway, Vasopressin-regulated water reabsorption 💬

[5] 67, 72, 86, 222, 225 💬

Urea 💬

[1] Urea

[2] 72, 251 💬

Urea C13 💬

[1] Urea

[2] 72, 251 💬

Water

💬

[1] Water

[36] 2, 3, 5, 6, 13, 17, 19, 22, 35, 46, 49, 51, 53, 56, 57, 62, 63, 64, 65, 66, 67, 70, 72, 85, 86, 96, 97, 206, 215, 225, 226, 230, 240, 274, 278, 299 💬

Disease ID	Name
2	Amyotrophic lateral sclerosis
3	Spinal muscular atrophy
5	Progressive supranuclear palsy
6	Parkinson disease
13	Multiple sclerosis/Neuromyelitis optica
17	Multiple system atrophy
19	Lysosomal storage disease
22	Moyamoya disease
35	Pemphigus
46	Malignant rheumatoid arthritis
49	Systemic lupus erythematosus
51	Scleroderma
53	Sjogren syndrome
56	Behcet disease
57	Idiopathic dilated cardiomyopathy
62	Paroxysmal nocturnal hemoglobinuria
63	Idiopathic thrombocytopenic purpura
64	Thrombotic thrombocytopenic purpura
65	Primary immunodeficiency
66	IgA nephropathy
67	Polycystic kidney disease
70	Spinal stenosis
72	Pituitary ADH secretion disorder
85	Idiopathic interstitial pneumonia
86	Pulmonary arterial hypertension
96	Crohn disease
97	Ulcerative colitis
206	Fragile X syndrome
215	Tetralogy of Fallot
225	Congenital nephrogenic diabetes insipidus
226	Interstitial cystitis with Hunners ulcer
230	Alveolar hypoventilation syndrome
240	Phenylketonuria
274	Osteogenesis Imperfecta
278	Huge lymphatic malformation with cervicofacial lesion
299	Cystic fibrosis