rosavin

chemical compound
ChemicalSubstance type_of_chemical_entity Q104389124
Press Enter · cited answer in seconds

rosavin

Summary

rosavin is a type of chemical entity[1]. rosavin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (33 views/month).[2]

Key Facts

  • rosavin's instance of is recorded as type of chemical entity[3].
  • rosavin's chemical structure is recorded as Rosavin.svg[4].
  • rosavin's CAS Registry Number is recorded as 84954-92-7[5].
  • rosavin's canonical SMILES is recorded as OC1COC(OCC2OC(OCC=CC=3C=CC=CC3)C(O)C(O)C2O)C(O)C1O[6].
  • rosavin's InChI is recorded as InChI=1S/C20H28O10/c21-12-9-28-19(17(25)14(12)22)29-10-13-15(23)16(24)18(26)20(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].
  • rosavin's InChIKey is recorded as RINHYCZCUGCZAJ-IPXOVKFZSA-N[8].
  • rosavin's chemical formula is recorded as C₂₀H₂₈O₁₀[9].
  • rosavin's subclass of is recorded as CID 53395247[10].
  • rosavin's Commons category is recorded as Rosavin[11].
  • rosavin's Freebase ID is recorded as /m/04gvm0l[12].
  • rosavin's UNII is recorded as 1R72C0ROME[13].
  • rosavin's PubChem CID is recorded as 9823887[14].
  • rosavin's ChEBI ID is recorded as 139523[15].
  • rosavin's found in taxon is recorded as Rhodiola rosea[16].
  • rosavin's found in taxon is recorded as Cinnamomum cassia[17].
  • rosavin's found in taxon is recorded as Bacopa monnieri[18].
  • rosavin's found in taxon is recorded as Juniperus communis[19].
  • rosavin's found in taxon is recorded as Juniperus communis depressa[20].
  • rosavin's found in taxon is recorded as Rhodiola sachalinensis[21].
  • rosavin's found in taxon is recorded as Rhodiola crenulata[22].
  • rosavin's found in taxon is recorded as Juniperus communis var. depressa[23].
  • rosavin's found in taxon is recorded as Cinnamomum burmanni[24].
  • rosavin's isomeric SMILES is recorded as O[C@H]1COC@@HC@H[C@H]1OC@@HC@H[C@H]1O">[25].
  • rosavin's mass is recorded as {'unit': 'Q483261', 'amount': '+428.168247096'}[26].
  • rosavin's SureChEMBL ID is recorded as 6441835[27].

Why It Matters

rosavin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (33 views/month).[2] rosavin has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[28]

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] . Chemical Abstracts Service. Retrieved . wikidata.org.
  4. [6] . wikidata.org.
  5. [7] . wikidata.org.
  6. [8] . wikidata.org.
  7. [9] . wikidata.org.
  8. [10] . wikidata.org.
  9. [11] . wikidata.org.
  10. [12] . Freebase Data Dumps. wikidata.org.
  11. [13] . wikidata.org.
  12. [14] . PubChem. Retrieved . wikidata.org.
  13. [15] . ChEBI release 2021-03-01. wikidata.org.
  14. [16] . Comparative study of Rhodiola preparations on behavioral despair of rats.. wikidata.org.
  15. [17] . Tyrosinase-inhibitory constituents from the twigs of Cinnamomum cassia. wikidata.org.
  16. [18] . Chemical constituents of Bacopa monnieri. 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] . Neuroprotective effects of constituents of the oriental crude drugs, Rhodiola sacra, R. sachalinensis and Tokaku-joki-to, against beta-amyloid toxicity, oxidative stress and apoptosis. wikidata.org.
  20. [22] . The chemotaxonomic classification of Rhodiola plants and its correlation with morphological characteristics and genetic taxonomy. wikidata.org.
  21. [23] . New Neolignan and Phenylpropanoid Glycosides in Juniperus communis var. depressa. wikidata.org.
  22. [24] . Tyrosinase-inhibitory constituents from the twigs of Cinnamomum cassia. wikidata.org.
  23. [25] . 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.
  2. [28] . Wikidata sitelinks. 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). rosavin. Retrieved May 3, 2026, from https://4ort.xyz/entity/rosavin
MLA “rosavin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/rosavin.
BibTeX @misc{4ortxyz_rosavin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{rosavin}}, year = {2026}, url = {https://4ort.xyz/entity/rosavin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): rosavin — https://4ort.xyz/entity/rosavin (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/rosavin · Last refreshed: