Hispidin

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Hispidin
Chemical structure of hispidin
Chemical structure of hispidin
Names
Preferred IUPAC name
6-[(1E)-2-(3,4-Dihydroxyphenyl)ethen-1-yl]-4-hydroxy-2H-pyran-2-one
Other names
6-(3,4-Dihydroxystyryl)-4-hydroxy-2-pyrone
Identifiers
3D model (JSmol)
ChemSpider
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UNII
  • {{#property:P3117}}Lua error in Module:EditAtWikidata at line 29: attempt to index field 'wikibase' (a nil value).
  • InChI=1S/C13H10O5/c14-9-6-10(18-13(17)7-9)3-1-8-2-4-11(15)12(16)5-8/h1-7,14-16H/b3-1+ N
    Key: SGJNQVTUYXCBKH-HNQUOIGGSA-N N
  • C1=CC(=C(C=C1/C=C/C2=CC(=CC(=O)O2)O)O)O
  • OC=2/C=C(/C=C/c1ccc(O)c(O)c1)OC(=O)C=2
Properties
C13H10O5
Molar mass 246.218 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Hispidin is a natural substance. It can also be synthesized.[1]

Hispidin 4-O-β-D-glucopyranoside can be found in Pteris ensiformis[2] whereas hispidin derivatives, such as phellibaumins, can be found in the edible mushroom Inonotus xeranticus[3] or Phellinus.[4][5] Hispidin is a precursor of fungal luciferin, a compound responsible for light emission by luminous mushrooms.

See also

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References

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