Kushenin

Kushenin
Chemical structure of kushenin
Names
IUPAC name
(6aR,11aR)-8-Methoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-3,9-diol
Identifiers
CAS Number
  • 99217-66-0 checkY
3D model (JSmol)
  • Interactive image
ChemSpider
  • 10289951
PubChem CID
  • 21676223
InChI
  • InChI=1S/C16H14O5/c1-19-15-5-10-11-7-20-13-4-8(17)2-3-9(13)16(11)21-14(10)6-12(15)18/h2-6,11,16-18H,7H2,1H3/t11-,16-/m0/s1
    Key: NYGZYUAVZPIKBZ-ZBEGNZNMSA-N
  • COC1=C(C=C2C(=C1)[C@@H]3COC4=C([C@@H]3O2)C=CC(=C4)O)O
Properties
Chemical formula
 C16H14O5
Molar mass 286.283 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
Chemical compound

Kushenin is a pterocarpan, a type of furano-isoflavonoid, found in Sophora flavescens.[1]

References

  1. ^ Yang, Ya-nan; Zhu, Hui; Yuan, Xiang; Zhang, Xu; Feng, Zi-ming; Jiang, Jian-shuang; Zhang, Pei-cheng (2021). "Seven new prenylated flavanones from the roots of Sophora flavescens and their anti-proliferative activities". Bioorganic Chemistry. 109: 104716. doi:10.1016/j.bioorg.2021.104716. PMID 33607362. S2CID 231970073.{{cite journal}}: CS1 maint: multiple names: authors list (link)
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Types of pterocarpans
Pterocarpans:
  • Erybraedin C
  • Erythrabyssin II
  • Folitenol
  • Glycinol
  • Maackiain
  • Orientanol A, B and C
  • Pisatin
  • Sophorol
  • Trifolirhizin
O-methylated
  • Kushenin
  • Medicarpin
  • Pterocarpin
Prenylated
  • Bitucarpin A and B
  • Glyceollidin I and II
  • Glyceollins (Glyceollin I, II, III and IV)
  • Glycyrrhizol A
  • Morisianine
  • Phaseolin
  • Striatine
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