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Chlorfortunones A and B, Two Sesquiterpenoid Dimers, Possessing Dispiro[4,2,5,2]pentadecane-6,10,14-tren Moiety from Chloranthus fortunei .

Xu-Jia WuDai CaoFei-Long ChenRong-Sheng ShenJin GaoLi-Ping BaiWei ZhangZhi-Hong JiangGuo-Yuan Zhu
Published in: ACS omega (2022)
Chlorfortunones A ( 1 ) and B ( 2 ), two novel sesquiterpenoid dimers, were isolated from the roots of Chloranthus fortunei . Their structures were elucidated by spectroscopic analysis and X-ray diffraction analysis. Compounds 1 and 2 represent a new type of sesquiterpenoid dimer possessing an unprecedented 3/5/6/6/6/5 hexacyclic system with a unique dispiro[4,2,5,2]pentadecane-6,10,14-trien moiety. A plausible biosynthetic pathway of 1 and 2 was proposed. Compound 1 showed transforming growth factor (TGF)-β inhibitory activity in MDA-MB-231 cells.
Keyphrases
  • transforming growth factor
  • epithelial mesenchymal transition
  • high resolution
  • induced apoptosis
  • cell cycle arrest
  • computed tomography
  • cell death
  • signaling pathway
  • molecular dynamics simulations
  • dual energy