Usnic acid
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Names | |
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IUPAC name
2,6-Diacetyl-7,9-dihydroxy-8,9b-dimethyldibenzo[b,d]furan-1,3(2H,9bH)-dione
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Other names
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Identifiers | |
3D model (JSmol)
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ChEBI | |
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.004.310 |
PubChemCID
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UNII |
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CompTox Dashboard(EPA)
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Properties | |
C18H16O7 | |
Molar mass | 344.319g·mol−1 |
Melting point | 204 °C (399 °F; 477 K) |
<0.001 g/L (25°C)[1] | |
Solubilityinacetone | 0.077 g/L[1] |
Solubilityinethyl acetate | 0.088 g/L[1] |
Solubilityinfurfural | 0.732 g/L[1] |
Solubilityinfurfuryl alcohol | 0.121 g/L[1] |
Except where otherwise noted, data are given for materials in theirstandard state(at 25 °C [77 °F], 100 kPa).
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Usnic acidis a naturally occurringdibenzofuranderivative found in severallichenspecies with the formula C18H16O7.It was first isolated by German scientist W. Knop in 1844[2]and first synthesized between 1933 and 1937 by Curd and Robertson.[3]Usnic acid was identified in many genera of lichens includingUsnea,Cladonia,Hypotrachyna,Lecanora,Ramalina,Evernia,ParmeliaandAlectoria.Although it is generally believed that usnic acid is exclusively restricted to lichens, in a few unconfirmed isolated cases the compound was found inkombuchatea and non-lichenizedascomycetes.[4][5]
At normal conditions, usnic acid is a bitter, yellow, solid substance.[6]It is known to occur in nature in both the d- and l-forms as well as aracemicmixture. Salts of usnic acid are called usnates (e.g.copper usnate).
Biological role in lichens
[edit]Usnic acid is a secondary metabolite in lichens whose role has not been completely elucidated. It is believed that usnic acid protects the lichen from adverse effects of sunlight exposure and deters grazing animals with its bitter taste.
Biosynthesis
[edit]Usnic acid is apolyketidebiosynthesized via methylphloroacetophenone as an intermediate.[7]
![](https://upload.wikimedia.org/wikipedia/commons/thumb/d/db/Proposed_biosynthesis_for_usnic_acid.png/400px-Proposed_biosynthesis_for_usnic_acid.png)
Safety
[edit]Usnic acid and its salts are idiosyncratically associated with severehepatotoxicityandliver failure.[8][9]Daily oral intake of 300–1350 mg over a period of weeks has led to severe hepatotoxicity in a number of persons.[10][11]
Sodium usnate was one ingredient in a product called "Lipokinetix" that was claimed to induce weight loss via an increase in metabolic rate. Lipokinetix has been the topic of an FDA warning in the USA[12]due to potential hepatotoxicity, although it is unclear yet if any toxicity would be attributable to the aforementioned salt. Lipokinetix also containednorephedrine(PPA),caffeine,yohimbineand3,5-diiodothyronine.
Pharmacology
[edit]Usnic acid has been found to haveadrenergic activityin both frog and earthworm nerve junction models in preliminary research.[13]
Analytics
[edit]It is possible to determine the content of usnic acid inlichenextractusing reversed-polaritycapillary zone electrophoresisorhigh performance liquid chromatographyanalysis.[14]
References
[edit]- ^abcdeO'Neil, Maryadele J.; Merck Sharp and Dohme Research Laboratories, eds. (2001).The Merck index: an encyclopedia of chemicals, drugs, and biologicals(13th ed.). Whitehouse Station, NJ: Merck. p. 1762.ISBN978-0-911910-13-1.
{{cite book}}
:CS1 maint: date and year (link) - ^Knop, W (1844)."Chemisch-physiologische Untersuchung uber die Flechten".Annalen der Chemie und Pharmacie.49(2): 103–124.doi:10.1002/jlac.18440490202.
- ^Robertson, A.; Curd, F. H. (1933). "277. Usnic acid. Part III. Usnetol, usnetic acid, and pyrousnic acid".Journal of the Chemical Society (Resumed):1173.doi:10.1039/jr9330001173.
- ^Cocchietto, Moreno; Skert, Nicola; Nimis, Pier; Sava, Gianni (2002). "A review on usnic acid, an interesting natural compound".Naturwissenschaften.89(4): 137–146.Bibcode:2002NW.....89..137C.doi:10.1007/s00114-002-0305-3.ISSN0028-1042.PMID12061397.S2CID11481018.
- ^Blanc, Philippe J. (1996). "Characterization of the tea fungus metabolites".Biotechnology Letters.18(2): 139–142.doi:10.1007/BF00128667.ISSN0141-5492.S2CID34822312.
- ^Michael Ash; Irene Ash (2004).Handbook of preservatives.Synapse Info Resources. p. 5856.ISBN978-1-890595-66-1.Retrieved5 August2010.
- ^Taguchi, Heihachiro; Sankawa, Ushio; Shibata, Shoji (1969)."Biosynthesis of Natural Products. VI. Biosynthesis of Usnic Acid in Lichens. (1). A General Scheme of Biosynthesis of Usnic Acid".Chemical & Pharmaceutical Bulletin.17(10): 2054–2060.doi:10.1248/cpb.17.2054.PMID5353559.
- ^Chitturi, Shivakumar; Farrell, Geoffrey C. (2008). "Hepatotoxic slimming aids and other herbal hepatotoxins".Journal of Gastroenterology and Hepatology.23(3): 366–373.doi:10.1111/j.1440-1746.2008.05310.x.PMID18318821.S2CID23840983.
- ^Yellapu RK, Mittal V, Grewal P, Fiel M, Schiano T (2011)."Acute liver failure caused by 'fat burners' and dietary supplements: a case report and literature review".Canadian Journal of Gastroenterology.25(3): 157–60.doi:10.1155/2011/174978.PMC3076034.PMID21499580.
- ^Hsu, LM; Huang, YS; Chang, FY; Lee, SD (Jul 2005). "'Fat burner' herb, usnic acid, induced acute hepatitis in a family ".Journal of Gastroenterology and Hepatology.20(7): 1138–9.doi:10.1111/j.1440-1746.2005.03855.x.PMID15955234.S2CID6717430.
- ^Sanchez, William; Maple, John T.; Burgart, Lawrence J.; Kamath, Patrick S. (2006). "Severe Hepatotoxicity Associated with Use of a Dietary Supplement Containing Usnic Acid".Mayo Clinic Proceedings.81(4): 541–544.doi:10.4065/81.4.541.PMID16610575.
- ^"Safety Alerts for Human Medical Products > Lipokinetix".MedWatch: The FDA Safety Information and Adverse Event Reporting Program.U.S. Food and Drug Administration. November 20, 2001.Retrieved5 December2012.
FDA has received multiple reports of persons who developed liver injury or liver failure while using Lipokinetix. The product contains norephedrine (also known as phenylpropanolamine or PPA), caffeine, yohimbine, diiodothyronine, and sodium usniate.
- ^Harris N. J. (1961), Honors Thesis, Clark University, Worcester, Massachusetts
- ^Kreft, Samo; Štrukelj, Borut (2001). "Reversed-polarity capillary zone electrophoretic analysis of usnic acid".Electrophoresis.22(13): 2755–2757.doi:10.1002/1522-2683(200108)22:13<2755::AID-ELPS2755>3.0.CO;2-6.PMID11545403.S2CID24341350.
External links
[edit]- Seeking to Fight Fat, She Lost Her Liver,New York Times,March 4, 2003