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17- nor-Cephalotane-Type Diterpenoids from Cephalotaxus fortunei.

Zhan-Peng GeHong-Chun LiuGuo-Cai WangQun-Fang LiuCheng-Hui XuJian DingYao-Yue FanJian-Min Yue
Published in: Journal of natural products (2019)
Seventeen new 17- nor-cephalotane-type diterpenoids, fortalpinoids A-Q (1-17), were isolated from the seeds of Cephalotaxus fortunei var. alpine. Compound 12 represents the first 17- nor-cephalotane-type diterpenoid featuring an 8-oxabicyclo[3.2.1]oct-2-ene moiety. The absolute configuration of fortunolide A (18) was determined for the first time, and the structure of cephinoid Q was revised to 14- epi-cephafortoid A (24) by X-ray crystallographic data analysis. Some of the compounds showed significant cytotoxicity against A549 and HL-60 cells, and the structure-activity relationship of this compound class is discussed.
Keyphrases
  • data analysis
  • structure activity relationship
  • induced apoptosis
  • cell proliferation
  • cell cycle arrest
  • signaling pathway
  • mass spectrometry
  • endoplasmic reticulum stress