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dihydromyricetin (unspecified stereochemistry)

chemical compound
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dihydromyricetin (unspecified stereochemistry)

Summary

dihydromyricetin (unspecified stereochemistry) is a group of isomeric entities[1].

Key Facts

  • dihydromyricetin (unspecified stereochemistry)'s instance of is recorded as group of isomeric entities[2].
  • dihydromyricetin (unspecified stereochemistry)'s canonical SMILES is recorded as C1=C(C=C(C(=C1O)O)O)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O[3].
  • dihydromyricetin (unspecified stereochemistry)'s chemical formula is recorded as C₁₅H₁₂O₈[4].
  • dihydromyricetin (unspecified stereochemistry) is a type of dihydroxyflavanone[5].
  • dihydromyricetin (unspecified stereochemistry)'s found in taxon is recorded as Syzygium[6].
  • dihydromyricetin (unspecified stereochemistry)'s found in taxon is recorded as Intsia[7].
  • dihydromyricetin (unspecified stereochemistry)'s found in taxon is recorded as Rhododendron cinnabarinum[8].
  • dihydromyricetin (unspecified stereochemistry)'s found in taxon is recorded as Manilkara[9].
  • dihydromyricetin (unspecified stereochemistry)'s found in taxon is recorded as Cedrus deodara[10].
  • dihydromyricetin (unspecified stereochemistry)'s mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+320.053217'}[11].

Body

Definition and Type

dihydromyricetin (unspecified stereochemistry)'s instance of is recorded as group of isomeric entities[2]. dihydromyricetin (unspecified stereochemistry) is a type of dihydroxyflavanone[5].

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] ↑ . wikidata.org.
  5. [6] ↑ . Syzygium cumini (L.) Skeels: A review of its phytochemical constituents and traditional uses. wikidata.org.
  6. [7] ↑ . Polyphenols of Intsia heartwoods. wikidata.org.
  7. [8] ↑ . Leaf survey of flavonoids and simple phenols in the genus Rhododendron. wikidata.org.
  8. [9] ↑ . Bioactive novel polyphenols from the fruit of Manilkara zapota (Sapodilla).. wikidata.org.
  9. [10] ↑ . Two new myricetin glycosides from pine needles of Cedrus deodara. wikidata.org.
  10. [11] ↑ . PubChem. 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). dihydromyricetin (unspecified stereochemistry). Retrieved May 3, 2026, from https://4ort.xyz/entity/dihydromyricetin-unspecified-stereochemistry-
MLA “dihydromyricetin (unspecified stereochemistry).” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/dihydromyricetin-unspecified-stereochemistry-.
BibTeX @misc{4ortxyz_dihydromyricetin-unspecified-stereochemistry-_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{dihydromyricetin (unspecified stereochemistry)}}, year = {2026}, url = {https://4ort.xyz/entity/dihydromyricetin-unspecified-stereochemistry-}, note = {Accessed: 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. 11d ago · Nabbegat · 2026-06-19 view diff on Wikidata ↗
    Dsstox substance id → DTXSID001347411
    Probes and drugs id → PD056519
    Imported from → —
    Instance of → group of isomeric entities
    + 15 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update-languages-short:0||tr */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/37300|batch #37300]]"
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