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

Zai-Qin ZhengWen-Jun WeiJunmin ZhangHang-Ying LiKai XuJiayuan XuBencan TangYa LiKun Gao
Published in: The Journal of organic chemistry (2019)
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.
Keyphrases
  • induced apoptosis
  • high resolution
  • cell cycle arrest
  • high intensity
  • magnetic resonance imaging
  • magnetic resonance
  • signaling pathway
  • computed tomography
  • dual energy