Structure via PubChem · Public domain (PubChem)
gliotoxin
Sign in to saveAlso known as Aspergillin
Gliotoxin is a sulfur-containing mycotoxin that belongs to a class of naturally occurring 2,5-diketopiperazines produced by several species of fungi, especially those of marine origin. It is the most prominent member of the epipolythiopiperazines, a large class of natural products featuring a diketopiperazine with di- or polysulfide linkage. These highly bioactive compounds have been the subject of numerous studies aimed at new therapeutics. Gliotoxin was originally isolated from Gliocladium fimbriatum, and was named accordingly. It is an epipolythiodioxopiperazine metabolite that is one of th
Chemical data
- Formula
- C13H14N2O4S2
- Molecular weight
- 326.4 g/mol
- IUPAC name
- (1R,7S,8S,11R)-7-hydroxy-11-(hydroxymethyl)-15-methyl-12,13-dithia-9,15-diazatetracyclo[9.2.2.01,9.03,8]pentadeca-3,5-diene-10,14-dione
- SMILES
- CN1C(=O)[C@]23CC4=CC=C[C@@H]([C@H]4N2C(=O)[C@]1(SS3)CO)O
- InChIKey
- FIVPIPIDMRVLAY-RBJBARPLSA-N
- XLogP
- -0.7
- Polar surface area
- 132 Ų
- H-bond donors
- 2
- H-bond acceptors
- 6
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Molecule type
- Small molecule
via ChEMBL · EBI
Research
904 papers- Gliotoxin Production and Self-Defense in Filamentous Fungi.Annual review of microbiology · 2025
- Gliotoxin--bane or boon?Environmental microbiology · 2016
- Progress in Gliotoxin Research.Molecules (Basel, Switzerland) · 2025
- Gliotoxin and related epipolythiodioxopiperazines.General pharmacology · 1996
- Gliotoxin, a natural product with ferroptosis inducing properties.Bioorganic chemistry · 2023
via PubMed
Wikidata facts
- Mass
- 326.039
Show 5 more facts
- chemical formula
- C₁₃H₁₄N₂O₄S₂
- canonical SMILES
- CN1C(=O)C23CC4=CC=CC(C4N2C(=O)C1(SS3)CO)O
- isomeric SMILES
- CN1C(=O)[C@]23CC4=CC=C[C@@H]([C@H]4N2C(=O)[C@]1(SS3)CO)O
- Commons category
- Gliotoxin
- subject has role
- immunosuppressive drug
via Wikidata · CC0
~15 min read
Encyclopedic overview
12 sectionsContents
- Occurrence
- Discovery
- Mechanism of action
- Biosynthesis
- Chemical synthesis
- Exposure and health effects
- Environmental exposure
- Clinical exposure
- Strategies for toxicity prevention
- Possible uses
- References
- Further reading
Gliotoxin is a sulfur-containing mycotoxin that belongs to a class of naturally occurring 2,5-diketopiperazines produced by several species of fungi, especially those of marine origin. It is the most prominent member of the epipolythiopiperazines, a large class of natural products featuring a diketopiperazine with di- or polysulfide linkage. These highly bioactive compounds have been the subject of numerous studies aimed at new therapeutics. Gliotoxin was originally isolated from Gliocladium fimbriatum, and was named accordingly. It is an epipolythiodioxopiperazine metabolite that is one of the most abundantly produced metabolites in human invasive Aspergillosis (IA).
==Occurrence== The compound is produced by human pathogens such as Aspergillus fumigatus, and also by species of Trichoderma and Penicillium. Gliotoxin has also been reported from yeasts of the genus Candida, but results from other studies have cast doubt on the production of this metabolite by Candida fungi. Gliotoxin is not produced by nonpathogenic A. fischeri although A.fischeri contains a gene cluster that is homologous to the gliotoxin gene cluster found in the pathogenic A. fumigatus. Gliotoxin contributes to the pathogenicity of opportunistic fungi by suppressing the immune system response of its host. Gliotoxin additionally possesses fungicidal and bacteriostatic properties, which indicates that it likely plays an important self defense role against bacteria and other fungi for the fungi that produce gliotoxin. Exposure of A. fumigatus to exogenous gliotoxin resulted in aberrant protein expression, especially in those strains that lacked the self-protection protein GliT. There is additional evidence for differential gliotoxin sensitivities amongst fungi including Aspergillus flavus, Fusarium graminearum, and Aspergillus oryzae.
Excerpted from Wikipedia’s “gliotoxin” article, available under the CC BY-SA 4.0 licence.