Table 3 Protein targets for drug repositioning. E. granulosus H-PSCs up-regulated proteins for which there are available inhibitory drugs previously used for the treatment of different infections/diseases.
From: Unraveling oxidative stress response in the cestode parasite Echinococcus granulosus
Target | Drug | Mechanism of action | Disease or pathogen treatable by the drug | Ref |
|---|---|---|---|---|
Glycerol-3-phosphate dehydrogenase | Anacardic acids | Non-competitive enzyme inhibition | Tumors and Bacterial pathogens | |
Carbonyl reductase | Biphenyl compounds | Enzyme inhibition | Breast cancer | |
Cathepsin D | Amprenavira, Indinavira, Lopinavira, Nelfinavira, Ritonavira, Saquinavira | Enzyme inhibition | Human Immunodeficiency Virus Trypanosomatids: Leishmania species and T. cruzi | |
Estradiol 17-beta dehydrogenase | Steroidal STX1040 and non-steroidal PBRM | Enzyme inhibition | Breast cancer | |
Glutathione-S-transferase | Ethacrynic acid analoguesa | Enzyme inhibition | Cancers | |
Glutathione analogues: ezatiostat (TLK199) | Myelodysplastic syndrome | |||
Proteasome subunits | Bortezomiba | Inhibition of p53 degradation? | Multiple myeloma | |
Epoxomicin | Proteasome inhibition | Babesia divergens | ||
Carmaphycin B analogs | Proteasome inhibition | Plasmodium falciparum |