Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Antiviral sulfonamide derivatives.

Claudiu T Supuran1, Alessio Innocenti, Antonio Mastrolorenzo

  • 1Università degli Studi di Firenze, Dipartimento di Chimica, Laboratorio di Chimica Bioinorganica, Via della Lastruccia, 3, Rm. 188, I-50019 Sesto Fiorentino, Florence, Italy. claudiu.supuran@unifi.it

Mini Reviews in Medicinal Chemistry
|February 18, 2004
PubMed
Summary

Sulfonamide derivatives show significant antiviral potential, including against HIV. Research focuses on novel compounds targeting viral enzymes and replication mechanisms for improved efficacy and reduced toxicity.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Plasmatic carbonic anhydrase IX as a diagnostic marker for clear cell renal cell carcinoma.

Journal of enzyme inhibition and medicinal chemistry·2017
Same author

Coral Carbonic Anhydrases: Regulation by Ocean Acidification.

Marine drugs·2016
Same author

Development and biological evaluation of ⁹⁹mTc-sulfonamide derivatives for in vivo visualization of CA IX as surrogate tumor hypoxia markers.

European journal of medicinal chemistry·2014
Same author

Anion inhibition studies of the α-carbonic anhydrase from the protozoan pathogen Trypanosoma cruzi, the causative agent of Chagas disease.

Bioorganic & medicinal chemistry·2013
Same author

The extremo-α-carbonic anhydrase from the thermophilic bacterium Sulfurihydrogenibium azorense is highly inhibited by sulfonamides.

Bioorganic & medicinal chemistry·2013
Same author

7-Substituted-sulfocoumarins are isoform-selective, potent carbonic anhydrase II inhibitors.

Bioorganic & medicinal chemistry·2013

Area of Science:

  • Medicinal Chemistry
  • Antiviral Drug Discovery
  • Pharmacology

Background:

  • Sulfonamides are a versatile drug class with diverse pharmacological activities.
  • Structurally novel sulfonamide derivatives have demonstrated potent antiviral effects.
  • Existing antiviral therapies often face challenges like toxicity and drug resistance.

Purpose of the Study:

  • To review recent advancements in sulfonamide-based antiviral agents.
  • To highlight sulfonamide derivatives targeting various stages of viral replication.
  • To explore strategies for developing less toxic and more effective antiviral compounds.

Main Methods:

  • Literature review of recent sulfonamide derivatives with antiviral activity.
  • Analysis of sulfonamide structures in clinically used and investigational antiviral drugs.

Related Experiment Videos

  • Examination of mechanisms of action, including enzyme inhibition and viral protein targeting.
  • Main Results:

    • Sulfonamide moieties are present in clinically relevant HIV protease inhibitors (e.g., amprenavir) and compounds in trials (e.g., tipranavir).
    • Numerous novel sulfonamide derivatives are under development for antiviral applications.
    • Compounds incorporating primary sulfonamide groups effectively inhibit retroviral replication by targeting zinc finger proteins.

    Conclusions:

    • Sulfonamides represent a promising scaffold for developing novel antiviral drugs, particularly against HIV.
    • Targeting viral enzymes and essential protein functions with sulfonamide derivatives offers a viable strategy.
    • Continued research into sulfonamide chemistry is crucial for overcoming antiviral drug resistance and toxicity.