Heliaquanoids A-E, Five Sesquiterpenoid Dimers from Inula helianthus-aquatica

J Org Chem. 2019 Apr 5;84(7):4473-4477. doi: 10.1021/acs.joc.8b03284. Epub 2019 Mar 27.

Abstract

Heliaquanoid A (1), the first exo-2,4-linked Diels-Alder adduct between a pseudoguaianolide dienophile and a guaianolide diene, and heliaquanoids B-E (2-5), four new 2,4-linked Diels-Alder adducts between a xanthanolide dienophile and a guaianolide diene, were isolated from stems and leaves of Inula helianthus-aquatica. Their structures were determined by NMR spectroscopy, a modified Mosher's method, electronic circular dichroism, and X-ray diffraction analysis. Compounds 2 and 3 exhibited moderate cytotoxic activities against HL-60 cells with IC50 values of 7.5 and 4.9 μM, respectively.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • A549 Cells
  • Antineoplastic Agents / chemistry
  • Antineoplastic Agents / isolation & purification
  • Antineoplastic Agents / pharmacology
  • Cell Line, Tumor
  • Crystallography, X-Ray
  • Dimerization
  • Drug Screening Assays, Antitumor
  • HL-60 Cells
  • Helianthus / chemistry
  • Humans
  • Inula / chemistry*
  • MCF-7 Cells
  • Models, Molecular
  • Nuclear Magnetic Resonance, Biomolecular
  • Sesquiterpenes / chemistry*
  • Sesquiterpenes / isolation & purification
  • Sesquiterpenes / pharmacology

Substances

  • Antineoplastic Agents
  • Sesquiterpenes