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2,3-dihydroquercetin

group of stereoisomers with the chemical formula C₁₅H₁₂O₇
ChemicalSubstance group_of_stereoisomers Q104972046
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2,3-dihydroquercetin

Summary

2,3-dihydroquercetin is a group of stereoisomers[1].

Key Facts

  • 2,3-dihydroquercetin's instance of is recorded as group of stereoisomers[2].
  • 2,3-dihydroquercetin's canonical SMILES is recorded as O=C1C=2C(O)=CC(O)=CC2OC(C3=CC=C(O)C(O)=C3)C1O[3].
  • 2,3-dihydroquercetin's InChI is recorded as InChI=1S/C15H12O7/c16-7-4-10(19)12-11(5-7)22-15(14(21)13(12)20)6-1-2-8(17)9(18)3-6/h1-5,14-19,21H[4].
  • 2,3-dihydroquercetin's InChIKey is recorded as CXQWRCVTCMQVQX-UHFFFAOYSA-N[5].
  • 2,3-dihydroquercetin's chemical formula is recorded as C₁₅H₁₂O₇[6].
  • 2,3-dihydroquercetin's subclass of is recorded as flavanone[7].
  • 2,3-dihydroquercetin's PubChem CID is recorded as 471[8].
  • 2,3-dihydroquercetin's ChEBI ID is recorded as 38747[9].
  • 2,3-dihydroquercetin's found in taxon is recorded as Acacia adunca[10].
  • 2,3-dihydroquercetin's found in taxon is recorded as Excoecaria acerifolia[11].
  • 2,3-dihydroquercetin's found in taxon is recorded as Prunus lycioides[12].
  • 2,3-dihydroquercetin's found in taxon is recorded as Bidens parviflora[13].
  • 2,3-dihydroquercetin's found in taxon is recorded as Fagus grandifolia[14].
  • 2,3-dihydroquercetin's found in taxon is recorded as Eucalyptus melliodora[15].
  • 2,3-dihydroquercetin's found in taxon is recorded as Artemisia incanescens[16].
  • 2,3-dihydroquercetin's found in taxon is recorded as Thymus quinquecostatus[17].
  • 2,3-dihydroquercetin's found in taxon is recorded as Artemisia assoana[18].
  • 2,3-dihydroquercetin's found in taxon is recorded as Juglans nigra[19].
  • 2,3-dihydroquercetin's found in taxon is recorded as Eucalyptus apodophylla[20].
  • 2,3-dihydroquercetin's found in taxon is recorded as Thymus piperella[21].
  • 2,3-dihydroquercetin's found in taxon is recorded as Kadsura[22].
  • 2,3-dihydroquercetin's found in taxon is recorded as Polygala reinii[23].
  • 2,3-dihydroquercetin's found in taxon is recorded as Artemisia absinthium[24].
  • 2,3-dihydroquercetin's found in taxon is recorded as Nothofagus[25].
  • 2,3-dihydroquercetin's found in taxon is recorded as Garcinia brasiliensis[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 2021-03-01. wikidata.org.
  9. [10] ↑ . α-Amylase and lipase inhibitory activity and structural characterization of acacia bark proanthocyanidins. wikidata.org.
  10. [11] ↑ . Chemical constituents of Excoecaria acerifolia and their bioactivities. wikidata.org.
  11. [12] ↑ . Chiral flavanones from Amygdalus lycioides Spach: structural elucidation and identification of TNFalpha inhibitors by bioactivity-guided fractionation. wikidata.org.
  12. [13] ↑ . Flavonoids and a new polyacetylene from Bidens parviflora Willd.. wikidata.org.
  13. [14] ↑ . The extractives of New Zealand Nothofagus species. wikidata.org.
  14. [15] ↑ . Polyphenols and the Distribution of Arboreal, Folivorous Marsupials in Eucalyptus Forests of Australia. wikidata.org.
  15. [16] ↑ . Guaiane dimers and germacranolide from Artemisia caruifolia. wikidata.org.
  16. [17] ↑ . Isolation and structure elucidation of radical scavengers from Thymus vulgaris leaves.. wikidata.org.
  17. [18] ↑ . Guaiane dimers and germacranolide from Artemisia caruifolia. wikidata.org.
  18. [19] ↑ . Inhibition of human immunodeficiency virus type 1 reverse transcriptase and ribonuclease H activities by constituents of Juglans mandshurica. wikidata.org.
  19. [20] ↑ . Polyphenols and the Distribution of Arboreal, Folivorous Marsupials in Eucalyptus Forests of Australia. wikidata.org.
  20. [21] ↑ . Isolation and structure elucidation of radical scavengers from Thymus vulgaris leaves.. wikidata.org.
  21. [22] ↑ . Compounds from Kadsura heteroclita and related anti-HIV activity. wikidata.org.
  22. [23] ↑ . Xanthones from Polygala caudata. wikidata.org.
  23. [24] ↑ . Guaiane dimers and germacranolide from Artemisia caruifolia. wikidata.org.
  24. [25] ↑ . The extractives of New Zealand Nothofagus species. wikidata.org.
  25. [26] ↑ . Antibacterial and brine shrimp lethality tests of biflavonoids and derivatives of Rheedia gardneriana. wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

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