dipyridamole

medication that inhibits blood clot formation[3] when given chronically and causes blood vessel dilation when given at high doses over a short time
ChemicalSubstance type_of_chemical_entity Q419374
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dipyridamole

Summary

dipyridamole is a type of chemical entity[1]. dipyridamole ranks in the top 5% of type_of_chemical_entity entities by monthly Wikipedia readership (63 views/month).[2]

Key Facts

  • dipyridamole's instance of is recorded as type of chemical entity[3].
  • dipyridamole's physically interacts with is recorded as Solute carrier family 29 member 1 (Augustine blood group)[4].
  • dipyridamole's physically interacts with is recorded as Phosphodiesterase 7B[5].
  • dipyridamole's physically interacts with is recorded as Phosphodiesterase 8A[6].
  • dipyridamole's physically interacts with is recorded as Phosphodiesterase 8B[7].
  • dipyridamole's physically interacts with is recorded as Solute carrier family 29 member 4[8].
  • dipyridamole's canonical SMILES is recorded as C1CCN(CC1)C2=NC(=NC3=C2N=C(N=C3N4CCCCC4)N(CCO)CCO)N(CCO)CCO[9].
  • dipyridamole's chemical formula is recorded as C₂₄H₄₀N₈O₄[10].
  • dipyridamole is a type of piperidine alkaloids[11].
  • dipyridamole is used for medication[12].
  • dipyridamole's Commons category is recorded as Dipyridamole[13].
  • dipyridamole's found in taxon is recorded as Heracleum candicans[14].
  • dipyridamole's found in taxon is recorded as Prangos ferulacea[15].
  • dipyridamole's has characteristic is recorded as bitterness[16].
  • dipyridamole's mass is recorded as {'unit': 'Q483261', 'amount': '+504.317252'}[17].
  • dipyridamole's World Health Organisation international non-proprietary name is recorded as {'lang': 'en', 'text': 'dipyridamole'}[18].
  • dipyridamole's studied by is recorded as emergency medicine[19].
  • dipyridamole's subject has role is recorded as phosphodiesterase inhibitor[20].
  • dipyridamole's subject has role is recorded as vasodilator agent[21].
  • dipyridamole's subject has role is recorded as platelet aggregation inhibitors[22].
  • dipyridamole's active ingredient in is recorded as Persantine[23].
  • dipyridamole's has active ingredient is recorded as Dipyridamole[24].

Why It Matters

dipyridamole ranks in the top 5% of type_of_chemical_entity entities by monthly Wikipedia readership (63 views/month).[2] dipyridamole has Wikipedia articles in 19 language editions, a strong signal of global cultural recognition.[25] dipyridamole is known by 16 alternative names across languages and contexts.[26]

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] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  5. [7] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  6. [8] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  7. [9] . PubChem. Retrieved . wikidata.org.
  8. [10] . PubChem. Retrieved . wikidata.org.
  9. [11] . wikidata.org.
  10. [12] . wikidata.org.
  11. [13] . wikidata.org.
  12. [14] . Chemical studies on the root of Heracleum candicans Wall. wikidata.org.
  13. [15] . Isogosferol — A new furocoumarin from the roots of Prangos lophoptera. wikidata.org.
  14. [16] . BitterDB. wikidata.org.
  15. [17] . PubChem. Retrieved . wikidata.org.
  16. [18] . ChEBI. Retrieved . wikidata.org.
  17. [19] . wikidata.org.
  18. [20] . NDF-RT. Retrieved . wikidata.org.
  19. [21] . Medical Subject Headings. Retrieved . wikidata.org.
  20. [22] . Medical Subject Headings. Retrieved . wikidata.org.
  21. [23] . RxNorm. Retrieved . wikidata.org.
  22. [24] . wikidata.org.

Class ancestry

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

Aggregate / graph-position facts

  1. [2] . Wikimedia Foundation. dumps.wikimedia.org.
  2. [25] . Wikidata sitelinks. wikidata.org.
  3. [26] . 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). dipyridamole. Retrieved May 3, 2026, from https://4ort.xyz/entity/dipyridamole
MLA “dipyridamole.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/dipyridamole.
BibTeX @misc{4ortxyz_dipyridamole_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{dipyridamole}}, year = {2026}, url = {https://4ort.xyz/entity/dipyridamole}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): dipyridamole — https://4ort.xyz/entity/dipyridamole (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/dipyridamole · 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. 21d ago · FlocciNivis · 2026-06-25 view diff on Wikidata ↗
    Aliases
    Subclass of piperidine alkaloids
    Mass {'unit': 'Q483261', 'amount': '+504.317252'}
    Instance of
    + 11 other properties edited (see Wikidata diff for full list)
    "/* wbcreateclaim-create:1| */ [[Property:P3636]]: H9F, [[:toollabs:quickstatements/#/batch/259826|batch #259826]]"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.