Variegatorubin

Variegatorubin
Names

IUPAC name (3E)-3-[4-(3,4-Dihydroxyphenyl)-3-hydroxy-5-oxo-2(5H)-furanylidene]-5,6-dihydroxy-1-benzofuran-2(3H)-one
Identifiers
CAS Number	27286-59-5^N
3D model (JSmol)	Interactive image
ChemSpider	52082514
PubChem CID	136247330
InChI InChI=1S/C18H10O9/c19-8-2-1-6(3-9(8)20)13-15(23)16(27-17(13)24)14-7-4-10(21)11(22)5-12(7)26-18(14)25/h1-5,19-23H/b16-14+ Key: UMIYSJROYJXHSW-JQIJEIRASA-N InChI=1/C18H10O9/c19-8-2-1-6(3-9(8)20)13-15(23)16(27-17(13)24)14-7-4-10(21)11(22)5-12(7)26-18(14)25/h1-5,19-23H/b16-14+ Key: UMIYSJROYJXHSW-JQIJEIRABG
SMILES c1cc(c(cc1C2=C(/C(=C\3/c4cc(c(cc4OC3=O)O)O)/OC2=O)O)O)O
Properties
Chemical formula	C₁₈H₁₀O₉
Molar mass	370.267
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Variegatorubin is a pulvinic acid derivative. It is a red pigment that is present in many members of the Boletales, an order of the division Basidiomycota. It is generated from the oxidation of variegatic acid. Bolete species that contain variegatorubin include Neoboletus luridiformis, Chalciporus piperatus, Rhizopogon roseolus, Exsudoporus frostii, Suillellus luridus, Rubroboletus rhodoxanthus, and R. satanas.^[1] Variegatorubin was discovered by Wolfgang Steglich and colleagues, and described as a new compound in 1970.^[2]

References

^ Gill, M.; Steglich, W. (2012). Pigments of Fungi (Macromycetes). Progress in the Chemistry of Organic Natural Products. Vol. 51. Springer Science & Business Media. pp. 1–297 (see p. 35). ISBN 978-3-7091-6971-1.
^ Steglich, W.; Furtner, W.; Prox, A. (1970). "Variegatorubin, an oxidation product of variegatic acid from Suillus piperatus (Bull. ex Fr.) O. Kuntze and other Boletaceae". Zeitschrift für Naturforschung B. 5: 557. doi:10.1515/znb-1970-0529. S2CID 95770276.

This page was last edited on 29 January 2023, at 06:05