Desaspidin

Last updated
Desaspidin
Desaspidin.svg
Clinical data
ATC code
Identifiers
  • 2-Butanoyl-4-[(3-butanoyl-2,4-dihydroxy-6-methoxyphenyl)methyl]-3,5-dihydroxy-6,6-dimethylcyclohexa-2,4-dien-1-one
CAS Number
PubChem CID
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard (EPA)
ECHA InfoCard 100.003.680 OOjs UI icon edit-ltr-progressive.svg
Chemical and physical data
Formula C24H30O8
Molar mass 446.496 g·mol−1
3D model (JSmol)
  • CCCC(=O)C1=C(C(=C(C=C1O)OC)CC2=C(C(C(=C(C2=O)C(=O)CCC)O)(C)C)O)O
  • InChI=1S/C24H30O8/c1-6-8-14(25)18-16(27)11-17(32-5)12(20(18)28)10-13-21(29)19(15(26)9-7-2)23(31)24(3,4)22(13)30/h11,27-28,30-31H,6-10H2,1-5H3 X mark.svgN
  • Key:GAHOBHHMYUYJDT-UHFFFAOYSA-N X mark.svgN
 X mark.svgNYes check.svgY  (what is this?)    (verify)

Desaspidin is an anthelmintic. Desapidin may occur in natural form within some plants such as Coastal woodfern, Dryopteris arguta . [1] Since the 1950s the inhibition effects of desapidins upon phosphorylation in chloroplasts has been noted and studied. [2]

References

  1. ↑ Hogan CM (2008). Stromberg M (ed.). "Coastal Woodfern (Dryopteris arguta)". GlobalTwitcher. Archived from the original on 2011-07-11.
  2. ↑ Bacon K (2001). Photosynthesis : photobiochemistry and photobiophysics. Dordrecht: Kluwer Academic Publishers. ISBN   0-7923-6791-X.
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