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deoxynivalenol

chemical compound
ChemicalSubstance type_of_chemical_entity Q420518
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deoxynivalenol

Summary

deoxynivalenol is a type of chemical entity[1]. deoxynivalenol ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (45 views/month).[2]

Key Facts

  • deoxynivalenol's instance of is recorded as type of chemical entity[3].
  • deoxynivalenol's chemical structure is recorded as Deoxynivalenol.png[4].
  • deoxynivalenol's GND ID is recorded as 4297820-8[5].
  • deoxynivalenol's CAS Registry Number is recorded as 51481-10-8[6].
  • deoxynivalenol's EC number is recorded as 610-668-0[7].
  • deoxynivalenol's canonical SMILES is recorded as CC1=CC2C(C(C1=O)O)(C3(CC(C(C34CO4)O2)O)C)CO[8].
  • deoxynivalenol's InChI is recorded as InChI=1S/C15H20O6/c1-7-3-9-14(5-16,11(19)10(7)18)13(2)4-8(17)12(21-9)15(13)6-20-15/h3,8-9,11-12,16-17,19H,4-6H2,1-2H3/t8-,9-,11-,12-,13-,14-,15+/m1/s1[9].
  • deoxynivalenol's InChIKey is recorded as LINOMUASTDIRTM-QGRHZQQGSA-N[10].
  • deoxynivalenol's chemical formula is recorded as C₁₅H₂₀O₆[11].
  • deoxynivalenol's subclass of is recorded as Rd toxin[12].
  • deoxynivalenol's part of is recorded as vomitoxin biosynthetic process[13].
  • deoxynivalenol's Commons category is recorded as Vomitoxin[14].
  • deoxynivalenol's MeSH descriptor ID is recorded as C007262[15].
  • deoxynivalenol's ChEMBL ID is recorded as CHEMBL513300[16].
  • deoxynivalenol's Freebase ID is recorded as /m/02z48jh[17].
  • deoxynivalenol's UNII is recorded as JT37HYP23V[18].
  • deoxynivalenol's ChemSpider ID is recorded as 36584[19].
  • deoxynivalenol's PubChem CID is recorded as 40024[20].
  • deoxynivalenol's KEGG ID is recorded as C09747[21].
  • deoxynivalenol's ChEBI ID is recorded as 10022[22].
  • deoxynivalenol's found in taxon is recorded as Fusarium roseum[23].
  • deoxynivalenol's found in taxon is recorded as Fusarium culmorum[24].
  • deoxynivalenol's found in taxon is recorded as Fusarium graminearum[25].
  • deoxynivalenol's NALT ID is recorded as 32387[26].
  • deoxynivalenol's isomeric SMILES is recorded as CC1=C[C@@H]2C@([C@]3(CC@HO)C)COC@([C@]3(CC@HO)C)CO">[27].

Why It Matters

deoxynivalenol ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (45 views/month).[2] deoxynivalenol has Wikipedia articles in 13 language editions, a strong signal of global cultural recognition.[28] deoxynivalenol is known by 16 alternative names across languages and contexts.[29]

References

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

Direct Wikidata claims

  1. [3] ↑ . wikidata.org.
  2. [4] ↑ . wikidata.org.
  3. [5] ↑ . wikidata.org.
  4. [6] ↑ . Global Substance Registration System. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  5. [7] ↑ . ECHA Substance Infocard database. Retrieved . wikidata.org.
  6. [8] ↑ . PubChem. Retrieved . wikidata.org.
  7. [9] ↑ . PubChem. Retrieved . wikidata.org.
  8. [10] ↑ . PubChem. Retrieved . wikidata.org.
  9. [11] ↑ . PubChem. Retrieved . wikidata.org.
  10. [12] ↑ . wikidata.org.
  11. [13] ↑ . Gene Ontology release 2022-07-01. wikidata.org.
  12. [14] ↑ . wikidata.org.
  13. [15] ↑ . wikidata.org.
  14. [16] ↑ . ChEMBL. Retrieved . wikidata.org.
  15. [17] ↑ . Freebase Data Dumps. wikidata.org.
  16. [18] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  17. [19] ↑ . Q2311683. Retrieved . wikidata.org.
  18. [20] ↑ . PubChem. Retrieved . wikidata.org.
  19. [21] ↑ . wikidata.org.
  20. [22] ↑ . ChEBI release 2019-10-02. wikidata.org.
  21. [23] ↑ . Microbial Correlates of Fusarium Load and Deoxynivalenol Content in Individual Wheat Kernels. wikidata.org.
  22. [24] ↑ . Occurrence of Gibberella zeae strains that produce both nivalenol and deoxynivalenol. wikidata.org.
  23. [25] ↑ . Acetylated mycotoxins from Fusarium graminearum. wikidata.org.
  24. [26] ↑ . wikidata.org.
  25. [27] ↑ . PubChem. Retrieved . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . Wikimedia Foundation. dumps.wikimedia.org.
  2. [28] ↑ . Wikidata sitelinks. wikidata.org.
  3. [29] ↑ . Wikidata aliases. 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). deoxynivalenol. Retrieved May 3, 2026, from https://4ort.xyz/entity/deoxynivalenol
MLA “deoxynivalenol.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/deoxynivalenol.
BibTeX @misc{4ortxyz_deoxynivalenol_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{deoxynivalenol}}, year = {2026}, url = {https://4ort.xyz/entity/deoxynivalenol}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): deoxynivalenol — https://4ort.xyz/entity/deoxynivalenol (retrieved 2026-05-03)

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