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Microbiology · Chemotherapeutic Antimicrobial Drugs

Antiviral drugs

Antiviral drugs are a group of medications designed to selectively inhibit various stages of viral replication inside the human body. The main difficulty in their development is that the pathogen uses the host cell's enzyme systems for reproduction, leaving extremely few specific targets for a safe medicinal strike.

Development complexityViruses are obligate intracellular parasites that completely subjugate the host cell.
Safety criterionDetermined by the chemotherapeutic index: the ratio of benefit (efficacy) to toxicity.
Frequent targetThe synthesis of viral nucleic acids is blocked by drugs from the abnormal nucleoside group.
Problem areasEffective agents for etiotropic therapy of enteroviruses and viral encephalitis are still lacking.
3 min readFor medical studentsUpdated 09/24/2026
Material prepared by WhiteCoat Pro editorial team based on platform study guidesReviewed by medical editor: Aulov A. A., general practitioner · 09/24/2026

Basic classification principles

Modern pharmacology relies on grouping antiviral agents based on their chemical structure and mechanism of action. Globally, all drugs are divided into four major categories:

  1. Chemotherapeutic drugs are synthetic molecules for etiotropic treatment that precisely target the pathogen.
  2. Interferons are endogenous human body proteins with natural antiviral activity.
  3. Interferon inducers are specific substances that stimulate the active production of the patient's own interferons.
  4. Immunomodulators are agents designed to correct and restore the immune response.

The main task of synthetic chemotherapeutic drugs is to selectively interrupt virion reproduction without significant damage to the healthy tissues of the host organism.

Targets and sites of action

The viral life cycle consists of several sequential stages. Chemical classes of drugs are tied to specific stages that they are capable of blocking:

  • Deproteinization (genome uncoating): the process is disrupted by adamantane derivatives.
  • Synthesis of 'early' viral proteins: blocked by guanidine.
  • Nucleic acid synthesis: genome replication is effectively halted by nucleoside analogues.
  • Synthesis of 'late' viral proteins: inhibited by peptide derivatives.
  • Assembly of new virions: a target for the action of thiosemicarbazone derivatives.
Test your knowledge on this topicAssignments from the Microbiology course bank — instant answers and explanations.

Abnormal nucleosides: the basis of therapy

This is the most extensive group of agents that disrupt nucleic acid synthesis. By incorporating into the chain, they make further replication impossible.

  • Azidothymidine (AZT): a baseline drug for the treatment of HIV infection (AIDS).
  • Acyclovir, vidarabine, idoxuridine: effective against herpes simplex viruses (types 1 and 2) and Varicella Zoster.
  • Ganciclovir and cytarabine: used for cytomegalovirus infection (ganciclovir also works against herpes type 1).
  • Ribavirin: has a broad spectrum, active against hepatitis C pathogens, Lassa fever, and respiratory syncytial virus.
  • Trifluridine: used in ophthalmology for keratitis of adenoviral and herpetic etiology.

Specific chemical classes

Depending on indications, other structural groups are used in clinical practice:

  • Adamantane derivatives. Target respiratory viruses. Amantadine and rimantadine are effective against influenza A; adapromine covers influenza types A and B; deitiforin has a complex action (influenza A, parainfluenza, RSV infection). An exception is tromantadine, which is used for herpes.
  • Synthetic amino acids. Amben and aminocaproic acid are prescribed for influenza, ARVI, parainfluenza, and RSV infection.
  • Pyrophosphate analogues. Foscarnet is used for severe systemic lesions: cytomegaly, hepatitis B, HIV, and herpes (types 1 and 6).
  • Thiosemicarbazone derivatives. Methisazone and marboran are historically important drugs used to combat smallpox.
  • Virucidal drugs. Topical agents (ointments, drops) that work against extracellular virions. Oxoline, tebrofen, and flurenal rescue in local forms of herpes, rhinitis, and viral keratitis.

Challenges of modern chemotherapy

Despite the colossal production volumes of antimicrobial agents, the physician faces two main problems. The first is the emergence of resistant strains of viruses that rapidly adapt to therapy and reduce treatment efficacy.

The second problem is the shortage of etiotropic drugs. While having a powerful base for therapy of HIV, hepatitis, and herpes, humanity still lacks reliable specific molecules for the treatment of a number of enteroviral infections and dangerous viral encephalitides.

How to memorize

Adamantane derivatives against respiratory infections are easy to remember by their roots: anti-influenza agents contain the parts 'mantadine' or 'promine' (amantadine, rimantadine, adapromine). But tromantadine is an exception; it treats herpes.

Class and exam questions

What is the main difference between chemotherapeutic drugs and interferons?

Chemotherapeutic drugs are artificially synthesized substances that purposefully target the stages of viral reproduction. Interferons, on the other hand, are endogenous (natural) proteins of the human body with a broad spectrum of antiviral activity.

What does the chemotherapeutic index show?

It shows the safety level of the drug. This is the mathematical ratio of its specific therapeutic efficacy to the degree of toxic impact on the host organism's cells.

Why is it difficult to create a universal drug against all viruses?

Most processes of transcription, translation, and assembly of viral particles are carried out not autonomously, but by the enzyme systems of the host cell itself. By destroying these processes, the drug is highly likely to kill the patient's living cell as well.

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What else to study on this topic

  • The molecular mechanism of abnormal nucleoside incorporation into the viral genome
  • Principles of action of endogenous interferons and inducers of their synthesis
  • The role of immunomodulators in the complex therapy of viral diseases
  • Causes of viral resistance development to chemotherapeutic drugs
  • Pharmacodynamics and specific features of topical virucidal agents' application

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