D-(−)-salicin

chemical compound
ChemicalSubstance type_of_chemical_entity Q419173
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D-(−)-salicin

Summary

D-(−)-salicin is a type of chemical entity[1]. D-(−)-salicin has Wikipedia articles in 22 language editions, a strong signal of global cultural recognition.[2]

Key Facts

  • D-(−)-salicin's instance of is recorded as type of chemical entity[3].
  • D-(−)-salicin's physically interacts with is recorded as taste receptor type 2[4].
  • D-(−)-salicin's canonical SMILES is recorded as C1=CC=C(C(=C1)CO)OC2C(C(C(C(O2)CO)O)O)O[5].
  • D-(−)-salicin's chemical formula is recorded as C₁₃H₁₈O₇[6].
  • D-(−)-salicin is a type of primary alcohol[7].
  • D-(−)-salicin is a type of phenol glycoside[8].
  • D-(−)-salicin is a type of aromatic alcohol[9].
  • D-(−)-salicin is part of salicin transport[10].
  • D-(−)-salicin is part of salicin transmembrane transporter activity[11].
  • D-(−)-salicin is part of salicyl-alcohol beta-D-glucosyltransferase activity[12].
  • D-(−)-salicin's Commons category is recorded as Salicin[13].
  • D-(−)-salicin's found in taxon is recorded as Filipendula ulmaria[14].
  • D-(−)-salicin's found in taxon is recorded as Salix alba[15].
  • D-(−)-salicin's found in taxon is recorded as Q158590[16].
  • D-(−)-salicin's found in taxon is recorded as Salix phylicifolia[17].
  • D-(−)-salicin's found in taxon is recorded as Salix caprea[18].
  • D-(−)-salicin's found in taxon is recorded as Salix pentandra[19].
  • D-(−)-salicin's found in taxon is recorded as Salix lapponum[20].
  • D-(−)-salicin's found in taxon is recorded as Salix cinerea[21].
  • D-(−)-salicin's found in taxon is recorded as Salix aurita[22].
  • D-(−)-salicin's found in taxon is recorded as Salix triandra[23].
  • D-(−)-salicin's found in taxon is recorded as Salix fragilis[24].
  • D-(−)-salicin's found in taxon is recorded as Populus balsamifera[25].
  • D-(−)-salicin's found in taxon is recorded as Alangium chinense[26].
  • D-(−)-salicin's found in taxon is recorded as Alangium platanifolium[27].

Why It Matters

D-(−)-salicin has Wikipedia articles in 22 language editions, a strong signal of global cultural recognition.[2] D-(−)-salicin is known by 17 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] . The Molecular Receptive Ranges of Human TAS2R Bitter Taste Receptors. wikidata.org.
  3. [5] . PubChem. Retrieved . wikidata.org.
  4. [6] . PubChem. Retrieved . wikidata.org.
  5. [7] . wikidata.org.
  6. [8] . wikidata.org.
  7. [9] . wikidata.org.
  8. [10] . Gene Ontology release 2019-11-16. wikidata.org.
  9. [11] . Gene Ontology release 2019-11-16. wikidata.org.
  10. [12] . Gene Ontology release 2020-05-02. wikidata.org.
  11. [13] . wikidata.org.
  12. [14] . Filipendula ulmaria. wikidata.org.
  13. [15] . A chemotaxonomic survey of phenolics in leaves of northern salicaceae species. wikidata.org.
  14. [16] . A chemotaxonomic survey of phenolics in leaves of northern salicaceae species. wikidata.org.
  15. [17] . A chemotaxonomic survey of phenolics in leaves of northern salicaceae species. wikidata.org.
  16. [18] . A chemotaxonomic survey of phenolics in leaves of northern salicaceae species. wikidata.org.
  17. [19] . A chemotaxonomic survey of phenolics in leaves of northern salicaceae species. wikidata.org.
  18. [20] . A chemotaxonomic survey of phenolics in leaves of northern salicaceae species. wikidata.org.
  19. [21] . A chemotaxonomic survey of phenolics in leaves of northern salicaceae species. wikidata.org.
  20. [22] . A chemotaxonomic survey of phenolics in leaves of northern salicaceae species. wikidata.org.
  21. [23] . A chemotaxonomic survey of phenolics in leaves of northern salicaceae species. wikidata.org.
  22. [24] . A chemotaxonomic survey of phenolics in leaves of northern salicaceae species. wikidata.org.
  23. [25] . A chemotaxonomic survey of phenolics in leaves of northern salicaceae species. wikidata.org.
  24. [26] . Two new phenolic glycosides fromInula cappaDC. wikidata.org.
  25. [27] . Alangifolioside, a diphenylmethylene derivative, and other phenolics from the leaves of Alangium platanifolium var. trilobum. 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.

📑 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). D-(−)-salicin. Retrieved May 3, 2026, from https://4ort.xyz/entity/d-salicin
MLA “D-(−)-salicin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/d-salicin.
BibTeX @misc{4ortxyz_d-salicin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{D-(−)-salicin}}, year = {2026}, url = {https://4ort.xyz/entity/d-salicin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): D-(−)-salicin — https://4ort.xyz/entity/d-salicin (retrieved 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. 16d ago · Nabbegat · 2026-06-19 view diff on Wikidata ↗
    Stereoisomer of (2S,3R,4R,5S,6R)-2-(hydroxymethyl)-6-[2-(hydroxymethyl)phenoxy]oxane-3,4,5-triol, (2S,3R,4S,5R,6S)-2-(hydroxymethyl)-6-[2-(hydroxymethyl)phenoxy]oxane-3,4,5-triol
    Instance of type of chemical entity
    Has characteristic bitterness
    Part of
    + 11 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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