Gyrophoric acid

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 ;
3D model (JSmol)	Interactive image;
ChEMBL	ChEMBL470648 ;
ChemSpider	119550 ;
PubChem CID	135728;
UNII	BAQ44A6C6H ;
CompTox Dashboard (EPA)	DTXSID30203289 ;
	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) Key: ATQPZSQVWCPVGV-UHFFFAOYSA-N ;
	SMILES 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). verify (what is ?) Infobox references

Gyrophoric acid is a depside 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]

References

^ 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
^ Casselman, Karen Leigh (1994). "Lichen Dyes: Preparation and Dyeing". Maine Naturalist. 2 (2): 105–110. doi:10.2307/3858253. ISSN 1063-3626.

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