vidarabine

chemical compound
ChemicalSubstance type_of_chemical_entity Q415107
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vidarabine

Summary

vidarabine is a type of chemical entity[1]. vidarabine ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (55 views/month).[2]

Key Facts

  • vidarabine's instance of is recorded as type of chemical entity[3].
  • vidarabine's canonical SMILES is recorded as C1=NC2=C(C(=N1)N)N=CN2C3C(C(C(O3)CO)O)O[4].
  • vidarabine's chemical formula is recorded as C₁₀H₁₃N₅O₄[5].
  • vidarabine is a type of 2-(6-Aminopurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol[6].
  • vidarabine is used for medication[7].
  • vidarabine's Commons category is recorded as Vidarabine[8].
  • vidarabine's found in taxon is recorded as Tillandsia usneoides[9].
  • vidarabine's found in taxon is recorded as Daucus carota[10].
  • vidarabine's found in taxon is recorded as Eunicella cavolini[11].
  • vidarabine's found in taxon is recorded as Streptomyces antibioticus[12].
  • vidarabine's found in taxon is recorded as Streptomyces herbaceus[13].
  • vidarabine's catalog is recorded as CAS COVID-19 Anti-Viral Candidate Compounds[14].
  • vidarabine's isomeric SMILES is recorded as C1=NC2=C(C(=N1)N)N=CN2[C@H]3C@HOC@HO">[15].
  • vidarabine's mass is recorded as {'unit': 'Q483261', 'amount': '+267.097'}[16].
  • vidarabine's medical condition treated is recorded as herpes simplex[17].
  • vidarabine's medical condition treated is recorded as herpes simplex virus keratitis[18].
  • vidarabine's subject has role is recorded as DNA polymerase inhibitors[19].
  • vidarabine's subject has role is recorded as antiviral agent[20].
  • vidarabine's subject has role is recorded as antimetabolite[21].
  • vidarabine's stereoisomer of is recorded as 9-Beta-D-Xylofuranosyl-Adenine[22].
  • vidarabine's stereoisomer of is recorded as 9-alpha-Ribofuranosyladenine[23].
  • vidarabine's stereoisomer of is recorded as adenosine[24].
  • vidarabine's stereoisomer of is recorded as 9-beta-d-Arabinofuranosylade-nine[25].
  • vidarabine's stereoisomer of is recorded as 9-beta-D-xylofuranosyladenine[26].
  • vidarabine's stereoisomer of is recorded as Adenosine, homopolymer[27].

Why It Matters

vidarabine ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (55 views/month).[2] vidarabine has Wikipedia articles in 11 language editions, a strong signal of global cultural recognition.[28] vidarabine is known by 11 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] . PubChem. Retrieved . wikidata.org.
  3. [5] . PubChem. Retrieved . wikidata.org.
  4. [6] . wikidata.org.
  5. [7] . wikidata.org.
  6. [8] . wikidata.org.
  7. [9] . Identification of 3-Hydroxy-3-methylglutaric Acid (HMG) as a Hypoglycemic Principle of Spanish Moss (Tillandsia usneoides). wikidata.org.
  8. [10] . Structural features of cell-wall polysaccharides of the carrot Daucus carota. wikidata.org.
  9. [11] . Antiviral agents from a gorgonian,Eunicella cavolini. wikidata.org.
  10. [12] . Improved production of pentostatin and identification of fermentation cometabolites. wikidata.org.
  11. [13] . Production of 9-.BETA.-D-arabinofuranosyladenine by a new species of Streptomyces and its herbicidal activity. wikidata.org.
  12. [14] . wikidata.org.
  13. [15] . PubChem. Retrieved . wikidata.org.
  14. [16] . PubChem. Retrieved . wikidata.org.
  15. [17] . NDF-RT. Retrieved . wikidata.org.
  16. [18] . NDF-RT. Retrieved . wikidata.org.
  17. [19] . NDF-RT. Retrieved . wikidata.org.
  18. [20] . Medical Subject Headings. Retrieved . wikidata.org.
  19. [21] . Medical Subject Headings. Retrieved . wikidata.org.
  20. [22] . wikidata.org.
  21. [23] . wikidata.org.
  22. [24] . wikidata.org.
  23. [25] . wikidata.org.
  24. [26] . wikidata.org.
  25. [27] . 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). vidarabine. Retrieved May 3, 2026, from https://4ort.xyz/entity/vidarabine
MLA “vidarabine.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/vidarabine.
BibTeX @misc{4ortxyz_vidarabine_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{vidarabine}}, year = {2026}, url = {https://4ort.xyz/entity/vidarabine}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): vidarabine — https://4ort.xyz/entity/vidarabine (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/vidarabine · Last refreshed:

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. 8d ago · Twofivesixbot bot · 2026-05-25 view diff on Wikidata ↗
    Has use medication
    Instance of
    Subclass of 2-(6-Aminopurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol
    Subject has role DNA polymerase inhibitors, antiviral agent, antimetabolite
    + 8 other properties edited (see Wikidata diff for full list)
    "/* wbsetclaim-update-qualifiers:1||1|1 */ [[Property:P8189]]: 987007403823905171, mv to monolingual text names on J9U statements"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.