Table 3.
| Drug group | Drug name | Description |
|---|---|---|
| Nucleoside analogs | Sofosbuvir, MK-608 | • Inhibit Zika virus (ZIKV) replication in cellular assays • Efficacious in animal models |
| 2CMC, Ribavirin, Favipiravir, T1105 | • Showed antiviral activity in cell culture | |
| BCX4430, GS5734 | • Reduced mortality in ZIKV-infected mice • Currently in phase I and II clinical trials |
|
| Peptidomimetic agents | CN-716 | • Inhibit ZIKV protease in vitro, but only weakly inhibit viral replication • Due to safety reasons, may not translate as therapeutic option for pregnant women, but could be applied to other infected individuals |
| Adenosine analog | NITD008 | • Showed potent anti-ZIKV activity • Could serve as a reference inhibitor for future drug screen and discovery |
| Cyclin-dependent kinase inhibitor | PHA-690509 | • Showed inhibition of ZIKV replication of all three strains |
| Antimalaria | Chloroquine | • Reduces virus production, the number of infected cells, and cell death promoted by ZIKV infection without any cytotoxic effect • Promising candidate for ZIKV clinical trials • Can be safely administered to pregnant women since it is clinically approved |
| Anthelmintic | Bithionol | • Propagate by activating host caspases and inducing programmed cell death |
| Epigallocatechin gallate | • Natural compound found in food items, particularly green tea • It inhibits ZIKV entry into host cell |
|
| Interferon-inducible transmembrane proteins | • Inhibit the replication of a number of pathogenic viruses |