(R)-prunasin

chemical compound
ChemicalSubstance type_of_chemical_entity Q7253027
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(R)-prunasin

Summary

(R)-prunasin is a type of chemical entity[1]. (R)-prunasin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (27 views/month).[2]

Key Facts

  • (R)-prunasin's instance of is recorded as type of chemical entity[3].
  • (R)-prunasin's chemical structure is recorded as Prunasin.svg[4].
  • (R)-prunasin's CAS Registry Number is recorded as 99-18-3[5].
  • (R)-prunasin's EC number is recorded as 202-738-0[6].
  • (R)-prunasin's canonical SMILES is recorded as C1=CC=C(C=C1)C(C#N)OC2C(C(C(C(O2)CO)O)O)O[7].
  • (R)-prunasin's InChI is recorded as InChI=1S/C14H17NO6/c15-6-9(8-4-2-1-3-5-8)20-14-13(19)12(18)11(17)10(7-16)21-14/h1-5,9-14,16-19H,7H2/t9-,10+,11+,12-,13+,14+/m0/s1[8].
  • (R)-prunasin's InChIKey is recorded as ZKSZEJFBGODIJW-GMDXDWKASA-N[9].
  • (R)-prunasin's chemical formula is recorded as C₁₄H₁₇NO₆[10].
  • (R)-prunasin's subclass of is recorded as carbohydrate[11].
  • (R)-prunasin's part of is recorded as amygdalin beta-glucosidase activity[12].
  • (R)-prunasin's part of is recorded as prunasin beta-glucosidase activity[13].
  • (R)-prunasin's Commons category is recorded as Prunasin[14].
  • (R)-prunasin's MeSH descriptor ID is recorded as C019063[15].
  • (R)-prunasin's has part is recorded as oxygen[16].
  • (R)-prunasin's has part is recorded as carbon[17].
  • (R)-prunasin's ChEMBL ID is recorded as CHEMBL1778417[18].
  • (R)-prunasin's Freebase ID is recorded as /m/0q39syg[19].
  • (R)-prunasin's UNII is recorded as 14W4BPM5FB[20].
  • (R)-prunasin's ChemSpider ID is recorded as 106360[21].
  • (R)-prunasin's PubChem CID is recorded as 119033[22].
  • (R)-prunasin's KEGG ID is recorded as C00844[23].
  • (R)-prunasin's ChEBI ID is recorded as 17396[24].
  • (R)-prunasin's found in taxon is recorded as Vauquelinia corymbosa[25].
  • (R)-prunasin's found in taxon is recorded as Pteridium aquilinum[26].
  • (R)-prunasin's found in taxon is recorded as Prunus armeniaca[27].

Why It Matters

(R)-prunasin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (27 views/month).[2] (R)-prunasin has Wikipedia articles in 9 language editions, a strong signal of global cultural recognition.[28] (R)-prunasin is known by 5 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] . Global Substance Registration System. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  4. [6] . Global Substance Registration System. Retrieved . wikidata.org.
  5. [7] . PubChem. 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] . Gene Ontology release 2020-05-02. wikidata.org.
  11. [13] . Gene Ontology release 2020-05-02. wikidata.org.
  12. [14] . wikidata.org.
  13. [15] . Medical Subject Headings. Retrieved . wikidata.org.
  14. [16] . wikidata.org.
  15. [17] . wikidata.org.
  16. [18] . ChEMBL. Retrieved . wikidata.org.
  17. [19] . wikidata.org.
  18. [20] . Global Substance Registration System. Retrieved . wikidata.org.
  19. [21] . Q2311683. Retrieved . wikidata.org.
  20. [22] . PubChem. Retrieved . wikidata.org.
  21. [23] . wikidata.org.
  22. [24] . ChEBI. Retrieved . wikidata.org.
  23. [25] . α-Glucosidase Inhibitors from Vauquelinia corymbosa. wikidata.org.
  24. [26] . A method for the practical quantification and kinetic evaluation of cyanogenesis in plant material. Application toPteridium aquilinum andPassiflora capsularis. wikidata.org.
  25. [27] . Quick screening of major constituents in plant tissue by temperature programmed fractionation mass spectrometry. 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). (R)-prunasin. Retrieved May 3, 2026, from https://4ort.xyz/entity/r-prunasin
MLA “(R)-prunasin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/r-prunasin.
BibTeX @misc{4ortxyz_r-prunasin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{(R)-prunasin}}, year = {2026}, url = {https://4ort.xyz/entity/r-prunasin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): (R)-prunasin — https://4ort.xyz/entity/r-prunasin (retrieved 2026-05-03)

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