Oxtriphylline

Basic Information

Item Value
DrugBank ID DB01303
Evidence Level L5 (Computational Prediction)
Number of Predicted Indications 53

Predicted Indications (TxGNN)

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

# Indication Source
1 migraine disorder KG + DL
2 migraine with brainstem aura KG + DL
3 migraine with or without aura, susceptibility to KG + DL
4 atrophoderma vermiculata KG + DL
5 ulerythema ophryogenesis KG + DL
6 thrombotic disease KG + DL
7 hyperthyroidism KG + DL
8 sciatic neuropathy KG + DL
9 resistance to thyroid hormone due to a mutation in thyroid hormone receptor beta KG + DL
10 headache disorder KG + DL
11 Prinzmetal angina KG + DL
12 tendinitis KG + DL
13 fibromyalgia KG + DL
14 myositis fibrosa KG + DL
15 idiopathic granulomatous myositis KG + DL
16 trigeminal autonomic cephalalgia KG + DL
17 non-inflammatory vasculopathy KG + DL
18 angiodysplasia KG + DL
19 vein disease KG + DL
20 peripheral arterial disease KG + DL
21 inclusion body myositis KG + DL
22 amenorrhea (disease) KG + DL
23 venous thromboembolism KG + DL
24 fibrocartilaginous embolism KG + DL
25 anaphylaxis KG + DL
26 ischemic disease KG + DL
27 hyperthyroxinemia KG + DL
28 female breast carcinoma KG + DL
29 congenital renal artery stenosis KG + DL
30 vascular ectasia KG + DL
31 food-dependent exercise-induced anaphylaxis KG + DL
32 peripheral vascular disease KG + DL
33 keratosis pilaris KG + DL
34 vascular insufficiency disorder KG + DL
35 glossodynia KG + DL
36 coccygodynia KG + DL
37 rheumatoid arthritis KG + DL
38 scalp dermatosis KG + DL
39 Raynaud disease KG + DL
40 common cold KG + DL
41 anxiety KG + DL
42 interventricular septum aneurysm KG + DL
43 Laubry-Pezzi syndrome KG + DL
44 hereditary arterial and articular multiple calcification syndrome KG + DL
45 Pierre Robin syndrome associated with a chromosomal anomaly KG + DL
46 orofacial clefting syndrome KG + DL
47 Jeune syndrome situs inversus KG + DL
48 genetic syndromic Pierre Robin syndrome KG + DL
49 disorder involving pain KG + DL
50 partial deletion of the long arm of chromosome 7 KG + DL

(Showing top 50 of 53 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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