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- W4387003054 abstract "To date, no approved drugs are available to treat the Zika virus (ZIKV) infection. Therefore, it is necessary to urgently identify potential drugs against the ZIKV infection. Here, the repurposing of 30 antiparasitic drugs against the NS2B-NS3 protease of the ZIKV has been carried out by using combined docking and molecular dynamics- (MD) simulations. Based on the docking results, 5 drugs, such as Amodiaquine, Primaquine, Paromomycin, Dichlorophene, and Ivermectin were screened for further analysis by MD simulations and free energy calculations. Among these drugs, Amodiaquine and Dichlorophen are found to produce the most stable complexes and possess relative binding free energies of about -44.3 ± 3.7 kcal/mol and -41.1 ± 5.3 kcal/mol respectively. Therefore, they would act as potent small-molecule inhibitors of the ZIKV protease.However, evaluations of biological and safety activities of these drugs against the ZIKV protease are required before their clinical use.Communicated by Ramaswamy H. Sarma." @default.
- W4387003054 created "2023-09-26" @default.
- W4387003054 creator A5006985610 @default.
- W4387003054 creator A5060210446 @default.
- W4387003054 date "2023-09-25" @default.
- W4387003054 modified "2023-10-01" @default.
- W4387003054 title "Repurposing of antiparasitic drugs against the NS2B-NS3 protease of the Zika virus" @default.
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- W4387003054 doi "https://doi.org/10.1080/07391102.2023.2255648" @default.
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