Antiviral Flashcards

1
Q

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.

A
  • 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)
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2
Q

Name three agents licensed to treat Herpes Simplex Virus (HSV) and Varicella Zoster (VZV). Describe their mechanism of action.

A
  • 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.
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3
Q

List 4 main drugs used for influenza. Describe their mechanism of action.

A
  1. Oseltamivir: a neuraminidase inhibitor, preventing new viruses from emerging from infected cells.
  2. Zanamivir: a neuraminidase inhibitor, prophylaxis
    of both Influenza A and Influenza B.
  3. Amantadine: Resistance related to point mutations in the binding region of M.
  4. 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 β€œuncoated. Thus, no coating = no viral replication.
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4
Q

Describe the 5 main types/classes of anti-retrovirals for HIV. Include the site of action of each therapeutic class.

A
  1. Entry and Fusion Inhibitors
  2. The nucleoside reverse transcriptase inhibitors (NRTI)
  3. Nucleotide Inhibitors
  4. The non-nucleoside reverse transcriptase inhibitors (NNRTI)
  5. Protease Inhibitors
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5
Q

Describe HAART.

A

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).
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6
Q

Name two anti-viral drugs available for the treatment for CMV. Describe their mechanism of action.

A
  1. Cidofor: inhibits DNA polymerase.
  2. Fomivirsen: inhibits protein synthesis –
    therefore; inhibits viral replication.
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7
Q

Name two anti-viral drugs available for the treatment for Hepatitis B. Describe their mechanism of action.

A
  1. Lamivudine: suppresses HBV DNA replication.
  2. Adefor: a nucleotide analog that competitively inhibits Hepatitis B DNA polymerase and causes chain termination.
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8
Q

Name two anti-viral drugs available for the treatment for Hepatitis C. Describe their mechanism of action.

A
  1. Sofosbuvi: NS5B RNA polymerase inhibitor, NI (nucleoside inhibitor).
  2. Ledipasvir: NS5A replication complex inhibito
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