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diosmine

group of stereoisomers with the chemical formula C₂₈H₃₂O₁₅
ChemicalSubstance group_of_stereoisomers Q104395685
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diosmine

Summary

diosmine is a group of stereoisomers[1].

Key Facts

  • diosmine's instance of is recorded as group of stereoisomers[2].
  • diosmine's canonical SMILES is recorded as O=C1C=C(OC2=CC(OC3OC(COC4OC(C)C(O)C(O)C4O)C(O)C(O)C3O)=CC(O)=C12)C=5C=CC(OC)=C(O)C5[3].
  • diosmine's InChI is recorded as InChI=1S/C28H32O15/c1-10-21(32)23(34)25(36)27(40-10)39-9-19-22(33)24(35)26(37)28(43-19)41-12-6-14(30)20-15(31)8-17(42-18(20)7-12)11-3-4-16(38-2)13(29)5-11/h3-8,10,19,21-30,32-37H,9H2,1-2H3[4].
  • diosmine's InChIKey is recorded as GZSOSUNBTXMUFQ-UHFFFAOYSA-N[5].
  • diosmine's chemical formula is recorded as C₂₈H₃₂O₁₅[6].
  • diosmine's subclass of is recorded as flavone[7].
  • diosmine's PubChem CID is recorded as 5353588[8].
  • diosmine's ChEBI ID is recorded as 176381[9].
  • diosmine's found in taxon is recorded as Valeriana rossica[10].
  • diosmine's found in taxon is recorded as Scutellaria baicalensis[11].
  • diosmine's found in taxon is recorded as Pratia[12].
  • diosmine's found in taxon is recorded as Lobelia[13].
  • diosmine's found in taxon is recorded as Rosmarinus officinalis[14].
  • diosmine's Human Metabolome Database ID is recorded as HMDB0029548[15].
  • diosmine's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+608.174120324'}[16].
  • diosmine's SureChEMBL ID is recorded as 14178901[17].
  • diosmine's DSSTox substance ID is recorded as DTXSID10859445[18].
  • diosmine's MassBank accession ID is recorded as MSBNK-RIKEN-PR309440[19].
  • diosmine's MassBank accession ID is recorded as MSBNK-RIKEN-PR306212[20].
  • diosmine's MassBank accession ID is recorded as MSBNK-RIKEN-PR306218[21].
  • diosmine's MassBank accession ID is recorded as MSBNK-RIKEN-PR306224[22].
  • diosmine's MassBank accession ID is recorded as MSBNK-RIKEN-PR306230[23].
  • diosmine's MassBank accession ID is recorded as MSBNK-RIKEN-PR306236[24].
  • diosmine's MassBank accession ID is recorded as MSBNK-RIKEN-PR306242[25].
  • diosmine's MassBank accession ID is recorded as MSBNK-RIKEN-PR306248[26].

References

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

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . wikidata.org.
  3. [4] ↑ . wikidata.org.
  4. [5] ↑ . wikidata.org.
  5. [6] ↑ . wikidata.org.
  6. [7] ↑ . wikidata.org.
  7. [8] ↑ . PubChem. Retrieved . wikidata.org.
  8. [9] ↑ . ChEBI release 2022-06-13. wikidata.org.
  9. [10] ↑ . Phenolic compounds, sterols, and iridoids of valerian. VII. Composition of the phenolic compounds, β-sitosterol, and valepotriates ofValeriana rossica. wikidata.org.
  10. [11] ↑ . Inhibitory effect of baicalein on IL-6-mediated signaling cascades in human myeloma cells. wikidata.org.
  11. [12] ↑ . Polyacetylene glycosides from Pratia nummularia cultures. wikidata.org.
  12. [13] ↑ . Polyacetylene glycosides from Pratia nummularia cultures. wikidata.org.
  13. [14] ↑ . Flavonoid distribution during the development of leaves, flowers, stems, and roots of Rosmarinus officinalis. postulation of a biosynthetic pathway. wikidata.org.
  14. [15] ↑ . wikidata.org.
  15. [16] ↑ . wikidata.org.
  16. [17] ↑ . wikidata.org.
  17. [18] ↑ . wikidata.org.
  18. [19] ↑ . MassBank/MassBank-data: release version 2022.06 to wikidata. Retrieved . wikidata.org.
  19. [20] ↑ . MassBank/MassBank-data: release version 2022.06 to wikidata. Retrieved . wikidata.org.
  20. [21] ↑ . MassBank/MassBank-data: release version 2022.06 to wikidata. Retrieved . wikidata.org.
  21. [22] ↑ . MassBank/MassBank-data: release version 2022.06 to wikidata. Retrieved . wikidata.org.
  22. [23] ↑ . MassBank/MassBank-data: release version 2022.06 to wikidata. Retrieved . wikidata.org.
  23. [24] ↑ . MassBank/MassBank-data: release version 2022.06 to wikidata. Retrieved . wikidata.org.
  24. [25] ↑ . MassBank/MassBank-data: release version 2022.06 to wikidata. Retrieved . wikidata.org.
  25. [26] ↑ . MassBank/MassBank-data: release version 2022.06 to wikidata. Retrieved . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

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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). diosmine. Retrieved May 3, 2026, from https://4ort.xyz/entity/diosmine
MLA “diosmine.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/diosmine.
BibTeX @misc{4ortxyz_diosmine_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{diosmine}}, year = {2026}, url = {https://4ort.xyz/entity/diosmine}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): diosmine — https://4ort.xyz/entity/diosmine (retrieved 2026-05-03)

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