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Fumarprotocetraric acid

From Wikipedia, the free encyclopedia
Fumarprotocetraric acid
Names
IUPAC name
4-[[(E)-3-Carboxyprop-2-enoyl]oxymethyl]-10-formyl-3,9-dihydroxy-1,7-dimethyl-6-oxobenzo[b][1,4]benzodioxepine-2-carboxylic acid
Other names
Fumaroprotocetraric acid
Identifiers
3D model (JSmol)
ECHA InfoCard 100.006.999 Edit this at Wikidata
  • InChI=1S/C22H16O12/c1-8-5-12(24)10(6-23)19-15(8)22(31)34-20-11(7-32-14(27)4-3-13(25)26)17(28)16(21(29)30)9(2)18(20)33-19/h3-6,24,28H,7H2,1-2H3,(H,25,26)(H,29,30)/b4-3+
    Key: VEGGRTFDFMUBPD-ONEGZZNKSA-N
  • CC1=CC(=C(C2=C1C(=O)OC3=C(O2)C(=C(C(=C3COC(=O)/C=C/C(=O)O)O)C(=O)O)C)C=O)O
Properties
C22H16O12
Molar mass 472.358 g·mol−1
Appearance Colorless, odorless solid with bitter taste[1]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Fumarprotocetraric acid is a chemical compound with the chemical formula C22H16O12. It is a secondary metabolite produced by a variety of lichens.

Occurence

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Fumarprotocetraric acid is mainly known for its occurrence in Iceland moss (Cetraria islandica), where it is present in a mass fraction of 1–2% (dried thallus).[2]

In addition, fumarprotocetraric acid has been detected in many other lichens, including:

Pharmacology research

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Fumarprotocetraric acid has antibacterial activity.[1] It also induces an immunostimulating effect in vitro by triggering the formation of hydrogen peroxide.[1] Furthermore, cytotoxicity against two cancer cell lines has been demonstrated.[1]

References

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  1. ^ a b c d e Entry on Fumarprotocetrarsäure. at: Römpp Online. Georg Thieme Verlag, retrieved January 5, 2025.
  2. ^ Egon Stahl, Werner Schild (1986). Isolierung und Charakterisierung von Naturstoffen (1st ed.). Stuttgart/New York: Gustav Fischer Verlag. p. 92.
  3. ^ a b c d e f g h i j k l m Wilhelm Zopf (1907). Die Flechtenstoffe in chemischer, botanischer, pharmakologischer und technischer Beziehung (1st ed.). Gustav Fischer Verlag. pp. 172–176.
  4. ^ a b c d e f g h i j k l m n o p q r s t u v w Emil Abderhalden, ed. (1912), Biochemisches Handlexikon. Gerbstoffe, Flechtenstoffe, Saponine, Bitterstoffe, Terpene, Ätherische Öle, Harze, Kautschuk (1. Auflage ed.), Berlin/Heidelberg: Springer Verlag, pp. 74 f