Login / Signup

Strophioblachins A-K, Structurally Intriguing Diterpenoids from Strophioblachia fimbricalyx with Potential Anticardiac Hypertrophic Inhibitory Activity.

Xiong QiuYong-Xiang HuangJing YuanXue-Dan ZuYa-Ling ZhouRui LiZe-Kai WuWei-Lie XiaoChang-Bo ZhengXiao-Li Li
Published in: Journal of natural products (2023)
Three new rearranged diterpenoids, strophioblachins A-C ( 1 - 3 ), eight new diterpenoids, strophioblachins D-K ( 4 - 11 ), and seven previously described diterpenoids ( 12 - 18 ) were purified from the aerial parts of Strophioblachia fimbricalyx. Compounds 1 and 2 contain a rare 6/6/5/6 ring system, while 3 has an uncommon tricyclo[4.4.0.0 8,9 ]tridecane-bridged unit, and their diterpenoid skeletons are being reported for the first time. Utilizing spectroscopic and HRESIMS data analysis, the structures of the new compounds ( 1 - 11 ) were established, and ECD and 13 C NMR calculations were used to confirm the relative and absolute configurations of 11 and 9 . The absolute configurations of compounds 1 , 3 , and 10 were established using single-crystal X-ray diffraction. The results of testing for anticardiac hypertrophic activity demonstrated that compounds 10 and 15 dose-dependently lowered the mRNA expression of Nppa and Nppb . Protein levels were confirmed by Western blotting, which also demonstrated that compounds 10 and 15 lowered the expression of the hypertrophic marker ANP. The cytotoxic activity against neonatal rat cardiomyocytes was assayed in vitro by the CCK-8 and ELISA methods, and the results showed that compounds 10 and 15 were only very weakly active in the range.
Keyphrases
  • data analysis
  • high resolution
  • poor prognosis
  • oxidative stress
  • magnetic resonance imaging
  • south africa
  • molecular docking
  • long non coding rna
  • binding protein
  • solid state
  • amino acid
  • endothelial cells