SANC00430



Eucannabinolide





C22H28O8













38458-58-1



SMILES:

[H][C@@]12C=C(C)[C@@H](OC(C)=O)CC=C(C)C[C@@H](OC(=O)/C(=C/CO)CO)[C@@]1([H])C(=C)C(=O)O2





References

  • Fouche et al. (2008) In vitro anticancer screening of South African plants

  • Classifications

  • Sesquiterpene

  • Terpenoid

  • Other Names

  • 2-Butenoic Acid, 4-Hydroxy-2-(Hydroxymethyl)-, (3Ar,4R,6E,9S,10Z,11Ar)-9-(Acetyloxy)-2,3,3A,4,5,8,9,11A-Octahydro-6,10-Dimethyl-3-Methylene-2-Oxocyclodeca[B]Furan-4-Yl Ester, (2E)
  • 2-Butenoic Acid, 4-Hydroxy-2-(Hydroxymethyl)-, 9-(Acetyloxy)-2,3,3A,4,5,8,9,11A-Octahydro-6,10-Dimethyl-3-Methylene-2-Oxocyclodeca[B]Furan-4-Yl Ester, [3Ar-[3Ar*,4R*(E),6E,9S*,10Z,11Ar*]]
  • Eucannabinolid
  • Hiyodorilactone A
  • Schkuhrin I

  • Source Organisms

  • Schkuhria pinnata

    Compound Uses

  • Anticancer activity