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Citrinin and α-pyrone derivatives with pancreatic lipase inhibitory activities from Penicillium sp. SCSIO 41302.

Wen-Rong HanMeng-Meng SongYi-Wei HuXiao-Yan PangSheng-Rong LiaoBin YangXue-Feng ZhouYong-Hong LiuQing-Chao LiuJun-Feng Wang
Published in: Journal of Asian natural products research (2021)
One new citrinin monomer derivative (1), and two new natural products α-pyrone analogues (2a and 2b), were isolated from the sponge derived fungus Penicillium sp. SCSIO 41302. Their structures were determined by extensive spectroscopic analysis, chiral-phase HPLC analysis, modified Mosher's method, ECD calculations, and X-ray single-crystal diffraction. Bioactivity screening showed that compounds 2b and 8 exhibited obvious inhibitory activities against pancreatic lipase and acetyl cholinesterase with IC50 values of 48.5 and 4.8 μM, respectively, which indicated that different chiral center between enantiomers (2a and 2b) might result in different biological activities (IC50 value against PL for 2a >100 μg/ml).
Keyphrases
  • molecular docking
  • high resolution
  • ms ms
  • molecular dynamics
  • magnetic resonance imaging
  • magnetic resonance
  • density functional theory
  • molecularly imprinted
  • data analysis
  • electron microscopy