vinpocetine

chemical compound
ChemicalSubstance type_of_chemical_entity Q420288
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vinpocetine

Summary

vinpocetine is a type of chemical entity[1]. vinpocetine ranks in the top 5% of type_of_chemical_entity entities by monthly Wikipedia readership (100 views/month).[2]

Key Facts

  • vinpocetine's instance of is recorded as type of chemical entity[3].
  • vinpocetine's chemical structure is recorded as Vinpocetin.svg[4].
  • vinpocetine's chemical structure is recorded as Vinpocetine.svg[5].
  • vinpocetine's CAS Registry Number is recorded as 42971-09-5[6].
  • vinpocetine's EC number is recorded as 256-028-0[7].
  • vinpocetine's canonical SMILES is recorded as CCC12CCCN3C1C4=C(CC3)C5=CC=CC=C5N4C(=C2)C(=O)OCC[8].
  • vinpocetine's InChI is recorded as InChI=1S/C22H26N2O2/c1-3-22-11-7-12-23-13-10-16-15-8-5-6-9-17(15)24(19(16)20(22)23)18(14-22)21(25)26-4-2/h5-6,8-9,14,20H,3-4,7,10-13H2,1-2H3/t20-,22+/m1/s1[9].
  • vinpocetine's InChIKey is recorded as DDNCQMVWWZOMLN-IRLDBZIGSA-N[10].
  • vinpocetine's ATC code is recorded as N06BX18[11].
  • vinpocetine's chemical formula is recorded as C₂₂H₂₆N₂O₂[12].
  • vinpocetine's subclass of is recorded as LSM-1372[13].
  • vinpocetine's has use is recorded as medication[14].
  • vinpocetine's Commons category is recorded as Vinpocetine[15].
  • vinpocetine's MeSH descriptor ID is recorded as C013983[16].
  • vinpocetine's ChEMBL ID is recorded as CHEMBL71752[17].
  • vinpocetine's Guide to Pharmacology Ligand ID is recorded as 5285[18].
  • vinpocetine's route of administration is recorded as oral administration[19].
  • vinpocetine's route of administration is recorded as intravenous infusion and defusionههبهلخل[20].
  • vinpocetine's Freebase ID is recorded as /m/0bxf8t[21].
  • vinpocetine's UNII is recorded as 543512OBTC[22].
  • vinpocetine's ChemSpider ID is recorded as 392007[23].
  • vinpocetine's PubChem CID is recorded as 443955[24].
  • vinpocetine's ChEBI ID is recorded as 32297[25].
  • vinpocetine's DrugBank ID is recorded as DB12131[26].
  • vinpocetine's isomeric SMILES is recorded as CC[C@@]12CCCN3[C@@H]1C4=C(CC3)C5=CC=CC=C5N4C(=C2)C(=O)OCC[27].

Why It Matters

vinpocetine ranks in the top 5% of type_of_chemical_entity entities by monthly Wikipedia readership (100 views/month).[2] vinpocetine has Wikipedia articles in 11 language editions, a strong signal of global cultural recognition.[28] vinpocetine is known by 19 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] . wikidata.org.
  3. [5] . wikidata.org.
  4. [6] . Global Substance Registration System. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  5. [7] . Global Substance Registration System. Retrieved . wikidata.org.
  6. [8] . PubChem. Retrieved . wikidata.org.
  7. [9] . PubChem. Retrieved . wikidata.org.
  8. [10] . PubChem. Retrieved . wikidata.org.
  9. [11] . wikidata.org.
  10. [12] . PubChem. Retrieved . wikidata.org.
  11. [13] . wikidata.org.
  12. [14] . wikidata.org.
  13. [15] . wikidata.org.
  14. [16] . Medical Subject Headings. Retrieved . wikidata.org.
  15. [17] . ChEMBL. Retrieved . wikidata.org.
  16. [18] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  17. [19] . wikidata.org.
  18. [20] . wikidata.org.
  19. [21] . Freebase Data Dumps. wikidata.org.
  20. [22] . Global Substance Registration System. Retrieved . wikidata.org.
  21. [23] . Q2311683. Retrieved . wikidata.org.
  22. [24] . PubChem. Retrieved . wikidata.org.
  23. [25] . ChEBI release 2019-10-02. wikidata.org.
  24. [26] . wikidata.org.
  25. [27] . PubChem. Retrieved . 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). vinpocetine. Retrieved May 3, 2026, from https://4ort.xyz/entity/vinpocetine
MLA “vinpocetine.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/vinpocetine.
BibTeX @misc{4ortxyz_vinpocetine_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{vinpocetine}}, year = {2026}, url = {https://4ort.xyz/entity/vinpocetine}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): vinpocetine — https://4ort.xyz/entity/vinpocetine (retrieved 2026-05-03)

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