Antiviral Agents 
By:Jillian H. Davis
Department of Pharmacology, Howard University 
Viruses 
    * Obligate intracellular parasites
    * Consist of a core genome in a protein shell and some are surrounded by a lipoprotein
    * lack a cell wall and cell membrane
    * do not carry out metabolic processes
    * Replication depends on the host cell machinery
    * Steps for Viral Replication
Sites of Drug Action
Antiviral Agents 
Antiherpes Agents 
    * Acyclovir- prototype
    * Valacyclovir
    * Famciclovir
    * Penciclovir
    * Trifluridine
    * Vidarabine
Mechanism of Action    Acyclovir 
    * an acyclic guanosine derivative
    * Phosphorylated by viral thymidine kinase
    * Di-and tri-phosphorylated by host cellular enzymes
    * Inhibits viral DNA synthesis 
    * Alteration in viral thymidine kinase
    * Alteration in viral DNA polymerase
    * Cross-resistance with valacyclovir, famciclovir, and ganciclovir
Clinical Uses  Acyclovir 
    * Oral, IV, and Topical formulations
    * Cleared by glomerular filtration and tubular secretion
    * Uses:
          o Herpes Simplex Virus 1 and 2  (HSV)
          o Varicella-zoster virus (VZV)
    * Side Effects: nausea, diarrhea, headache, tremors, and delirium
Valacyclovir 
    * L-valyl ester of acyclovir
    * Converted to acyclovir when ingested
    * M.O.A.: same as acyclovir
    * Uses:
          o 1) recurrent genital herpes
          o 2) herpes zoster infections
    * Side Effects: nausea, diarrhea, and headache
Famciclovir 
    * Prodrug of penciclovir (a guanosine analog)
    * M.O.A.: same as acyclovir
    * does not cause chain termination
    * Uses: HSV-1, HSV-2, VZV, EBV, and hepatitis B
    * Side Effects: nausea, diarrhea, and headache
Trifluridine 
    * Trifluridine- fluorinated pyrimidine
          o inhibits viral DNA synthesis same as acyclovir
          o incorporates into viral and cellular DNA
          o Uses: HSV-1 and HSV-2 (topically)
Vidarabine 
    * An adenosine analog
    * inhibits viral DNA polymerase
    * incorporated into viral and cellular DNA
    * metabolized to hypoxanthine arabinoside
    * Side Effects: GI intolerance and myelosuppression
Anti-Cytomegalovirus Agents 
    * Gancyclovir
    * Valgancyclovir
    * Cidofovir
    * Foscarnet
    * Fomivirsen
Ganciclovir 
    * An acyclic guanosine analog
    * requires triphosphorylation for activation
    * monophosphorylation is catalyzed by a phosphotransferase in CMV and by thymidine kinase in HSV cells
    * M.O.A.: same as acyclovir
    * Uses: CMV*, HSV, VZV,and EBV
    * Side Effect: myelosuppression 
Valgancyclovir 
    * Monovalyl ester prodrug of gancyclovir
    * Metabolized by intestinal and hepatic esterases when administered orally
    * M.O.A.: same as gancyclovir
    * Uses: CMV*
    * Side Effect: myelosuppression
Cidofovir 
    * A cytosine analog
    * phosphorylation not dependent on viral enzymes
    * Uses: CMV*, HSV-1, HSV-2, VZV, EBV, HHV-6, adenovirus, and human papillomavirus
    * Side Effects: nephrotoxicity (prevented by admin. of probenecid)
    * Resistance: mutation in DNA polymerase gene
Foscarnet 
    * An inorganic pyrophosphate
    * inhibits viral DNA polymerase, RNA polymerase, and HIV reverse transcriptase
    * does not have to be phosphorylated
    * Uses: HSV, VZV, CMV, EBV, HHV-6, HBV, and HIV
    * Resistance due to mutations in DNA polymerase gene
    * Side Effects: hypo- or hypercalcemia and phosphotemia
Fomivirsen 
    * An oligonucleotide
    * M.O.A.: binds to mRNA and inhibits protein synthesis and viral replication
    * Uses: CMV retinitis
    * Side effects: iritis and increased intraocular pressure
Antiretroviral Agents 
1) Nucleoside Reverse Transcriptase Inhibitors (NRTIs) 
2) Nonnucleoside Reverse Transcriptase Inhibitors (NNRTIs) 
3)Protease inhibitors
Reverse Transcriptase Inhibitors 
    * Zidovudine (AZT)
    * Didanosine- causes pancreatitis*
    * Lamivudine- causes pancreatitis
    * Zalcitabine- causes peripheral neuropathy*
    * Stavudine- causes peripheral neuropathy*
    * Abacavir
Mechanism of Action    Zidovudine (AZT) 
    * A deoxythymidine analog
    * enters the cell via passive diffusion
    * must be converted to the triphosphate form by mammalian thymidine kinase
    * competitively inhibits deoxythymidine triphosphate for the reverse transcriptase enzyme
    * causes chain termination
Mechanism of Resistance    Zidovudine 
    * Due to mutations in the reverse transcriptase gene
    * more frequent after prolong therapy and in persons with HIV
Clinical Uses Zidovudine 
    * Available in IV and oral formulations
    * activity against HIV-1, HIV-2, and human T cell lymphotropic viruses
    * mainly used for treatment of HIV, decreases rate of progression and prolongs survival
    * prevents mother to newborn transmission of HIV
Side Effects Zidovudine 
    * Myelosuppression, including anemia and neutropenia
    * GI intolerance, headaches, and insomnia
Other NRTIs 
    * Didanosine- synthetic deoxy-adenosine analog; causes pancreatitis*
    * Lamivudine- cytosine analog
    * Zalcitabine- cytosine analog; causes peripheral neuropathy*
    * Stavudine- thymidine analog;causes peripheral neuropathy*
    * Abacavir- guanosine analog; more effective than the other agents; fatal hypersensitivity reactions can occur
Nucleotide Inhibitors 
    * Tenofovir
    * Adefovir
Nonnucleoside Reverse Transcriptase Inhibitors (NNRTIs) 
    * Nevirapine
    * Delavirdine
    * Efavirenz
Mechanism of Action NNRTIs 
Nonnucleoside Reverse Transcriptase Inhibitors (NNRTIs) 
Protease Inhibitors 
Indinavir and Ritonavir 
Saquinavir 
Nelfinavir and Amprenavir 
Fusion Inhibitors 
Anti-Hepatitis Agents 
Interferons 
Ribavirin 
Anti-Influenza Agents 
Amantadine and Rimantadine 
Zanamivir and Oseltamivir 
Antifungal Agents
Fungal Infections 
Systemic Antifungals 
Amphotericin B 
Flucytosine 
Azoles 
Differences in Azoles 
Mucocutaneous Antifungals 
Topical Antifungals 
Antiviral Agents.ppt
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