Gyrophoric acid

Gyrophoric acid
Chemical structure of gyrophoric acid
Names
Preferred IUPAC name
4-({4-[(2,4-Dihydroxy-6-methylbenzoyl)oxy]-2-hydroxy-6-methylbenzoyl}oxy)-2-hydroxy-6-methylbenzoic acid
Identifiers
CAS Number
  • 548-89-0 checkY
3D model (JSmol)
  • Interactive image
ChEMBL
  • ChEMBL470648 checkY
ChemSpider
  • 119550 checkY
PubChem CID
  • 135728
UNII
  • BAQ44A6C6H checkY
CompTox Dashboard (EPA)
  • DTXSID30203289 Edit this at Wikidata
InChI
  • InChI=1S/C24H20O10/c1-10-4-13(25)7-16(26)20(10)23(31)34-15-6-12(3)21(18(28)9-15)24(32)33-14-5-11(2)19(22(29)30)17(27)8-14/h4-9,25-28H,1-3H3,(H,29,30) checkY
    Key: ATQPZSQVWCPVGV-UHFFFAOYSA-N checkY
  • O=C(Oc1cc(c(C(=O)O)c(O)c1)C)c3c(cc(OC(=O)c2c(cc(O)cc2O)C)cc3O)C
Properties
Chemical formula
 C24H20O10
Molar mass 468.414 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)
Infobox references
Chemical compound

Gyrophoric acid is a tridepside that can be found in the lichen Cryptothecia rubrocincta and in Xanthoparmelia pokomyi.[1] It can also be found in most of the species of the Actinogyra, Lasallia, and Umbilicaria genera.[2]

See also

  • Umbilicaric acid

References

  1. ^ Candan Mehmet, Yilmaz Meral, Tay Thrgay, Kivanc Merih and Türk Hayrettin (2006). "Antimicrobial activity of extracts of the lichen Xanthoparmelia pokomyi and its gyrophoric and stenosporic acid constituents". Zeitschrift für Naturforschung C. 61 (5–6): 319–323. doi:10.1515/znc-2006-5-603. PMID 16869486. S2CID 22255609.{{cite journal}}: CS1 maint: multiple names: authors list (link) INIST 17912298
  2. ^ Casselman, Karen Leigh (1994). "Lichen Dyes: Preparation and Dyeing". Maine Naturalist. 2 (2): 105–110. doi:10.2307/3858253. ISSN 1063-3626. JSTOR 3858253.
  • v
  • t
  • e