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prostaglandin D2

chemical compound
ChemicalSubstance type_of_chemical_entity Q419750
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prostaglandin D2

Summary

prostaglandin D2 is a type of chemical entity[1]. It has Wikipedia articles in 8 language editions, a strong signal of global cultural recognition.[2]

Key Facts

  • prostaglandin D2's instance of is recorded as type of chemical entity[3].
  • prostaglandin D2's physically interacts with is recorded as Prostaglandin D2 receptor[4].
  • prostaglandin D2's physically interacts with is recorded as Prostaglandin D2 receptor 2[5].
  • prostaglandin D2's canonical SMILES is recorded as CCCCCC(C=CC1C(C(CC1=O)O)CC=CCCCC(=O)O)O[6].
  • prostaglandin D2's chemical formula is recorded as C₂₀H₃₂O₅[7].
  • prostaglandin D2 is a type of prostaglandins[8].
  • prostaglandin D2's Commons category is recorded as Prostaglandin D2[9].
  • prostaglandin D2's found in taxon is recorded as Gersemia fruticosa[10].
  • prostaglandin D2's found in taxon is recorded as Larix sibirica[11].
  • prostaglandin D2's found in taxon is recorded as Homo sapiens[12].
  • prostaglandin D2's isomeric SMILES is recorded as CCCCCC@@HOC@@HO">[13].
  • prostaglandin D2's mass is recorded as {'unit': 'Q483261', 'amount': '+352.225'}[14].
  • prostaglandin D2's subject has role is recorded as primary metabolite[15].
  • prostaglandin D2's stereoisomer of is recorded as 7-[(1R,2R,5S)-5-hydroxy-2-[(1E,3S)-3-hydroxyoct-1-en-1-yl]-3-oxocyclopentyl]hept-5-enoic acid[16].
  • prostaglandin D2's stereoisomer of is recorded as 9S,15S-dihydroxy-11-oxo-5Z,13E-prostadienoic acid-cyclo[8R,12S][17].
  • prostaglandin D2's stereoisomer of is recorded as 11-oxo-9R,15S-dihydroxy-5Z,13E-prostadienoic acid-cyclo[8R,12R][18].
  • prostaglandin D2's stereoisomer of is recorded as 9S,15R-dihydroxy-11-oxo-5Z,13E-prostadienoic acid-cyclo[8R,12S][19].
  • prostaglandin D2's stereoisomer of is recorded as 11-oxo-9S,15R-dihydroxy-5Z,13E-prostadienoic acid-cyclo[8S,12S][20].
  • prostaglandin D2's stereoisomer of is recorded as LSM-5269[21].
  • prostaglandin D2's stereoisomer of is recorded as 9R,15S-dihydroxy-11-oxo-5Z,13E-prostadienoic acid-cyclo[8R,12S][22].
  • prostaglandin D2's stereoisomer of is recorded as (Z)-7-[(1S,2R,5S)-5-hydroxy-2-[(E,3S)-3-hydroxyoct-1-enyl]-3-oxocyclopentyl]hept-5-enoic acid[23].
  • prostaglandin D2's stereoisomer of is recorded as (Z)-7-[(1R,2S,5R)-5-hydroxy-2-[(E,3R)-3-hydroxyoct-1-enyl]-3-oxocyclopentyl]hept-5-enoic acid[24].
  • prostaglandin D2's stereoisomer of is recorded as 5-trans Prostaglandin D2[25].
  • prostaglandin D2's stereoisomer of is recorded as (Z)-7-[(1R,2R,5R)-5-hydroxy-2-[(E,3R)-3-hydroxyoct-1-enyl]-3-oxocyclopentyl]hept-5-enoic acid[26].
  • prostaglandin D2's stereoisomer of is recorded as 9R,15R-dihydroxy-11-oxo-5Z,13E-prostadienoic acid-cyclo[8S,12R][27].

Why It Matters

prostaglandin D2 has Wikipedia articles in 8 language editions, a strong signal of global cultural recognition.[2] It is known by 32 alternative names across languages and contexts.[28]

References

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

Direct Wikidata claims

  1. [3] ↑ . wikidata.org.
  2. [4] ↑ . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  3. [5] ↑ . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  4. [6] ↑ . PubChem. Retrieved . wikidata.org.
  5. [7] ↑ . PubChem. Retrieved . wikidata.org.
  6. [8] ↑ . wikidata.org.
  7. [9] ↑ . wikidata.org.
  8. [10] ↑ . In vitro biosynthesis of prostaglandins in the White Sea soft coral Gersemia fruticosa: Formation of optically active PGD2, PGE2, PGF2α and 15-keto-PGF2α from arachidonic acid. wikidata.org.
  9. [11] ↑ . Detection of prostaglandin F2? in tissues of Populus balsamifera and Larix sibirica. wikidata.org.
  10. [12] ↑ . Recon 2.2: from reconstruction to model of human metabolism. wikidata.org.
  11. [13] ↑ . PubChem. Retrieved . wikidata.org.
  12. [14] ↑ . PubChem. Retrieved . wikidata.org.
  13. [15] ↑ . Reactome. reactome.org. Provenance: wikidata.org.
  14. [16] ↑ . wikidata.org.
  15. [17] ↑ . wikidata.org.
  16. [18] ↑ . wikidata.org.
  17. [19] ↑ . wikidata.org.
  18. [20] ↑ . wikidata.org.
  19. [21] ↑ . 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] ↑ . Wikidata sitelinks. wikidata.org.
  2. [28] ↑ . Wikidata aliases. wikidata.org.

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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). prostaglandin D2. Retrieved May 3, 2026, from https://4ort.xyz/entity/prostaglandin-d2
MLA “prostaglandin D2.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/prostaglandin-d2.
BibTeX @misc{4ortxyz_prostaglandin-d2_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{prostaglandin D2}}, year = {2026}, url = {https://4ort.xyz/entity/prostaglandin-d2}, note = {Accessed: 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 → 7-[(1R,2R,5S)-5-hydroxy-2-[(1E,3S)-3-hydroxyoct-1-en-1-yl]-3-oxocyclopentyl]hept-5-enoic acid, 9S,15S-dihydroxy-11-oxo-5Z,13E-prostadienoic acid-cyclo[8R,12S], 11-oxo-9R,15S-dihydroxy-5Z,13E-prostadienoic acid-cyclo[8R,12R] +15
    Instance of → type of chemical entity
    Subclass of → —
    Aliases → —
    + 6 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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