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(2R,3S,4S)-leucocyanidin

chemical compound
ChemicalSubstance type_of_chemical_entity Q8085718
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(2R,3S,4S)-leucocyanidin

Summary

(2R,3S,4S)-leucocyanidin is a type of chemical entity[1]. (2R,3S,4S)-leucocyanidin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (11 views/month).[2]

Key Facts

  • (2R,3S,4S)-leucocyanidin's instance of is recorded as type of chemical entity[3].
  • (2R,3S,4S)-leucocyanidin's chemical structure is recorded as Leucocyanidin.svg[4].
  • (2R,3S,4S)-leucocyanidin's CAS Registry Number is recorded as 93527-39-0[5].
  • (2R,3S,4S)-leucocyanidin's canonical SMILES is recorded as C1=CC(=C(C=C1C2C(C(C3=C(C=C(C=C3O2)O)O)O)O)O)O[6].
  • (2R,3S,4S)-leucocyanidin's InChI is recorded as InChI=1S/C15H14O7/c16-7-4-10(19)12-11(5-7)22-15(14(21)13(12)20)6-1-2-8(17)9(18)3-6/h1-5,13-21H/t13-,14-,15+/m0/s1[7].
  • (2R,3S,4S)-leucocyanidin's InChIKey is recorded as SBZWTSHAFILOTE-SOUVJXGZSA-N[8].
  • (2R,3S,4S)-leucocyanidin's chemical formula is recorded as C₁₅H₁₄O₇[9].
  • (2R,3S,4S)-leucocyanidin's subclass of is recorded as leucocyanidin (unspec. stereochem.)[10].
  • (2R,3S,4S)-leucocyanidin's part of is recorded as leucoanthocyanidin reductase activity[11].
  • (2R,3S,4S)-leucocyanidin's Commons category is recorded as Leucocyanidin[12].
  • (2R,3S,4S)-leucocyanidin's ChEMBL ID is recorded as CHEMBL124022[13].
  • (2R,3S,4S)-leucocyanidin's Freebase ID is recorded as /m/07k9lql[14].
  • (2R,3S,4S)-leucocyanidin's ChemSpider ID is recorded as 389677[15].
  • (2R,3S,4S)-leucocyanidin's PubChem CID is recorded as 440833[16].
  • (2R,3S,4S)-leucocyanidin's KEGG ID is recorded as C05906[17].
  • (2R,3S,4S)-leucocyanidin's KEGG ID is recorded as D08112[18].
  • (2R,3S,4S)-leucocyanidin's ChEBI ID is recorded as 11412[19].
  • (2R,3S,4S)-leucocyanidin's found in taxon is recorded as Terminalia arjuna[20].
  • (2R,3S,4S)-leucocyanidin's found in taxon is recorded as Arabidopsis thaliana[21].
  • (2R,3S,4S)-leucocyanidin's found in taxon is recorded as Cassia javanica[22].
  • (2R,3S,4S)-leucocyanidin's found in taxon is recorded as Gossypium hirsutum[23].
  • (2R,3S,4S)-leucocyanidin's found in taxon is recorded as Koenigia coriaria[24].
  • (2R,3S,4S)-leucocyanidin's found in taxon is recorded as Matthiola incana[25].
  • (2R,3S,4S)-leucocyanidin's Reaxys registry number is recorded as 6574536[26].
  • (2R,3S,4S)-leucocyanidin's isomeric SMILES is recorded as C1=CC(=C(C=C1[C@@H]2C@HO)O)OC@HO)O)O">[27].

Why It Matters

(2R,3S,4S)-leucocyanidin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (11 views/month).[2] (2R,3S,4S)-leucocyanidin has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[28] (2R,3S,4S)-leucocyanidin is known by 11 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] ↑ . ChemIDplus. Retrieved . chem.sis.nlm.nih.gov. Provenance: wikidata.org.
  4. [6] ↑ . PubChem. Retrieved . wikidata.org.
  5. [7] ↑ . PubChem. Retrieved . wikidata.org.
  6. [8] ↑ . ChemIDplus. Retrieved . chem.sis.nlm.nih.gov. Provenance: wikidata.org.
  7. [9] ↑ . PubChem. Retrieved . wikidata.org.
  8. [10] ↑ . wikidata.org.
  9. [11] ↑ . Gene Ontology release 2020-05-02. wikidata.org.
  10. [12] ↑ . wikidata.org.
  11. [13] ↑ . ChEMBL. Retrieved . wikidata.org.
  12. [14] ↑ . Freebase Data Dumps. wikidata.org.
  13. [15] ↑ . Q2311683. Retrieved . wikidata.org.
  14. [16] ↑ . PubChem. Retrieved . wikidata.org.
  15. [17] ↑ . ChEBI. Retrieved . wikidata.org.
  16. [18] ↑ . ChEBI. Retrieved . wikidata.org.
  17. [19] ↑ . ChEBI. Retrieved . wikidata.org.
  18. [20] ↑ . Chemical examination of the roots of Terminalia arjuna—the structures of arjunoside III and arjunoside IV, two new triterpenoid glycosides. wikidata.org.
  19. [21] ↑ . Evidence for oxidation at C-3 of the flavonoid C-ring during anthocyanin biosynthesis. wikidata.org.
  20. [22] ↑ . A Phytochemical Study of Some Cassia Species Cultivated in Egypt. wikidata.org.
  21. [23] ↑ . Phenolic compounds of the plantGossypium hirsutum and of callus tissue from its anthers. wikidata.org.
  22. [24] ↑ . Proanthocyanidins of Polygonum coriarium. I. wikidata.org.
  23. [25] ↑ . Enzymatic reduction of (+)-dihydroflavonols to flavan-3,4-cis-diols with flower extracts from Matthiola incana and its role in anthocyanin biosynthesis. wikidata.org.
  24. [26] ↑ . ChEBI. Retrieved . 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). (2R,3S,4S)-leucocyanidin. Retrieved May 3, 2026, from https://4ort.xyz/entity/2r-3s-4s-leucocyanidin
MLA “(2R,3S,4S)-leucocyanidin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/2r-3s-4s-leucocyanidin.
BibTeX @misc{4ortxyz_2r-3s-4s-leucocyanidin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{(2R,3S,4S)-leucocyanidin}}, year = {2026}, url = {https://4ort.xyz/entity/2r-3s-4s-leucocyanidin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): (2R,3S,4S)-leucocyanidin — https://4ort.xyz/entity/2r-3s-4s-leucocyanidin (retrieved 2026-05-03)

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