Antiviral drug

From Citizendium
Revision as of 03:49, 23 February 2008 by imported>David E. Volk
Jump to navigation Jump to search
This article is a stub and thus not approved.
Main Article
Discussion
Related Articles  [?]
Bibliography  [?]
External Links  [?]
Citable Version  [?]
Catalogs [?]
 
This editable Main Article is under development and subject to a disclaimer.

An antiviral drug, or antiviral agent, is a compound that interfers with the replication cycle of viruses. They can be divided into three non-exclusive categories: protease inhibitors, anti-metabolites and reverse transcriptase inhibitors, based on the ways in which they disrupt viral replication cycles. While antiviral drugs are intended for systemic use by ingestion or injection of the drug, virucides are used exclusively on objects and surfaces and, when possible, topically.

Protease inhibitors, as the name suggests, inhibit the function of protease enzymes created by viruses. The DNA or RNA in viruses are coded to produce large polyproteins, which need to be cleaved into smaller functional proteins by viral proteases before infectious, mature virus particles can be formed. For example, West Nile virus and Dengue virus produce a single polyprotein that must be cleaved into ten separate proteins.

Anti-metabolites, which are often nucleoside analogs that disrupt the replication or translation of viral DNA or RNA upon their incorporation or reverse transcriptase inhibitors (RTIs). Some drugs fit 2 or 3 of these categories. More information about these drugs can be found in their respective article pages.

List of protease inhibitors


antimetabolites and RT inhibitors

  • Abacavir - a powerful nucleoside analog reverse transcriptase inhibitor used to treat HIV and AIDS.
  • Adefovir Dipivoxil - nucleotide analog reverse transcriptase inhibitor (ntRTI) hepatitis B treatment.
  • Delavirdine - A non-nucleoside reverse transcriptase (RT) inhibitor active against HIV-1.
  • Didanosine - a dideoxynucleoside prevents phosphodiester bonds; it is an inhibitor of HIV replication.
  • Entecavir - a guanosine analog for treatment of hepatitis B.
  • Efavirenz - a non-nucleoside reverse transcriptase inhibitor (NNRTI)used to treat HIV.
  • Foscarnet - inorganic pyrophosphate analog treats CMV retinitis, herpesviruses, and HIV.
  • Idoxuridine - a deoxyuridine analog that inhibits viral DNA synthesis.
  • Lamivudine - An RT inhibitor, zalcitabine analog used to treat HIV disease
  • Nevirapine - a non-nucleoside reverse transcriptase inhibitor used to treate HIV/AIDS
  • Oseltamivir (Tamaflu) - inhibits neuraminidase in the treatment of influenza infections.
  • Ribavirin - a nucleoside antimetabolite used against both RNA and DNA viruses.
  • Rimantadine - a cyclic amine derivate of adamantane, inhibits replication of influenza A, but not B.
  • Stavudine - A dideoxynucleoside analog, inhibits reverse transcriptase in HIV treatment.
  • Tenofovir - a nucleoside analog, reverse transcriptase inhibitor (nRTI),
  • Vidarabine - purine nucleoside analogue for the treatment of chickenpox (varicella) and herpes viruses
  • Zalcitabine - a dideoxynucleoside, prevents phosphodiester bonds, a potent inhibitor of HIV replication.
  • Zanamivir - a guanido-neuraminic acid used to inhibit neuraminidase, inhibits influenza.
  • Zidovudine - A dideoxynucleoside, prevents phosphodiester bonds, a potent inhibitor of HIV replication.

External Links

Drug Bank at http://www.drugbank.ca/cat_browse.htm#subC10