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rosarin

chemical compound
ChemicalSubstance type_of_chemical_entity Q15424778
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rosarin

Summary

rosarin is a type of chemical entity[1]. rosarin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (9 views/month).[2]

Key Facts

  • rosarin's instance of is recorded as type of chemical entity[3].
  • rosarin's chemical structure is recorded as Rosarin v2.svg[4].
  • rosarin's CAS Registry Number is recorded as 84954-93-8[5].
  • rosarin's canonical SMILES is recorded as C1=CC=C(C=C1)C=CCOC2C(C(C(C(O2)COC3C(C(C(O3)CO)O)O)O)O)O[6].
  • rosarin's InChI is recorded as InChI=1S/C20H28O10/c21-9-12-14(22)17(25)20(29-12)28-10-13-15(23)16(24)18(26)19(30-13)27-8-4-7-11-5-2-1-3-6-11/h1-7,12-26H,8-10H2/b7-4+/t12-,13+,14-,15+,16-,17+,18+,19+,20+/m0/s1[7].
  • rosarin's InChIKey is recorded as IEBFEMIXXHIISM-YZOUKVLTSA-N[8].
  • rosarin's chemical formula is recorded as C₂₀H₂₈O₁₀[9].
  • rosarin's subclass of is recorded as 2-[[3,4-Dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-(3-phenylprop-2-enoxy)oxane-3,4,5-triol[10].
  • rosarin's Commons category is recorded as Rosarin[11].
  • rosarin's Freebase ID is recorded as /m/0xnv8t1[12].
  • rosarin's UNII is recorded as PQA54L0KFI[13].
  • rosarin's ChemSpider ID is recorded as 8495834[14].
  • rosarin's PubChem CID is recorded as 10320370[15].
  • rosarin's ChEBI ID is recorded as 137499[16].
  • rosarin's found in taxon is recorded as Juniperus phoenicea[17].
  • rosarin's found in taxon is recorded as Rhodiola sachalinensis[18].
  • rosarin's found in taxon is recorded as Juniperus communis[19].
  • rosarin's found in taxon is recorded as Juniperus communis depressa[20].
  • rosarin's found in taxon is recorded as Rhodiola crenulata[21].
  • rosarin's found in taxon is recorded as Juniperus communis var. depressa[22].
  • rosarin's found in taxon is recorded as Rhodiola rosea[23].
  • rosarin's isomeric SMILES is recorded as C1=CC=C(C=C1)/C=C/CO[C@H]2C@@HOC@@HO">[24].
  • rosarin's mass is recorded as {'unit': 'Q483261', 'amount': '+428.168'}[25].
  • rosarin's SureChEMBL ID is recorded as 14705646[26].
  • rosarin's DSSTox substance ID is recorded as DTXSID601045580[27].

Why It Matters

rosarin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (9 views/month).[2]

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] ↑ . PubChem. Retrieved . wikidata.org.
  5. [7] ↑ . PubChem. Retrieved . wikidata.org.
  6. [8] ↑ . PubChem. Retrieved . wikidata.org.
  7. [9] ↑ . PubChem. Retrieved . wikidata.org.
  8. [10] ↑ . wikidata.org.
  9. [11] ↑ . wikidata.org.
  10. [12] ↑ . wikidata.org.
  11. [13] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  12. [14] ↑ . Q2311683. Retrieved . wikidata.org.
  13. [15] ↑ . PubChem. Retrieved . wikidata.org.
  14. [16] ↑ . ChEBI release 2019-10-02. wikidata.org.
  15. [17] ↑ . Phenylpropane Glycosides fromJuniperus phœnicea. wikidata.org.
  16. [18] ↑ . Prolyl endopeptidase inhibitors from the underground part of Rhodiola sachalinensis. wikidata.org.
  17. [19] ↑ . New Neolignan and Phenylpropanoid Glycosides in Juniperus communis var. depressa. wikidata.org.
  18. [20] ↑ . New Neolignan and Phenylpropanoid Glycosides in Juniperus communis var. depressa. wikidata.org.
  19. [21] ↑ . The chemotaxonomic classification of Rhodiola plants and its correlation with morphological characteristics and genetic taxonomy. wikidata.org.
  20. [22] ↑ . New Neolignan and Phenylpropanoid Glycosides in Juniperus communis var. depressa. wikidata.org.
  21. [23] ↑ . Prolyl endopeptidase inhibitors from the underground part of Rhodiola sachalinensis. wikidata.org.
  22. [24] ↑ . PubChem. Retrieved . wikidata.org.
  23. [25] ↑ . PubChem. Retrieved . wikidata.org.
  24. [26] ↑ . wikidata.org.
  25. [27] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . Wikimedia Foundation. dumps.wikimedia.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). rosarin. Retrieved May 3, 2026, from https://4ort.xyz/entity/rosarin
MLA “rosarin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/rosarin.
BibTeX @misc{4ortxyz_rosarin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{rosarin}}, year = {2026}, url = {https://4ort.xyz/entity/rosarin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): rosarin — https://4ort.xyz/entity/rosarin (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. 27d ago · Shuaib-bot bot · 2026-05-06 view diff on Wikidata ↗
    Stereoisomer of → [(Z)-3-Phenyl-2-propenyl]6-O-alpha-L-arabinofuranosyl-beta-D-glucopyranoside, (2R,3R,4S,5R,6R)-2-[[(2R,3S,4R,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-[(E)-3-phenylprop-2-enoxy]oxane-3,4,5-triol, (2R,3S,4S,5R,6R)-2-[[(2R,3S,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-[(E)-3-phenylprop-2-enoxy]oxane-3,4,5-triol
    Subclass of → 2-[[3,4-Dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-(3-phenylprop-2-enoxy)oxane-3,4,5-triol
    Aliases → —
    Subclass of → —
    + 4 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */"
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