cidofovir

chemical compound
ChemicalSubstance type_of_chemical_entity Q423445
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cidofovir

Summary

cidofovir is a type of chemical entity[1]. cidofovir has Wikipedia articles in 16 language editions, a strong signal of global cultural recognition.[2]

Key Facts

  • cidofovir is credited with the discovery of Antonín Holý[3].
  • cidofovir's instance of is recorded as type of chemical entity[4].
  • cidofovir's canonical SMILES is recorded as C1=CN(C(=O)N=C1N)CC(CO)OCP(=O)(O)O[5].
  • cidofovir's chemical formula is recorded as C₈H₁₄N₃O₆P[6].
  • cidofovir is a type of 1-(3-Hydroxy-2-phosphonomethoxypropyl)-4-aminopyrimidin-2(1H)-one[7].
  • cidofovir is used for medication[8].
  • cidofovir's Commons category is recorded as Cidofovir[9].
  • cidofovir's catalog is recorded as CAS COVID-19 Anti-Viral Candidate Compounds[10].
  • cidofovir's isomeric SMILES is recorded as C1=CN(C(=O)N=C1N)CC@@HOCP(=O)(O)OC@@HOCP(=O)(O)O">[11].
  • cidofovir's mass is recorded as {'unit': 'Q483261', 'amount': '+279.062'}[12].
  • cidofovir's medical condition treated is recorded as cytomegaloviral disease[13].
  • cidofovir's medical condition treated is recorded as cytomegalovirus retinitis[14].
  • cidofovir's subject has role is recorded as carcinogen[15].
  • cidofovir's subject has role is recorded as developmental toxicant[16].
  • cidofovir's subject has role is recorded as male reproductive toxicant[17].
  • cidofovir's subject has role is recorded as female reproductive toxicant[18].
  • cidofovir's subject has role is recorded as antiviral drug[19].
  • cidofovir's subject has role is recorded as bactericide[20].
  • cidofovir's stereoisomer of is recorded as [(2R)-1-(4-amino-2-oxo-pyrimidin-1-yl)-3-hydroxy-propan-2-yl]oxymethylphosphonic acid[21].
  • cidofovir's pregnancy category is recorded as Australian pregnancy category D[22].
  • cidofovir's pregnancy category is recorded as US pregnancy category C[23].
  • cidofovir's legal status is recorded as boxed warning[24].
  • cidofovir's active ingredient in is recorded as Vistide[25].
  • cidofovir's has active ingredient is recorded as Cidofovir[26].
  • cidofovir's defined daily dose is recorded as {'unit': 'Q3241121', 'amount': '+25'}[27].

Body

Works and Contributions

cidofovir is credited with the discovery of Antonín Holý[3].

Why It Matters

cidofovir has Wikipedia articles in 16 language editions, a strong signal of global cultural recognition.[2] cidofovir is known by 21 alternative names across languages and contexts.[28]

References

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

Direct Wikidata claims

  1. [4] . wikidata.org.
  2. [3] . wikidata.org.
  3. [5] . PubChem. Retrieved . wikidata.org.
  4. [6] . PubChem. Retrieved . wikidata.org.
  5. [7] . wikidata.org.
  6. [8] . DrugBank. wikidata.org.
  7. [9] . wikidata.org.
  8. [10] . wikidata.org.
  9. [11] . PubChem. Retrieved . wikidata.org.
  10. [12] . PubChem. Retrieved . wikidata.org.
  11. [13] . NDF-RT. Retrieved . wikidata.org.
  12. [14] . NDF-RT. Retrieved . wikidata.org.
  13. [15] . California Proposition 65 list of chemicals. Retrieved . oehha.ca.gov. Provenance: wikidata.org.
  14. [16] . California Proposition 65 list of chemicals. Retrieved . oehha.ca.gov. Provenance: wikidata.org.
  15. [17] . California Proposition 65 list of chemicals. Retrieved . oehha.ca.gov. Provenance: wikidata.org.
  16. [18] . California Proposition 65 list of chemicals. Retrieved . oehha.ca.gov. Provenance: wikidata.org.
  17. [19] . ChEBI. wikidata.org.
  18. [20] . ChEBI. wikidata.org.
  19. [21] . wikidata.org.
  20. [22] . wikidata.org.
  21. [23] . wikidata.org.
  22. [24] . nctr-crs.fda.gov. nctr-crs.fda.gov. Provenance: wikidata.org.
  23. [25] . ema.europa.eu. Retrieved . ema.europa.eu. Provenance: wikidata.org.
  24. [26] . wikidata.org.
  25. [27] . whocc.no. whocc.no. Provenance: wikidata.org.

Class ancestry

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

Aggregate / graph-position facts

  1. [2] . Wikidata sitelinks. wikidata.org.
  2. [28] . 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). cidofovir. Retrieved May 3, 2026, from https://4ort.xyz/entity/cidofovir
MLA “cidofovir.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/cidofovir.
BibTeX @misc{4ortxyz_cidofovir_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{cidofovir}}, year = {2026}, url = {https://4ort.xyz/entity/cidofovir}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): cidofovir — https://4ort.xyz/entity/cidofovir (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. 28d ago · Nabbegat · 2026-06-19 view diff on Wikidata ↗
    Defined daily dose {'unit': 'Q3241121', 'amount': '+25'}
    Legal status (medicine) boxed warning
    Stereoisomer of [(2R)-1-(4-amino-2-oxo-pyrimidin-1-yl)-3-hydroxy-propan-2-yl]oxymethylphosphonic acid
    Instance of type of chemical entity
    + 13 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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