gliotoxin

chemical compound
ChemicalSubstance type_of_chemical_entity Q413364
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gliotoxin

Summary

gliotoxin is a type of chemical entity[1]. gliotoxin has Wikipedia articles in 9 language editions, a strong signal of global cultural recognition.[2]

Key Facts

  • gliotoxin's instance of is recorded as type of chemical entity[3].
  • gliotoxin's canonical SMILES is recorded as CN1C(=O)C23CC4=CC=CC(C4N2C(=O)C1(SS3)CO)O[4].
  • gliotoxin's chemical formula is recorded as C₁₃H₁₄N₂O₄S₂[5].
  • gliotoxin is a type of biogenic 2,5-diketopiperazine[6].
  • gliotoxin is part of gliotoxin metabolic process[7].
  • gliotoxin is part of gliotoxin catabolic process[8].
  • gliotoxin is part of gliotoxin biosynthetic process[9].
  • gliotoxin's Commons category is recorded as Gliotoxin[10].
  • gliotoxin's found in taxon is recorded as Aspergillus fumigatus[11].
  • gliotoxin's found in taxon is recorded as Aspergillus flavus[12].
  • gliotoxin's found in taxon is recorded as Aspergillus cejpii[13].
  • gliotoxin's found in taxon is recorded as Trichoderma deliquescens[14].
  • gliotoxin's found in taxon is recorded as Gliocladium flavofuscum[15].
  • gliotoxin's found in taxon is recorded as Trichoderma virens[16].
  • gliotoxin's found in taxon is recorded as Penicillium glabrum[17].
  • gliotoxin's found in taxon is recorded as Trichoderma viride[18].
  • gliotoxin's found in taxon is recorded as Streptomyces[19].
  • gliotoxin's found in taxon is recorded as Penicillium[20].
  • gliotoxin's found in taxon is recorded as Dichotomomyces cejpii[21].
  • gliotoxin's found in taxon is recorded as Metulocladosporiella[22].
  • gliotoxin's isomeric SMILES is recorded as CN1C(=O)[C@]23CC4=CC=CC@@HOC@@HO">[23].
  • gliotoxin's mass is recorded as {'unit': 'Q483261', 'amount': '+326.039'}[24].
  • gliotoxin's subject has role is recorded as immunosuppressive drug[25].
  • gliotoxin's stereoisomer of is recorded as (1R,7S,8R,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[26].

Why It Matters

gliotoxin has Wikipedia articles in 9 language editions, a strong signal of global cultural recognition.[2]

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [3] . wikidata.org.
  2. [4] . PubChem. Retrieved . wikidata.org.
  3. [5] . PubChem. Retrieved . wikidata.org.
  4. [6] . wikidata.org.
  5. [7] . Gene Ontology release 2019-11-16. wikidata.org.
  6. [8] . Gene Ontology release 2019-11-16. wikidata.org.
  7. [9] . Gene Ontology release 2020-05-02. wikidata.org.
  8. [10] . wikidata.org.
  9. [11] . The isolation and identification of a new metabolite from Aspergillus fumigatus related to gliotoxin. wikidata.org.
  10. [12] . An Inhibitor of Acetolactate Synthase from a Microbe. wikidata.org.
  11. [13] . Production, mutagenicity, and immunotoxicity of gliotoxin. wikidata.org.
  12. [14] . New piperazinedione metabolites of Gliocladium deliquescens. wikidata.org.
  13. [15] . Metabolites of Gliocladium flavofuscum. wikidata.org.
  14. [16] . New co-metabolites of gliotoxin in Gliocladium virens. wikidata.org.
  15. [17] . Gliotoxin-E: A New Biologically-Active Epipolythiodioxopiperazine Isolated From Penicillium terlikowskii. wikidata.org.
  16. [18] . cyclo-(L-Phenylalanyl-L-seryl) as an intermediate in the biosynthesis of gliotoxin. wikidata.org.
  17. [19] . Julichrome derivatives and gliotoxin from a soil derived Streptomyces sp. wikidata.org.
  18. [20] . Gliotoxin analogues from a marine-derived fungus, Penicillium sp., and their cytotoxic and histone methyltransferase inhibitory activities. wikidata.org.
  19. [21] . Production, mutagenicity, and immunotoxicity of gliotoxin. wikidata.org.
  20. [22] . Isolation, structure, and biological activities of Fellutamides C and D from an undescribed Metulocladosporiella (Chaetothyriales) using the genome-wide Candida albicans fitness test. wikidata.org.
  21. [23] . PubChem. Retrieved . wikidata.org.
  22. [24] . PubChem. Retrieved . wikidata.org.
  23. [25] . Medical Subject Headings. Retrieved . wikidata.org.
  24. [26] . wikidata.org.

Class ancestry

  1. [1] . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] . Wikidata sitelinks. wikidata.org.

📑 Cite this page

Use these citations when quoting this entity in research, articles, AI prompts, or wherever provenance matters. We aggregate Wikidata + Wikipedia + authoritative open-data sources; the stitched, scored, cross-referenced view is what 4ort.xyz contributes.

APA 4ort.xyz Knowledge Graph. (2026). gliotoxin. Retrieved May 3, 2026, from https://4ort.xyz/entity/gliotoxin
MLA “gliotoxin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/gliotoxin.
BibTeX @misc{4ortxyz_gliotoxin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{gliotoxin}}, year = {2026}, url = {https://4ort.xyz/entity/gliotoxin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): gliotoxin — https://4ort.xyz/entity/gliotoxin (retrieved 2026-05-03)

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Edit History

Rolling log of changes to this entity's Wikidata record. Values shown reflect the current state of each edited property — follow the history link to see the precise diff for any edit.

  1. 5w ago · Nabbegat · 2026-06-19 view diff on Wikidata ↗
    Stereoisomer of (1R,7S,8R,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
    Instance of type of chemical entity
    Part of
    Subclass of
    + 7 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update-languages-short:0||tr */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/37300|batch #37300]]"
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