Nicorandil

Basic Information

Item Value
DrugBank ID DB09220
Evidence Level L5 (Computational Prediction)
Number of Predicted Indications 100

Predicted Indications (TxGNN)

The following are potential new indications predicted by the TxGNN model. Higher scores indicate higher predicted relevance.

# Indication Source
1 benign prostatic hyperplasia (disease) KG + DL
2 alopecia KG + DL
3 hypotrichosis simplex of the scalp KG + DL
4 congenital hypotrichosis milia KG + DL
5 diffuse alopecia areata KG + DL
6 osteoarthritis susceptibility KG + DL
7 osteoarthritis KG + DL
8 acromesomelic dysplasia, Hunter-Thompson type KG + DL
9 brachyolmia KG + DL
10 brachyolmia-amelogenesis imperfecta syndrome KG + DL
11 hypertensive disorder KG + DL
12 myosclerosis KG + DL
13 pseudoachondroplasia KG + DL
14 pulmonary hypertension KG + DL
15 pulmonary hypertension owing to lung disease and/or hypoxia KG + DL
16 pulmonary hypertension with unclear multifactorial mechanism KG + DL
17 arthropathy KG + DL
18 malignant hypertensive renal disease KG + DL
19 malignant renovascular hypertension KG + DL
20 Braddock syndrome KG + DL
21 kyphoscoliotic heart disease KG + DL
22 rheumatoid arthritis KG + DL
23 chronic pulmonary heart disease KG + DL
24 female breast carcinoma KG + DL
25 subarachnoid hemorrhage (disease) KG + DL
26 prostate calculus KG + DL
27 pseudopelade of Brocq KG + DL
28 hemoglobinopathy KG + DL
29 congestive heart failure KG + DL
30 gout KG + DL
31 androgenetic alopecia KG + DL
32 headache disorder KG + DL
33 peripheral vascular disease KG + DL
34 acute pulmonary heart disease KG + DL
35 Prinzmetal angina KG + DL
36 migraine disorder KG + DL
37 colobomatous microphthalmia-rhizomelic dysplasia syndrome KG + DL
38 pulmonary hypertension, primary, autosomal recessive KG + DL
39 myocardial infarction KG + DL
40 trigeminal autonomic cephalalgia KG + DL
41 beta-thalassemia with other manifestations KG + DL
42 partial deletion of the short arm of chromosome 16 KG + DL
43 brachydactyly-syndactyly syndrome KG + DL
44 migraine with brainstem aura KG + DL
45 pyropoikilocytosis, hereditary KG + DL
46 idiopathic granulomatous myositis KG + DL
47 myositis fibrosa KG + DL
48 tendinitis KG + DL
49 nephrogenic syndrome of inappropriate antidiuresis KG + DL
50 hemolytic anemia due to glucophosphate isomerase deficiency KG + DL

(Showing top 50 of 100 predictions)

Disclaimer

These predictions are for research purposes only and do not constitute medical advice. Clinical validation is required before any clinical application.


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