Evernic acid

Last updated
Evernic acid
Evernic acid.svg
Names
IUPAC name
2-hydroxy-4-(2-hydroxy-4-methoxy-6-methylbenzoyl)oxy-6-methylbenzoic acid
Other names
NSC 81164 [1]
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.007.873 OOjs UI icon edit-ltr-progressive.svg
EC Number
  • 208-658-2
PubChem CID
UNII
  • InChI=1S/C17H16O7/c1-8-5-11(7-12(18)14(8)16(20)21)24-17(22)15-9(2)4-10(23-3)6-13(15)19/h4-7,18-19H,1-3H3,(H,20,21)
  • Key: GODLCSLPZIBRMG-UHFFFAOYSA-N
  • CC1=CC(=CC(=C1C(=O)OC2=CC(=C(C(=C2)C)C(=O)O)O)O)OC
Properties
C17H16O7
Molar mass 332.308 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Evernic acid is an organic compound and depside with the molecular formula C17H16O7. [2] Evernic acid was first isolated from the lichen Usnea longissima . [3] [4] Evernic acid is soluble in hot alcohol and poorly soluble in water. [5] [6] [7] Evernic acid is produced by the lichens Ramalina , Evernia , and Hypogymnia . [8]

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<span class="mw-page-title-main">Parietinic acid</span> Chemical compound found in some lichens

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<span class="mw-page-title-main">Confluentic acid</span> Chemical compound found in some lichens

Confluentic acid is an organic compound belonging to the chemical class known as depsides. It serves as a secondary metabolite in certain lichens and plays a role in distinguishing closely related species within the genus Porpidia. In 1899, Friedrich Wilhelm Zopf isolated a compound from Lecidea confluens, which he initially named confluentin and noted for its melting point of 147–148 °C. This substance demonstrated the ability to turn litmus paper red and, when interacting with alkali, decomposed into carbon dioxide and phenol-like compounds. Zopf subsequently revised the chemical formula and melting point of the compound. Siegfried Huneck renamed it confluentinic acid in 1962, characterising it as optically inactive, with distinct colour reactions and solubility properties, and determined its molecular formula as C28H36O8.

References

  1. "Evernic Acid (CAS 537-09-7)". www.caymanchem.com.
  2. "Evernic acid". pubchem.ncbi.nlm.nih.gov.
  3. 服部植物研究所報告. The Laboratory. p. 84.
  4. Nigg, H. N.; Seigler, D. (29 June 2013). Phytochemical Resources for Medicine and Agriculture. Springer Science & Business Media. p. 206. ISBN   978-1-4899-2584-8.
  5. "Evernsäure". www.internetchemie.info.
  6. Scientific Opinion. p. 227.
  7. Britain), Royal Society (Great. Proceedings of the Royal Society of London. Taylor & Francis. p. 226.
  8. Lee, Seulah; Suh, Yeon Ji; Yang, Seonguk; Hong, Dong Geun; Ishigami, Akihito; Kim, Hangun; Hur, Jae-Seoun; Chang, Seung-Cheol; Lee, Jaewon (20 February 2021). "Neuroprotective and Anti-Inflammatory Effects of Evernic Acid in an MPTP-Induced Parkinson's Disease Model". International Journal of Molecular Sciences. 22 (4): 2098. doi: 10.3390/ijms22042098 . PMC   7924051 . PMID   33672606.

Further reading