Sacubitril

Basic Information

Item Value
DrugBank ID DB09292
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 brain small vessel disease 1 with or without ocular anomalies KG + DL
2 autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome KG + DL
3 diabetic nephropathy KG + DL
4 rheumatoid arthritis KG + DL
5 hemoglobinopathy KG + DL
6 sclerosing cholangitis KG + DL
7 colobomatous microphthalmia-rhizomelic dysplasia syndrome KG + DL
8 homozygous familial hypercholesterolemia KG + DL
9 partial deletion of the short arm of chromosome 16 KG + DL
10 beta-thalassemia with other manifestations KG + DL
11 blindness (disorder) KG + DL
12 pyropoikilocytosis, hereditary KG + DL
13 migraine disorder KG + DL
14 migraine with brainstem aura KG + DL
15 brachydactyly-syndactyly syndrome KG + DL
16 pyruvate kinase deficiency of red cells KG + DL
17 hemolytic anemia due to glucophosphate isomerase deficiency KG + DL
18 gout KG + DL
19 postmenopausal osteoporosis KG + DL
20 myocardial infarction KG + DL
21 chronic renal failure syndrome KG + DL
22 bone Paget disease KG + DL
23 pregnancy associated osteoporosis KG + DL
24 Prinzmetal angina KG + DL
25 hyperthyroidism KG + DL
26 chronic kidney disease KG + DL
27 resistance to thyroid hormone due to a mutation in thyroid hormone receptor beta KG + DL
28 intracerebral hemorrhage KG + DL
29 congestive heart failure KG + DL
30 Worth syndrome KG + DL
31 autosomal dominant neovascular inflammatory vitreoretinopathy KG + DL
32 septal myocardial infarction KG + DL
33 acute coronary syndrome KG + DL
34 posterolateral myocardial infarction KG + DL
35 posteroinferior myocardial infarction KG + DL
36 myocardial infarction (disease) KG + DL
37 primary hereditary glaucoma KG + DL
38 hypertensive disorder KG + DL
39 open-angle glaucoma KG + DL
40 end stage renal failure KG + DL
41 pulmonary hypertension with unclear multifactorial mechanism KG + DL
42 pulmonary hypertension owing to lung disease and/or hypoxia KG + DL
43 malignant hypertensive renal disease KG + DL
44 malignant renovascular hypertension KG + DL
45 succinyl-CoA:3-ketoacid CoA transferase deficiency KG + DL
46 hypotrichosis simplex of the scalp KG + DL
47 methemoglobinemia, alpha type KG + DL
48 hypoalphalipoproteinemia KG + DL
49 chronic pulmonary heart disease KG + DL
50 coronary stenosis 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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