Cinnamoside

group of stereoisomers with the chemical formula C₂₄H₃₈O₁₂
ChemicalSubstance group_of_stereoisomers Q105304461
Press Enter · cited answer in seconds

Cinnamoside

Summary

Cinnamoside is a group of stereoisomers[1].

Key Facts

  • Cinnamoside's instance of is recorded as group of stereoisomers[2].
  • Cinnamoside's CAS Registry Number is recorded as 108567-70-0[3].
  • Cinnamoside's canonical SMILES is recorded as O=C(C=C=C1C(O)(C)CC(OC2OC(COC3OCC(O)(CO)C3O)C(O)C(O)C2O)CC1(C)C)C[4].
  • Cinnamoside's InChI is recorded as InChI=1S/C24H38O12/c1-12(26)5-6-15-22(2,3)7-13(8-23(15,4)31)35-20-18(29)17(28)16(27)14(36-20)9-33-21-19(30)24(32,10-25)11-34-21/h5,13-14,16-21,25,27-32H,7-11H2,1-4H3[5].
  • Cinnamoside's InChIKey is recorded as WGFLJEFKPRMWSU-UHFFFAOYSA-N[6].
  • Cinnamoside's chemical formula is recorded as C₂₄H₃₈O₁₂[7].
  • Cinnamoside's subclass of is recorded as megastigmane[8].
  • Cinnamoside's PubChem CID is recorded as 13909547[9].
  • Cinnamoside's ChEBI ID is recorded as 169143[10].
  • Cinnamoside's found in taxon is recorded as Cinnamomum cassia[11].
  • Cinnamoside's found in taxon is recorded as Cinnamomum burmanni[12].
  • Cinnamoside's Human Metabolome Database ID is recorded as HMDB0038923[13].
  • Cinnamoside's KNApSAcK ID is recorded as C00054960[14].
  • Cinnamoside's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+518.236326656'}[15].
  • Cinnamoside's SureChEMBL ID is recorded as 29683359[16].
  • Cinnamoside's DSSTox substance ID is recorded as DTXSID101104018[17].
  • Cinnamoside's UniChem compound ID is recorded as 32002717[18].

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [2] . wikidata.org.
  2. [3] . Chemical Abstracts Service. Retrieved . wikidata.org.
  3. [4] . wikidata.org.
  4. [5] . wikidata.org.
  5. [6] . wikidata.org.
  6. [7] . wikidata.org.
  7. [8] . wikidata.org.
  8. [9] . PubChem. Retrieved . wikidata.org.
  9. [10] . ChEBI release 2022-06-13. wikidata.org.
  10. [11] . ChemInform Abstract: Structures of Potent Antiulcerogenic Compounds from Cinnamomum cassia.. wikidata.org.
  11. [12] . ChemInform Abstract: Structures of Potent Antiulcerogenic Compounds from Cinnamomum cassia.. wikidata.org.
  12. [13] . wikidata.org.
  13. [14] . wikidata.org.
  14. [15] . wikidata.org.
  15. [16] . wikidata.org.
  16. [17] . wikidata.org.
  17. [18] . UniChem. wikidata.org.

Class ancestry

  1. [1] . Wikidata. 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). Cinnamoside. Retrieved May 3, 2026, from https://4ort.xyz/entity/cinnamoside
MLA “Cinnamoside.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/cinnamoside.
BibTeX @misc{4ortxyz_cinnamoside_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Cinnamoside}}, year = {2026}, url = {https://4ort.xyz/entity/cinnamoside}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Cinnamoside — https://4ort.xyz/entity/cinnamoside (retrieved 2026-05-03)

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