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isosakuranetin

chemical compound
Class type of: flavanone Q3459109

Facts

8 properties
Instance of
type of chemical entity
Subclass of
flavanone[4]
Canonical SMILES
COC1=CC=C(C=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O[2]
Chemical formula
C₁₆H₁₄O₅[3]
Found in taxon
Populus grandidentata, Populus tremula, Populus tremuloides, Populus tristis, Populus laurifolia, Populus koreana, Populus suaveolens, Populus maximowiczii, Populus cathayana, Populus szechuanica, Bitter bush, Piper crassinervium, Artemisia campestris, Artemisia xanthochroa, Baccharis dracunculifolia, Baccharis pingraea, Baccharis salicifolia, Baccharis vaccinioides, Calceolaria hypericina, Clinopodium laxiflorum, Clinopodium umbrosum, Commiphora socotrana, Cyclotrichium niveum, Diplostephium cinereum, Dolichlasium lagascae, Eriodictyon californicum, Heteroplexis microcephala, Hypenia salzmannii, Lycium bridgesii, Phrodus bridgesii, Plazia daphnoides, Proustia cuneifolia, Prunus domestica, Tanacetum sibiricum, Wyethia angustifolia, Wyethia glabra, Wyethia helenioides, Baccharis leptocephala, Piper marginatum, Prunus leveilleana, Prunus verecunda, Vitex quinata, Ageratina altissima, Rosmarinus officinalis, Prunus serrulata var. pubescens, Citrus × paradisi, Prunus avium, Citrus reticulata, Citrus × deliciosa, Populus trichocarpa, Baccharis glutinosa, Xanthorrhoea preissii, Xanthorrhoea australis, Xanthorrhoea resinosa, Baccharis douglasii, Salvia officinalis[5][6][7][8][9][10][11][12][13][14][15][16][17][18]
Isomeric SMILES
COC1=CC=C(C=C1)[C@@H]2CC(=O)C3=C(C=C(C=C3O2)O)O[19]
Mass
+286.084124[20]
Stereoisomer of
(R)-Isosakuranetin
🏷️ Also known as
en isosakuranetin en naringenin 4'-methyl ether en (S)-2,3-dihydro-5,7-dihydroxy-2-(4-methoxyphenyl)-4H-1-benzopyran-4-one fa ایزوساکورانتین fr isosakuranétine it isosakuranetina ja イソサクラネチン zh 异樱花素

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🔗 Connections
Found in taxon 42
Citrus reticulata, Prunus avium, Citrus × paradisi, Prunus domestica, Populus tremula, Salvia officinalis, Populus tremuloides, Artemisia campestris +34 more
Subclass of 1
flavanone
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Summary

isosakuranetin is a type of chemical entity[1].

References

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

Direct Wikidata claims

  1. [2] ↑ . PubChem. Retrieved . wikidata.org.
  2. [3] ↑ . PubChem. Retrieved . wikidata.org.
  3. [4] ↑ . wikidata.org.
  4. [5] ↑ . Chemotaxonomy of section Leuce poplars by GC-MS of bud exudate. wikidata.org.
  5. [6] ↑ . Chemotaxonomy of section Leuce poplars by GC-MS of bud exudate. wikidata.org.
  6. [7] ↑ . Chemotaxonomy of section Leuce poplars by GC-MS of bud exudate. wikidata.org.
  7. [8] ↑ . Analysis of Phenolics of Bud Exudate of Populus tristis by GC/MS. wikidata.org.
  8. [9] ↑ . Notes: Analysis of Phenolics of Bud Exudate of Populus laurifolia by GC-MS. wikidata.org.
  9. [10] ↑ . Analysis of Phenolics of Bud Exudates of Populus koreana, Populus maximowiczii and Populus suaveolens by GC-MS. wikidata.org.
  10. [11] ↑ . Analysis of Phenolics of Bud Exudates of Populus koreana, Populus maximowiczii and Populus suaveolens by GC-MS. wikidata.org.
  11. [12] ↑ . Analysis of Phenolics of Bud Exudates of Populus koreana, Populus maximowiczii and Populus suaveolens by GC-MS. wikidata.org.
  12. [13] ↑ . Analysis of Phenolics of Bud Exudates of Populus cathayana and Populus szechuanica by GC-MS. wikidata.org.
  13. [14] ↑ . Analysis of Phenolics of Bud Exudates of Populus cathayana and Populus szechuanica by GC-MS. wikidata.org.
  14. [15] ↑ . Antimycobacterial activity and cytotoxicity of flavonoids from the flowers of Chromolaena odorata. wikidata.org.
  15. [16] ↑ . Benzoic acid derivatives from Piper species and their fungitoxic activity against Cladosporium cladosporioides and C. sphaerospermum. wikidata.org.
  16. [17] ↑ . A cadinane derivative from Artemisia crithmifolia. wikidata.org.
  17. [18] ↑ . Prenylated coumarates from Artemisia xanthochroa. wikidata.org.
  18. [19] ↑ . PubChem. Retrieved . wikidata.org.
  19. [20] ↑ . PubChem. Retrieved . 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). isosakuranetin. Retrieved November 11, 2026, from https://4ort.xyz/entity/isosakuranetin
MLA “isosakuranetin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 11 Nov. 2026, https://4ort.xyz/entity/isosakuranetin.
BibTeX @misc{4ortxyz_isosakuranetin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{isosakuranetin}}, year = {2026}, url = {https://4ort.xyz/entity/isosakuranetin}, note = {Accessed: 2026-11-11}}
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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. 27w ago · Michael D. Turnbull · 2026-05-06 view diff on Wikidata ↗
    Chemical structure → Isosakuranetin.svg
    "Created claim: Chemical structure: Isosakuranetin.svg"
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