5,7-dihydroxyflavanone

pair of isomers
ChemicalSubstance group_of_stereoisomers Q748200
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5,7-dihydroxyflavanone

Summary

5,7-dihydroxyflavanone is a group of stereoisomers[1].

Key Facts

  • 5,7-dihydroxyflavanone's instance of is recorded as group of stereoisomers[2].
  • 5,7-dihydroxyflavanone's chemical structure is recorded as Pinocembrin structure.svg[3].
  • 5,7-dihydroxyflavanone's canonical SMILES is recorded as O=C2c3c(OC(c1ccccc1)C2)cc(O)cc3O[4].
  • 5,7-dihydroxyflavanone's InChI is recorded as InChI=1S/C15H12O4/c16-10-6-11(17)15-12(18)8-13(19-14(15)7-10)9-4-2-1-3-5-9/h1-7,13,16-17H,8H2[5].
  • 5,7-dihydroxyflavanone's InChIKey is recorded as URFCJEUYXNAHFI-UHFFFAOYSA-N[6].
  • 5,7-dihydroxyflavanone's chemical formula is recorded as C₁₅H₁₂O₄[7].
  • 5,7-dihydroxyflavanone's subclass of is recorded as flavanone[8].
  • 5,7-dihydroxyflavanone's ChEMBL ID is recorded as CHEMBL399910[9].
  • 5,7-dihydroxyflavanone's ChemSpider ID is recorded as 208593[10].
  • 5,7-dihydroxyflavanone's PubChem CID is recorded as 238782[11].
  • 5,7-dihydroxyflavanone's found in taxon is recorded as Lychnophora ericoides[12].
  • 5,7-dihydroxyflavanone's found in taxon is recorded as Glycyrrhiza inflata[13].
  • 5,7-dihydroxyflavanone's found in taxon is recorded as Vachellia pennatula[14].
  • 5,7-dihydroxyflavanone's found in taxon is recorded as Boesenbergia[15].
  • 5,7-dihydroxyflavanone's found in taxon is recorded as Centaurea sonchifolia[16].
  • 5,7-dihydroxyflavanone's found in taxon is recorded as Uvaria lucida[17].
  • 5,7-dihydroxyflavanone's found in taxon is recorded as Centaurea scoparia[18].
  • 5,7-dihydroxyflavanone's found in taxon is recorded as Piper callosum[19].
  • 5,7-dihydroxyflavanone's found in taxon is recorded as Populus[20].
  • 5,7-dihydroxyflavanone's found in taxon is recorded as Piper nigrum[21].
  • 5,7-dihydroxyflavanone's found in taxon is recorded as Betula alnoides[22].
  • 5,7-dihydroxyflavanone's found in taxon is recorded as Helichrysum italicum[23].
  • 5,7-dihydroxyflavanone's found in taxon is recorded as Anomianthus dulcis[24].
  • 5,7-dihydroxyflavanone's found in taxon is recorded as Uvaria chamae[25].
  • 5,7-dihydroxyflavanone's found in taxon is recorded as Apis[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] . PubChem. wikidata.org.
  5. [6] . PubChem. wikidata.org.
  6. [7] . PubChem. wikidata.org.
  7. [8] . LIPID MAPS. wikidata.org.
  8. [9] . wikidata.org.
  9. [10] . wikidata.org.
  10. [11] . wikidata.org.
  11. [12] . Sesquiterpene lactones from Lychnophora ericoides.. wikidata.org.
  12. [13] . Structural study of glabrisoflavone, a novel isoflavone fromGlycyrrhiza glabra L.. wikidata.org.
  13. [14] . Variation in chemical composition, antibacterial and antioxidant activity of fresh and dried Acacia leaf extracts. wikidata.org.
  14. [15] . Medicinal foodstuffs. XXXIV. Structures of new prenylchalcones and prenylflavanones with TNF-alpha and aminopeptidase N inhibitory activities from Boesenbergia rotunda. wikidata.org.
  15. [16] . Biomimetic cyclization of cnicin to malacitanolide, a cytotoxic eudesmanolide from Centaurea malacitana. wikidata.org.
  16. [17] . New benzyldihydrochalcones from Uvaria chamae. wikidata.org.
  17. [18] . Biomimetic cyclization of cnicin to malacitanolide, a cytotoxic eudesmanolide from Centaurea malacitana. wikidata.org.
  18. [19] . Benzoic acid derivatives from Piper species and their fungitoxic activity against Cladosporium cladosporioides and C. sphaerospermum. wikidata.org.
  19. [20] . Die lipophilen flavonoide des knospenöls von Populus nigra. wikidata.org.
  20. [21] . Benzoic acid derivatives from Piper species and their fungitoxic activity against Cladosporium cladosporioides and C. sphaerospermum. wikidata.org.
  21. [22] . Ermanin, ein neuer natürlicher Kämpferol-methyläther aus dem knospenexkret von Betula ermani. wikidata.org.
  22. [23] . Flavonoids and terpenoids from Helichrysum forskahlii. wikidata.org.
  23. [24] . New benzyldihydrochalcones from Uvaria chamae. wikidata.org.
  24. [25] . New benzyldihydrochalcones from Uvaria chamae. wikidata.org.
  25. [26] . Effect of Pinocembrin Isolated from Mexican Brown Propolis on Diabetic Nephropathy. wikidata.org.

Class ancestry

  1. [1] . Wikidata. wikidata.org.

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APA 4ort.xyz Knowledge Graph. (2026). 5,7-dihydroxyflavanone. Retrieved May 3, 2026, from https://4ort.xyz/entity/5-7-dihydroxyflavanone
MLA “5,7-dihydroxyflavanone.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/5-7-dihydroxyflavanone.
BibTeX @misc{4ortxyz_5-7-dihydroxyflavanone_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{5,7-dihydroxyflavanone}}, year = {2026}, url = {https://4ort.xyz/entity/5-7-dihydroxyflavanone}, note = {Accessed: 2026-05-03}}
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