5-hydroxyisouric acid

chemical compound
ChemicalSubstance type_of_chemical_entity Q2823232
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5-hydroxyisouric acid

Summary

5-hydroxyisouric acid is a type of chemical entity[1]. It ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (5 views/month).[2]

Key Facts

  • 5-hydroxyisouric acid's instance of is recorded as type of chemical entity[3].
  • 5-hydroxyisouric acid's CAS Registry Number is recorded as 6960-30-1[4].
  • 5-hydroxyisouric acid's canonical SMILES is recorded as C12=NC(=O)NC1(C(=O)NC(=O)N2)O[5].
  • 5-hydroxyisouric acid's InChI is recorded as InChI=1S/C5H4N4O4/c10-2-5(13)1(6-3(11)8-2)7-4(12)9-5/h13H,(H3,6,7,8,9,10,11,12)[6].
  • 5-hydroxyisouric acid's InChIKey is recorded as LTQYPAVLAYVKTK-UHFFFAOYSA-N[7].
  • 5-hydroxyisouric acid's chemical formula is recorded as C₅H₄N₄O₄[8].
  • 5-hydroxyisouric acid's subclass of is recorded as purine alkaloid[9].
  • 5-hydroxyisouric acid's part of is recorded as urate oxidase activity[10].
  • 5-hydroxyisouric acid's part of is recorded as hydroxyisourate hydrolase activity[11].
  • 5-hydroxyisouric acid's part of is recorded as FAD-dependent urate hydroxylase activity[12].
  • 5-hydroxyisouric acid's Freebase ID is recorded as /m/0gclrd[13].
  • 5-hydroxyisouric acid's UNII is recorded as DU6PJ7L9BX[14].
  • 5-hydroxyisouric acid's ChemSpider ID is recorded as 219288[15].
  • 5-hydroxyisouric acid's ChemSpider ID is recorded as 21233342[16].
  • 5-hydroxyisouric acid's PubChem CID is recorded as 250388[17].
  • 5-hydroxyisouric acid's KEGG ID is recorded as C11821[18].
  • 5-hydroxyisouric acid's ChEBI ID is recorded as 18072[19].
  • 5-hydroxyisouric acid's found in taxon is recorded as Homo sapiens[20].
  • 5-hydroxyisouric acid's found in taxon is recorded as Caenorhabditis elegans[21].
  • 5-hydroxyisouric acid's Reaxys registry number is recorded as 5949568[22].
  • 5-hydroxyisouric acid's KNApSAcK ID is recorded as C00007531[23].
  • 5-hydroxyisouric acid's KNApSAcK ID is recorded as C00062716[24].
  • 5-hydroxyisouric acid's mass is recorded as {'unit': 'Q483261', 'amount': '+184.023255'}[25].
  • 5-hydroxyisouric acid's NSC number is recorded as 69826[26].
  • 5-hydroxyisouric acid's subject has role is recorded as primary metabolite[27].

Why It Matters

5-hydroxyisouric acid ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (5 views/month).[2] It has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[28] It is known by 3 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] . ChEBI. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  3. [5] . PubChem. Retrieved . wikidata.org.
  4. [6] . PubChem. Retrieved . wikidata.org.
  5. [7] . PubChem. Retrieved . wikidata.org.
  6. [8] . PubChem. Retrieved . wikidata.org.
  7. [9] . wikidata.org.
  8. [10] . Gene Ontology release 2020-05-02. wikidata.org.
  9. [11] . Gene Ontology release 2020-05-02. wikidata.org.
  10. [12] . Gene Ontology release 2020-05-02. wikidata.org.
  11. [13] . Freebase Data Dumps. wikidata.org.
  12. [14] . wikidata.org.
  13. [15] . Q2311683. Retrieved . wikidata.org.
  14. [16] . Q2311683. Retrieved . wikidata.org.
  15. [17] . PubChem. Retrieved . wikidata.org.
  16. [18] . wikidata.org.
  17. [19] . ChEBI. Retrieved . wikidata.org.
  18. [20] . Recon 2.2: from reconstruction to model of human metabolism. wikidata.org.
  19. [21] . Modeling Meets Metabolomics-The WormJam Consensus Model as Basis for Metabolic Studies in the Model Organism. wikidata.org.
  20. [22] . ChEBI. Retrieved . wikidata.org.
  21. [23] . ChEBI. Retrieved . wikidata.org.
  22. [24] . wikidata.org.
  23. [25] . PubChem. Retrieved . wikidata.org.
  24. [26] . wikidata.org.
  25. [27] . Reactome. plantreactome.gramene.org. Provenance: 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). 5-hydroxyisouric acid. Retrieved May 3, 2026, from https://4ort.xyz/entity/5-hydroxyisouric-acid
MLA “5-hydroxyisouric acid.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/5-hydroxyisouric-acid.
BibTeX @misc{4ortxyz_5-hydroxyisouric-acid_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{5-hydroxyisouric acid}}, year = {2026}, url = {https://4ort.xyz/entity/5-hydroxyisouric-acid}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): 5-hydroxyisouric acid — https://4ort.xyz/entity/5-hydroxyisouric-acid (retrieved 2026-05-03)

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