Desaspidin

Chemical compound
  • P02DX01 (WHO)
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
  • 114-43-2 checkY
PubChem CID
  • 8238
ChemSpider
  • 10295071 ☒N
UNII
  • KV3495SGKS
KEGG
  • D07365 checkY
ChEMBL
  • ChEMBL2105606 ☒N
CompTox Dashboard (EPA)
  • DTXSID00976317 DTXSID6074461, DTXSID00976317 Edit this at Wikidata
ECHA InfoCard100.003.680 Edit this at WikidataChemical and physical dataFormulaC24H30O8Molar mass446.496 g·mol−13D model (JSmol)
  • Interactive image
  • 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
  • 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 ☒N
  • Key:GAHOBHHMYUYJDT-UHFFFAOYSA-N ☒N
 ☒NcheckY (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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Antiparasitics – Anthelmintics (P02) and endectocides (QP54)
Antiplatyhelmintic agents
Antitrematodals
(schistosomicides)
Binds tubulin
AChE inhibitor
Other/unknown
Anticestodals
(taeniacides)
Binds tubulin
Other/unknown
Antinematodal agents
(including
macrofilaricides)
Binds tubulin
Glutamate-gated chloride channel, GABA receptor
NMDA
Other/unknown
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