Antiviral Flashcards
There are various steps in the virus replication cycle (entry, replication etc.). Give examples of anti-viral drugs targeting each step of virus replication. Also include the name of the virus each drug is effective against.
- Viral Insertion
- Penetration
- Uncoating: Amantadine Rimantidine (Inlfuenza A)
- Early Protein Synthesis: Fomivirsen (CMV)
- Nucleic Acid Synthesis: Purine and Pyrimidine Analogs, reverse transciptase inhibitors (HIV)
- Late Protein Synthesis/Processing: Methizone (variola), Protease Inhibitors (HIV)
- Packaging and Assembly: Rifampin (vaccinia)
- Release: Neuraminidase Inhibitors (Influenza)
Name three agents licensed to treat Herpes Simplex Virus (HSV) and Varicella Zoster (VZV). Describe their mechanism of action.
- Acyclovir IV and PO and Topical: converts into ACV-TP. It inhibits viral DNA polymerase.
- Valacyclovir PO: converted to acyclovir, then ACV-TP. It inhibits viral DNA polymerase.
- Famciclovir PO: converts into penciclovir. It inhibits viral DNA polymerase.
List 4 main drugs used for influenza. Describe their mechanism of action.
- Oseltamivir: a neuraminidase inhibitor, preventing new viruses from emerging from infected cells.
- Zanamivir: a neuraminidase inhibitor, prophylaxis
of both Influenza A and Influenza B. - Amantadine: Resistance related to point mutations in the binding region of M.
- Rimantadine: Resistance related to point mutation in the transmembrane domain of M.
- Both: antagonizes the viral protein M2, which is
needed for the viral particle to become βuncoated. Thus, no coating = no viral replication.
Describe the 5 main types/classes of anti-retrovirals for HIV. Include the site of action of each therapeutic class.
- Entry and Fusion Inhibitors
- The nucleoside reverse transcriptase inhibitors (NRTI)
- Nucleotide Inhibitors
- The non-nucleoside reverse transcriptase inhibitors (NNRTI)
- Protease Inhibitors
Describe HAART.
is a medication regimen used to manage and treat human immunodeficiency virus type 1 (HIV-1), by suppressing plasma viral load.
- Combination treatment is essential: 2 NRTIs + 1 NNRTI (Z+L+Efavirenz) or 2 NRTIs + 1 or 2 Protease inhibitors (Z+L+lopinavir).
Name two anti-viral drugs available for the treatment for CMV. Describe their mechanism of action.
- Cidofor: inhibits DNA polymerase.
- Fomivirsen: inhibits protein synthesis β
therefore; inhibits viral replication.
Name two anti-viral drugs available for the treatment for Hepatitis B. Describe their mechanism of action.
- Lamivudine: suppresses HBV DNA replication.
- Adefor: a nucleotide analog that competitively inhibits Hepatitis B DNA polymerase and causes chain termination.
Name two anti-viral drugs available for the treatment for Hepatitis C. Describe their mechanism of action.
- Sofosbuvi: NS5B RNA polymerase inhibitor, NI (nucleoside inhibitor).
- Ledipasvir: NS5A replication complex inhibito