tricin 7-O-glucoside

chemical compound
ChemicalSubstance group_of_stereoisomers Q27145235
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Summary

tricin 7-O-glucoside is a group of stereoisomers[1].

Key Facts

  • tricin 7-O-glucoside's instance of is recorded as group of stereoisomers[2].
  • tricin 7-O-glucoside's canonical SMILES is recorded as COC1=CC(=CC(=C1O)OC)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O[3].
  • tricin 7-O-glucoside's InChI is recorded as InChI=1S/C23H24O12/c1-31-15-3-9(4-16(32-2)19(15)27)13-7-12(26)18-11(25)5-10(6-14(18)34-13)33-23-22(30)21(29)20(28)17(8-24)35-23/h3-7,17,20-25,27-30H,8H2,1-2H3/t17-,20-,21+,22-,23?/m1/s1[4].
  • tricin 7-O-glucoside's InChIKey is recorded as JGXFMIJHKASCIZ-NODAHLOSSA-N[5].
  • tricin 7-O-glucoside's chemical formula is recorded as C₂₃H₂₄O₁₂[6].
  • tricin 7-O-glucoside's subclass of is recorded as chemical compound[7].
  • tricin 7-O-glucoside's ChemSpider ID is recorded as 29368527[8].
  • tricin 7-O-glucoside's PubChem CID is recorded as 13984470[9].
  • tricin 7-O-glucoside's ChEBI ID is recorded as 75349[10].
  • tricin 7-O-glucoside's found in taxon is recorded as Lonicera japonica[11].
  • tricin 7-O-glucoside's Reaxys registry number is recorded as 5785058[12].
  • tricin 7-O-glucoside's isomeric SMILES is recorded as COC1=CC(=CC(=C1O)OC)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C@@HO)OC@@HO)O">[13].
  • tricin 7-O-glucoside's Human Metabolome Database ID is recorded as HMDB0030553[14].
  • tricin 7-O-glucoside's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+492.126776'}[15].
  • tricin 7-O-glucoside's SureChEMBL ID is recorded as 6876130[16].
  • tricin 7-O-glucoside's UniChem compound ID is recorded as 63002659[17].

References

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

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . PubChem. Retrieved . wikidata.org.
  3. [4] ↑ . PubChem. Retrieved . wikidata.org.
  4. [5] ↑ . PubChem. Retrieved . wikidata.org.
  5. [6] ↑ . PubChem. Retrieved . wikidata.org.
  6. [7] ↑ . wikidata.org.
  7. [8] ↑ . ChemSpider. Retrieved . wikidata.org.
  8. [9] ↑ . PubChem. Retrieved . wikidata.org.
  9. [10] ↑ . ChEBI. Retrieved . wikidata.org.
  10. [11] ↑ . Capillary high-performance liquid chromatography with mass spectrometry for simultaneous determination of major flavonoids, iridoid glucosides and saponins in Flos Lonicerae. wikidata.org.
  11. [12] ↑ . ChEBI. Retrieved . wikidata.org.
  12. [13] ↑ . PubChem. Retrieved . wikidata.org.
  13. [14] ↑ . wikidata.org.
  14. [15] ↑ . PubChem. Retrieved . wikidata.org.
  15. [16] ↑ . wikidata.org.
  16. [17] ↑ . UniChem. 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). tricin 7-O-glucoside. Retrieved May 3, 2026, from https://4ort.xyz/entity/tricin-7-o-glucoside
MLA “tricin 7-O-glucoside.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/tricin-7-o-glucoside.
BibTeX @misc{4ortxyz_tricin-7-o-glucoside_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{tricin 7-O-glucoside}}, year = {2026}, url = {https://4ort.xyz/entity/tricin-7-o-glucoside}, note = {Accessed: 2026-05-03}}
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