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Table 4 Therapeutic information of the drugs assigned to the baseline class that were scored highest by the malaria model a

From: Exploiting large-scale drug-protein interaction information for computational drug repurposing

Generic name

Score

Information from DrugBankb

Information from other sources

Dexamethasone

22.1

An anti-inflammatory 9-fluoro-glucocorticoid.

Dexamethasone was reported to have a dramatic life-saving effect on people with cerebral malaria [44]. However, two subsequent placebo-controlled clinical trials failed to demonstrate clinical benefit [45, 46].

Verapamil

21.5

A calcium channel blocker for hypertension, angina, and cluster headache prophylaxis.

A 1995 study [48] reported that verapamil reverses chloroquine resistance in the malaria parasite.

Quercetin

18.9

A flavonol found in plants, antioxidant.

A 2012 study [47] reported that quercetin had antiplasmodial activity.

Miconazole

16.5

An imidazole antifungal agent.

Many studies [3943] have reported antimalarial activities of antifungal azole compounds.

Clotrimazole

15.9

An imidazole derivative with a broad spectrum of antimycotic activity.

Many studies [3943] have reported antimalarial activities of azoles, including clotrimazole [43].

Cimetidine

15.5

For acid-reflux disorders (GERD), peptic ulcer disease, heartburn, and acid indigestion.

A 1997 study [49] reported synergism of cimetidine with antimalarial agents. It is ineffective when used alone.

Ketoconazole

15.2

For systemic fungal infections.

Many studies [3943] have reported antimalarial activities of azoles, including ketoconazole [41].

Nifedipine

14.9

A calcium channel blocker for angina, hypertension, and Raynaud's phenomenon.

 

Tamoxifen

14.4

For breast cancer.

 

Clobetasol

14.4

For corticosteroid-responsive dermatoses of the scalp.

 
  1. aThe model was developed with all 11 antimalarial drugs in the positive class; the remaining compounds were potential repurposing candidates in the baseline class.
  2. bRef. [26].