Table 6.8.
Antiviral Drugs
| Drug | Viruses | Chemical Type | Target |
|---|---|---|---|
| Vidarabine | Herpesviruses | Nucleoside analogue | Virus polymerase |
| Acyclovir | Herpes simplex (HSV) | Nucleoside analogue | Virus polymerase |
| Gancyclovir | Cytomegalovirus (CMV) | Nucleoside analogue | Virus polymerase (requires virus UL98 kinase for activation) |
| Nucleoside-analogue reverse transcriptase inhibitors (NRTI): zidovudine (AZT), didanosine (ddI), zalcitabine (ddC), stavudine (d4T), lamivudine (3TC) | Retroviruses (HIV) | Nucleoside analogue | Reverse transcriptase |
| Nonnucleoside reverse transcriptase inhibitors (NNRTI): nevirapine, delavirdine | Retroviruses: human immunodeficiency virus (HIV) | Nucleoside analogue | Reverse transcriptase |
| Protease inhibitors: saquinavir, ritonavir, indinavir, nelfinavir | HIV | Peptide analogue | HIV protease |
| Ribavirin | Broad-spectrum: hepatitis C virus (HCV), herpes simplex virus (HSV), measles, mumps, Lassa fever | Triazole carboxamide | RNA mutagen |
| Amantadine/rimantadine | Influenza A | Tricyclic amine | Matrix protein/hemagglutinin |
| Neuraminidase inhibitors: oseltamivir, zanamivir | Influenza A and B | Ethyl esther pro-drug requiring hydrolysis for conversion to the active carboxylate form | Neuraminidase |