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Chemical Compound Review

Parmelin     methyl4-(2,4-dihydroxy-3- methanoyl-6...

Synonyms: Atranorin, Usnarin, Atranorine, Atranoric acid, Parmelin acid, ...
 
 
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Disease relevance of Atranorine

 

High impact information on Atranorine

  • Identification of atranorin and related potential allergens in oakmoss absolute by high-performance liquid chromatography-tandem mass spectrometry using negative ion atmospheric pressure chemical ionization [3].
  • Our first results showed that atranol and chloroatranol, formed by transesterification and decarboxylation of the lichen depsides, atranorin and chloroatranorin, during the preparation of oak moss absolute, are strong elicitants in most patients sensitized to oak moss [4].
  • Methyl beta-orcinolcarboxylate (2), ethyl hematommate (3), the didepside atranorin (4), and (+)-protolichesterinic acid (7) did not influence keratinocyte growth at concentrations of 5 microM [5].
  • Atranorin was the only lichen acid with no significant effect on ATPase [6].
 

Analytical, diagnostic and therapeutic context of Atranorine

References

  1. Airborne contact dermatitis from atranorin. Lorenzi, S., Guerra, L., Vezzani, C., Vincenzi, C. Contact Derm. (1995) [Pubmed]
  2. Photohemolytic activity of lichen metabolites. Hidalgo, M.E., Fernández, E., Quilhot, W., Lissi, E.A. J. Photochem. Photobiol. B, Biol. (1993) [Pubmed]
  3. Identification of atranorin and related potential allergens in oakmoss absolute by high-performance liquid chromatography-tandem mass spectrometry using negative ion atmospheric pressure chemical ionization. Hiserodt, R.D., Swijter, D.F., Mussinan, C.J. Journal of chromatography. A. (2000) [Pubmed]
  4. Contact allergy to oak moss: search for sensitizing molecules using combined bioassay-guided chemical fractionation, GC-MS, and structure-activity relationship analysis. Bernard, G., Giménez-Arnau, E., Rastogi, S.C., Heydorn, S., Johansen, J.D., Menné, T., Goossens, A., Andersen, K., Lepoittevin, J.P. Arch. Dermatol. Res. (2003) [Pubmed]
  5. Lichen metabolites. 2. Antiproliferative and cytotoxic activity of gyrophoric, usnic, and diffractaic acid on human keratinocyte growth. Kumar, K.C., Müller, K. J. Nat. Prod. (1999) [Pubmed]
  6. Lichen acids as uncouplers of oxidative phosphorylation of mouse-liver mitochondria. Abo-Khatwa, A.N., al-Robai, A.A., al-Jawhari, D.A. Nat. Toxins (1996) [Pubmed]
  7. Contact allergy to atranorin in lichens and perfumes. Dahlquist, I., Fregert, S. Contact Derm. (1980) [Pubmed]
 
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