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Microascones, Decahydrofluorene-Class Alkaloids from the Marine-Derived Fungus Microascus sp. SCSIO 41821.

Fei-Hua YaoXiao LiangWen-Bin ShenXin-Hua LuGuo-Chao LiShu-Hua Qi
Published in: Journal of natural products (2024)
Eight new decahydrofluorene-class alkaloids, microascones A and B ( 1 and 2 ), 2,3-epoxyphomapyrrolidone C ( 3 ), 14,16-epiascomylactam B ( 4 ), 24-hydroxyphomapyrrolidone A ( 5 ), and microascones C-E ( 6 - 8 ), along with five known analogs ( 9 - 13 ) were isolated from the marine-derived fungus Microascus sp. SCSIO 41821. Compounds 1 and 2 have an unprecedented complex macrocyclic alkaloid skeleton with a 6/5/6/5/6/5/13 polycyclic system. Their structures and absolute configurations were determined by spectroscopic analysis, quantum chemical calculations of ECD spectra, and 13 C NMR chemical shifts. Compounds 10 - 13 showed selective enzyme inhibitory activity against PTPSig, PTP1B, and CDC25B, and 4 , 9 , and 10 exhibited strong antibacterial activity against seven tested pathogens. Their structure-bioactivity relationship was discussed, and a plausible biosynthetic pathway for 1 - 8 was also proposed.
Keyphrases
  • molecular docking
  • molecular dynamics
  • density functional theory
  • high resolution
  • magnetic resonance
  • molecular dynamics simulations
  • monte carlo
  • gram negative
  • antimicrobial resistance
  • cell proliferation
  • solid state