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Two new serratene triterpenes from club moss cultivars.

Wachirasak ThaisaengWanlaya ThamnarakSomsak RuchirawatKittipong ChainokNopporn Thasana
Published in: Natural product research (2023)
Two new serratene triterpenes, 14α,21β-dihydroxyserrat-3β-yl acetate and 3α,21β-dihydroxyserrat-14-en-23-oic acid, together with eight known compounds were isolated from two club moss cultivars, Phlegmariurus carinatus (Desv.) Ching and Phlegmariurus nummulariifolius (Blume) Ching. 14α,21β-Ddihydroxyserrat-3β-yl acetate ( 1 ) was isolated from P. carinatus , and 3α,21β-dihydroxyserrat-14-en-23-oic acid ( 2 ), an undescribed carboxylic group at C-23 position of the serratene triterpenoids, was isolated from P. nummulariifolius . The structures of these new compounds were elucidated by using HR-ESIMS, UV, IR, 1D ( 1 H and 13 C NMR spectra), 2D NMR spectra, experimental ECD spectrometry and the single-crystal X-ray analysis. Biological evaluation of 14α,21β-dihydroxyserrat-3β-yl acetate ( 1 ) and lycoclavanol ( 8 ) revealed moderate cytotoxic activity on three tumor cell lines (HepG2, A549 and HuCCA-1) whereas 3α,21β-dihydroxyserrat-14-en-23-oic acid ( 2 ) showed strong inhibitory effect on HuCCA-1 cells with the IC 50 of 4.72 µM.
Keyphrases
  • high resolution
  • magnetic resonance
  • induced apoptosis
  • solid state
  • density functional theory
  • magnetic resonance imaging
  • cell proliferation
  • signaling pathway
  • endoplasmic reticulum stress