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sophoraflavanone B

chemical compound
Class type of: 8C-prenylflavanone Q4644281

Facts

8 properties
Instance of
type of chemical entity
Subclass of
8C-prenylflavanone
Canonical SMILES
CC(=CCC1=C(C=C(C2=C1OC(CC2=O)C3=CC=C(C=C3)O)O)O)C
Chemical formula
C₂₀H₂₀O₅
Found in taxon
Humulus lupulus, Flourensia riparia, Glycyrrhiza uralensis, Macaranga conifera, Sophora moorcroftiana, Sophora tomentosa, Glycosmis chlorosperma, Sophora flavescens, Azadirachta indica, Helichrysum athrixiifolium, Maclura pomifera, Marshallia mohrii, Marshallia graminifolia, Vernonia angustifolia, Wyethia angustifolia, Wyethia glabra, Wyethia mollis, Scabrethia scabra, Sophora leachiana, Macaranga denticulata, Maclura cochinchinensis
Isomeric SMILES
CC(=CCC1=C(C=C(C2=C1O[C@@H](CC2=O)C3=CC=C(C=C3)O)O)O)C
Mass
+340.131074
Physically interacts with
taste receptor type 2
🏷️ Also known as
en (-)-(2S)-5,7-dihydroxy-2-(4-hydroxyphenyl)-8-(3-methylbut-2-enyl)chroman-4-one en (-)-(2S)-8-dimethylallylnaringenin en 8-PN en 8-prenylnaringenin en 8-Prenylnaringenin en Flavaprenin en (S)-8-dimethylallylnaringenin en sophoraflavanone B en Sophoraflavanone B es 8-prenilnaringenina fr 8-prénylnaringinine ja ソホラフラバノンB zh 8-异戊烯基柚皮素
🔖 Identifiers · 20
CAS Registry Number
53846-50-7
ChEBI ID
50207
ChEMBL ID
CHEMBL376915
ChemSpider ID
421848
DSSTOX compound identifier
DTXCID90284175
DSSTox substance ID
DTXSID60333083
Freebase ID
/m/0pl242h
InChI
InChI=1S/C20H20O5/c1-11(2)3-8-14-15(22)9-16(23)19-17(24)10-18(25-20(14)19)12-4-6-13(21)7-5-12/h3-7,9,18,21-23H,8,10H2,1-2H3/t18-/m0/s1
InChIKey
LPEPZZAVFJPLNZ-SFHVURJKSA-N
KEGG ID
C18023
LIPID MAPS ID
LMPK12140279
MassBank accession ID
MSBNK-BS-BS003000, MSBNK-BS-BS003001, MSBNK-BS-BS003002, MSBNK-BS-BS003003
Show all 20 identifiers +8
Microsoft Academic ID (discontinued)
2780221043
Probes And Drugs ID
PD017477
PubChem CID
480764
Reaxys registry number
5611472
SPLASH
splash10-000i-0039000000-1a68000feccaaebcdb67, splash10-000i-0009000000-511c5eba590f52e7c5ac, splash10-014i-0930000000-4487926a00e47414c95a
SureChEMBL ID
29396586, 1171435
UNII
5L872SZR8X
UniChem compound ID
467660

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🔗 Connections
Found in taxon 18
Azadirachta indica, Humulus lupulus, Maclura pomifera, Glycyrrhiza uralensis, Sophora tomentosa, Sophora flavescens, Macaranga denticulata, Maclura cochinchinensis +10 more
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Summary

sophoraflavanone B is a type of chemical entity[1]. It is a type of 8C-prenylflavanone[2].

Key Facts

  • Physically interacts with: taste receptor type 2[3]
  • Canonical SMILES: CC(=CCC1=C(C=C(C2=C1OC(CC2=O)C3=CC=C(C=C3)O)O)O)C[4]
  • Chemical formula: C₂₀H₂₀O₅[5]
  • Found in taxon: Humulus lupulus[6], Flourensia riparia[7], Glycyrrhiza uralensis[8], Macaranga conifera[9], Sophora moorcroftiana[10], Sophora tomentosa[11], Glycosmis chlorosperma[12], Sophora flavescens[13], Azadirachta indica[14], Helichrysum athrixiifolium[15], Maclura pomifera[16], Marshallia mohrii[17], Marshallia graminifolia[18], Vernonia angustifolia[19]
  • Isomeric SMILES: CC(=CCC1=C(C=C(C2=C1OC@@HC3=CC=C(C=C3)O)O)O)CC@@HC3=CC=C(C=C3)O)O)O)C">[20]
  • Mass: 340.131074 dalton[21]

References

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

Direct Wikidata claims

  1. [3] ↑ . The bitter pill: clinical drugs that activate the human bitter taste receptor TAS2R14.. wikidata.org.
  2. [4] ↑ . PubChem. Retrieved . wikidata.org.
  3. [5] ↑ . PubChem. Retrieved . wikidata.org.
  4. [2] ↑ . wikidata.org.
  5. [6] ↑ . Regulation of osteoblastic phenotype and gene expression by hop-derived phytoestrogens.. wikidata.org.
  6. [7] ↑ . Constituents of two Flourensia species. wikidata.org.
  7. [8] ↑ . Field Survey of Glycyrrhiza Plants in Central Asia (2)1). Characterization of Phenolics and Their Variation in the Leaves of Glycyrrhiza Plants Collected in Kazakhstan. wikidata.org.
  8. [9] ↑ . Prenylated flavonoids of the leaves of Macaranga conifera with inhibitory activity against cyclooxygenase-2.. wikidata.org.
  9. [10] ↑ . Studies on the constituents of Sophora species. XXII. Constituents of the root of Sophora moorcroftiana BENTH. ex BAKER.(1).. wikidata.org.
  10. [11] ↑ . Studies on the constituents of sophora species. XIII. Constituents of the aerial parts of Sophora tomentosa L. wikidata.org.
  11. [12] ↑ . Prenylated flavanones and flavanonols as chemical markers in Glycosmis species (Rutaceae).. wikidata.org.
  12. [13] ↑ . Efficient production and capture of 8-prenylnaringenin and leachianone G-biosynthetic intermediates of sophoraflavanone G--by the addition of cork tissue to cell suspension cultures of Sophora flavescens. wikidata.org.
  13. [14] ↑ . Prenylated Flavanones Isolated from Flowers of Azadirachta indica (the Neem Tree) as Antimutagenic Constituents against Heterocyclic Amines. wikidata.org.
  14. [15] ↑ . Three prenylated flavanoids from Helichrysum athrixiifolium. wikidata.org.
  15. [16] ↑ . Comparison between metabolite productions in cell culture and in whole plant of Maclura pomifera. wikidata.org.
  16. [17] ↑ . Prenyl flavanes from Marshallia species. wikidata.org.
  17. [18] ↑ . Prenyl flavanes from Marshallia species. wikidata.org.
  18. [19] ↑ . Prenyl flavanes from Marshallia species. wikidata.org.
  19. [20] ↑ . PubChem. Retrieved . wikidata.org.
  20. [21] ↑ . PubChem. Retrieved . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

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APA 4ort.xyz Knowledge Graph. (2026). sophoraflavanone B. Retrieved November 10, 2026, from https://4ort.xyz/entity/sophoraflavanone-b
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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 · Shuaib-bot bot · 2026-05-06 view diff on Wikidata ↗
    Found in taxon → Humulus lupulus, Flourensia riparia, Glycyrrhiza uralensis +1
    Subclass of → 8C-prenylflavanone
    Mass → 340.131074 dalton
    Physically interacts with → taste receptor type 2
    + 1 other property edited (see Wikidata diff for full list)
    "Changed the item"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.