Target intelligence / Profile preview

Skin fungi (N/A)

Target
N/A
Molecular classification
Other
01

Overview

Skin fungi refers to a diverse group of microorganisms, including dermatophytes (such as Trichophyton, Microsporum, and Epidermophyton), yeasts (such as Candida and Malassezia), and molds that colonize or infect the human skin, hair, and nails (StatPearls, 2023). These organisms are clinically significant due to their ability to invade keratinized tissues, causing infections such as tinea pedis, onychomycosis, and candidiasis (NIH, 2022). While not a single molecular target, they are the focus of antifungal therapy, which aims to disrupt essential fungal processes such as ergosterol biosynthesis or cell wall construction (PubMed, 2021). Common clinical manifestations include athlete's foot, ringworm, and onychomycosis (Mayo Clinic, 2023). Effective management involves topical or systemic antifungal drugs, though rising resistance and potential systemic side effects like hepatotoxicity remain significant therapeutic challenges (Journal of Fungi, 2022). The primary molecular targets within these fungi include squalene epoxidase, targeted by allylamines, and lanosterol 14-alpha-demethylase, targeted by azoles. Disruption of these enzymes leads to the depletion of ergosterol, a critical component of the fungal cell membrane, resulting in increased membrane permeability and cell death. Additionally, some agents target the fungal cell wall by inhibiting 1,3-beta-glucan synthase.

Other names
DermatophytesCutaneous fungiSkin mycobiotaKeratinophilic fungiTinea pathogens
02

Mechanism of action

Antifungal agents typically target the fungal cell membrane or cell wall. Azoles inhibit lanosterol 14-alpha-demethylase (CYP51), preventing the conversion of lanosterol to ergosterol. Allylamines like terbinafine inhibit squalene epoxidase, leading to squalene accumulation and ergosterol deficiency. Echinocandins inhibit 1,3-beta-glucan synthase, disrupting the structural integrity of the fungal cell wall.

03

Biological functions

Keratin degradationColonization of epithelial surfacesFungal metabolismNutrient cycling
04

Disease associations

InfectionInflammationDermatophytosisCandidiasisTinea corporisOnychomycosisPityriasis versicolor
05

Safety considerations

Antifungal resistanceHepatotoxicity with systemic useDrug-drug interactions via CYP450 inhibitionLocal skin irritation and hypersensitivity
06

Interacting drugs

Terbinafine

8 more in the full profile.

07

Biomarkers

Potassium hydroxide (KOH) preparationFungal cultureFungal DNA PCRWood's lamp fluorescence

Beyond the preview

Go deeper on Skin fungi (N/A).

Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.

Drug pipeline

Full profile access

Explore the programs pursuing this target and their development progress.

  • Drug candidates
  • Developers
  • Development stage

Clinical trials

Full profile access

Follow the clinical studies evaluating therapies directed at this target.

  • Trial design
  • Status
  • Readouts

Competitive landscape

Full profile access

Compare approaches across drug candidates, modalities, and indications.

  • Programs
  • Modalities
  • Indications

Literature & evidence

Full profile access

Investigate the research and source evidence behind target biology and development.

  • Publications
  • Sources
  • Analysis

Patents

Full profile access

Explore patent activity around therapies and technologies addressing this target.

  • Patents
  • Assignees
  • Technologies

Research & analysis

Full profile access

Connect target biology, drug development, and emerging evidence in your research.

  • Biology
  • Development news
  • Analysis

Bring the full picture into focus.

See how Gosset can support your research on Skin fungi (N/A).

Explore the full profile

Gosset Free

Get started with Gosset.

Enter your work email and we’ll be in touch with next steps.

Work email preferred.

Book a call