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Related Concept Videos

Antifungal Agents01:15

Antifungal Agents

Amphotericin B is a broad-spectrum antifungal agent that exploits structural differences between fungal and mammalian cell membranes. Its amphipathic structure—featuring a hydrophobic polyene-lactone ring and a hydrophilic region containing mycosamine and carboxylic acid groups—enables selective binding to ergosterol, a sterol predominantly found in fungal plasma membranes. This selective interaction underlies the drug’s antifungal activity, although weak binding to cholesterol contributes to...
Anthelminthic Agents01:15

Anthelminthic Agents

Anthelmintic drugs differ significantly from antiparasitic therapies targeting protozoa, primarily due to differences in parasite biology. Whereas most protozoal treatments act on proliferating cells, anthelmintics are typically directed against mature, nonproliferative helminths. The therapeutic approach considers the helminth's reliance on neuromuscular coordination, glucose metabolism, and microtubular integrity for survival, reproduction, and localization within the host. Most anthelmintics...
Antiprotozoal Agents01:21

Antiprotozoal Agents

Leishmaniasis is a widespread parasitic disease caused by several Leishmania species. It affects millions of people each year and remains a major public health problem in endemic regions. First-line treatment relies on pentavalent antimonials, including meglumine antimoniate and sodium stibogluconate. Even so, how these drugs work has not been fully clear, especially their interaction with parasite-specific biochemical pathways. One key target is trypanothione reductase (TR), an enzyme that...
Antimicrobial Effectiveness01:28

Antimicrobial Effectiveness

The effectiveness of antimicrobial agents depends on various factors influencing their ability to eliminate microbial populations. Larger microbial populations require more time for complete eradication, emphasizing the importance of population size analysis when evaluating antimicrobial efficacy.Microbial resistance to antimicrobial agents varies significantly. Highly resilient microorganisms include endospores, gram-negative bacteria, and non-enveloped viruses, while prions are exceptionally...
Cryptococcal Meningitis01:27

Cryptococcal Meningitis

Cryptococcal meningitis is a life-threatening opportunistic infection predominantly associated with HIV/AIDS, accounting for over 100,000 deaths annually worldwide. However, it also affects individuals with other forms of immunosuppression, including those undergoing immunosuppressive therapy, organ transplant recipients, patients with innate immunodeficiencies, and individuals with hematological disorders. The infection is caused mainly by Cryptococcus neoformans and Cryptococcus gattii,...
Antiviral Nucleoside Inhibitors01:22

Antiviral Nucleoside Inhibitors

Antiviral Nucleoside InhibitorsAntiviral nucleoside inhibitors are structural analogs of natural nucleosides that interfere with viral DNA or RNA synthesis. These compounds selectively target viral polymerases due to their resemblance to host nucleosides, thereby disrupting viral genome replication.Mechanism of Acyclovir ActionAcyclovir is a guanosine analog with a three-carbon acyclic side chain. It selectively targets herpes simplex virus type 1 (HSV-1), herpes simplex virus type 2 (HSV-2),...

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Related Experiment Video

Updated: Jul 11, 2026

Broth Microdilution In Vitro Screening: An Easy and Fast Method to Detect New Antifungal Compounds
08:54

Broth Microdilution In Vitro Screening: An Easy and Fast Method to Detect New Antifungal Compounds

Published on: February 14, 2018

Recent advances in antifungal agents.

Tamás Lóránd1, Béla Kocsis

  • 1Department of Biochemistry and Medical Chemistry, University Pécs, Faculty of Medicine, H-7624 Pécs, Szigeti út 12., Hungary. tamas.lorand@aok.pte.hu

Mini Reviews in Medicinal Chemistry
|September 28, 2007
PubMed
Summary

New antifungal drugs are crucial due to rising drug resistance and immunocompromised patients. This review covers novel triazoles, echinocandins, nikkomycins, and sordarin derivatives targeting various fungal pathways.

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Last Updated: Jul 11, 2026

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Area of Science:

  • Medical Mycology
  • Infectious Diseases
  • Pharmacology

Background:

  • Increasing incidence of invasive fungal infections.
  • Emergence of antifungal resistance in opportunistic fungi.
  • Growing population of immunocompromised patients (e.g., AIDS, transplant, cancer).

Purpose of the Study:

  • To review novel antifungal agents and their mechanisms of action.
  • To highlight advancements in antifungal drug development.
  • To address the need for new treatments against resistant fungal pathogens.

Main Methods:

  • Literature review of new antifungal classes and agents.
  • Discussion of mechanisms targeting ergosterol, 1,3-beta-glucan, chitin, and protein synthesis.
  • Comparative analysis of novel agents against existing antifungals.

Main Results:

  • Novel triazoles (voriconazole, posaconazole, ravuconazole) inhibit ergosterol synthesis, overcoming limitations of older azoles.
  • Echinocandins (caspofungin, anidulafungin, micafungin) target 1,3-beta-glucan synthase.
  • Nikkomycins show activity against dimorphic fungi, and sordarin derivatives show promise against Candida and Pneumocystis.

Conclusions:

  • New antifungal agents offer improved efficacy and broader spectrum activity.
  • Targeting diverse fungal pathways is key to overcoming resistance.
  • Continued development of novel antifungals is essential for managing invasive mycoses.