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No.
Drug (Description in trials)
DrugBank
KEGG DRUG
KEGG GENES
KEGG PATHWAY
Disease ID
1
3,4-DIAMINOPYRIDINE
-
-
-
-
[2]
12
12
,
13
💬
1. 3,4-DIAMINOPYRIDINE
×
Disease ID
Name
12
Congenital myasthenic syndrome
13
Multiple sclerosis/Neuromyelitis optica
2
Albuterol
[1]
Salbutamol
Salbutamol
[1]
Albuterol
Albuterol
💬
2. Albuterol
×
Name
Other Names
Albuterol
Albuterol (USP)
Salbutamol
Proventil (TN)
[1]
ADRB2
ADRB2
💬
2. Albuterol
×
Name
Full Name
ADRB2
adrenoceptor beta 2
[9]
Adrenergic signaling in cardiomyocytes
Adrenergic signaling in cardiomyocytes
,
Calcium signaling pathway
,
Chemical carcinogenesis - receptor activation
,
Neuroactive ligand-receptor interaction
,
Regulation of lipolysis in adipocytes
,
Renin secretion
,
Salivary secretion
,
cAMP signaling pathway
,
cGMP-PKG signaling pathway
💬
[7]
12
12
,
13
,
86
,
89
,
113
,
256
,
299
💬
2. Albuterol
×
Disease ID
Name
12
Congenital myasthenic syndrome
13
Multiple sclerosis/Neuromyelitis optica
86
Pulmonary arterial hypertension
89
Lymphangioleiomyomatosis
113
Muscular dystrophy
256
Muscle glycogenosis
299
Cystic fibrosis
3
Amifampridine
[1]
Amifampridine
Amifampridine
[1]
Amifampridine
Amifampridine
💬
3. Amifampridine
×
Name
Other Names
Amifampridine
Amifampridine (USAN/INN)
Ruzurgi (TN)
[4]
KCNA4
KCNA4
,
KCNC3
,
KCND2
,
KCND3
💬
3. Amifampridine
×
Name
Full Name
KCNA4
potassium voltage-gated channel subfamily A member 4
KCNC3
potassium voltage-gated channel subfamily C member 3
KCND2
potassium voltage-gated channel subfamily D member 2
KCND3
potassium voltage-gated channel subfamily D member 3
[4]
Cortisol synthesis and secretion
Cortisol synthesis and secretion
,
Cushing syndrome
,
Serotonergic synapse
,
Spinocerebellar ataxia
💬
[3]
3
3
,
11
,
12
💬
3. Amifampridine
×
Disease ID
Name
3
Spinal muscular atrophy
11
Myasthenia gravis
12
Congenital myasthenic syndrome
4
Amifampridine Phosphate
[2]
Amifampridine
Amifampridine
,
Phosphate ion
[1]
Amifampridine
Amifampridine
💬
4. Amifampridine Phosphate
×
Name
Other Names
Amifampridine
Amifampridine (USAN/INN)
Ruzurgi (TN)
[4]
KCNA4
KCNA4
,
KCNC3
,
KCND2
,
KCND3
💬
4. Amifampridine Phosphate
×
Name
Full Name
KCNA4
potassium voltage-gated channel subfamily A member 4
KCNC3
potassium voltage-gated channel subfamily C member 3
KCND2
potassium voltage-gated channel subfamily D member 2
KCND3
potassium voltage-gated channel subfamily D member 3
[4]
Cortisol synthesis and secretion
Cortisol synthesis and secretion
,
Cushing syndrome
,
Serotonergic synapse
,
Spinocerebellar ataxia
💬
[3]
3
3
,
11
,
12
💬
4. Amifampridine Phosphate
×
Disease ID
Name
3
Spinal muscular atrophy
11
Myasthenia gravis
12
Congenital myasthenic syndrome
5
Phosphate
[1]
Phosphate ion
Phosphate ion
-
-
-
[32]
2
2
,
3
,
6
,
11
,
12
,
13
,
28
,
36
,
46
,
49
,
51
,
53
,
60
,
62
,
65
,
70
,
78
,
81
,
83
,
90
,
96
,
97
,
164
,
235
,
238
,
256
,
276
,
283
,
284
,
285
,
286
,
299
💬
5. Phosphate
×
Disease ID
Name
2
Amyotrophic lateral sclerosis
3
Spinal muscular atrophy
6
Parkinson disease
11
Myasthenia gravis
12
Congenital myasthenic syndrome
13
Multiple sclerosis/Neuromyelitis optica
28
Systemic amyloidosis
36
Epidermolysis bullosa
46
Malignant rheumatoid arthritis
49
Systemic lupus erythematosus
51
Scleroderma
53
Sjogren syndrome
60
Aplastic anemia
62
Paroxysmal nocturnal hemoglobinuria
65
Primary immunodeficiency
70
Spinal stenosis
78
Hypopituitarism
81
Congenital adrenal hyperplasia
83
Addison disease
90
Retinitis pigmentosa
96
Crohn disease
97
Ulcerative colitis
164
Oculocutaneous albinism
235
Hypoparathyroidism
238
Vitamin D-resistant rickets
256
Muscle glycogenosis
276
Achondroplasia
283
Acquired pure red cell aplasia
284
Diamond-Blackfan anemia
285
Fanconi anemia
286
Hereditary sideroblastic anemia
299
Cystic fibrosis