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(+)- and (-)-Preuisolactone A: A Pair of Caged Norsesquiterpenoidal Enantiomers with a Tricyclo[4.4.01,6.02,8]decane Carbon Skeleton from the Endophytic Fungus Preussia isomera.

Lu-Lin XuHai-Li ChenPing HaiYuan GaoChuan-Dong XieXiao-Long YangLeonard Kaysser
Published in: Organic letters (2019)
A pair of enantiomeric norsesquiterpenoids, (+)- and (-)-preuisolactone A (1) [(+)-1 and (-)-1)] featuring an unprecedented tricyclo[4.4.01,6.02,8]decane carbon scaffold were isolated from Preussia isomera. Their structures were determined by spectroscopic and computed methods and X-ray crystallography. Compounds (+)-1 and (-)-1 are two rare naturally occurring sesquiterpenoidal enantiomers. A plausible biosynthetic pathway for 1 is proposed. Additionally, (±)-1 exhibited remarkable antibacterial activity against Micrococcus luteus with an MIC value of 10.2 μM.
Keyphrases
  • capillary electrophoresis
  • high resolution
  • molecular docking
  • mass spectrometry
  • dual energy
  • tissue engineering
  • computed tomography
  • diffusion weighted imaging
  • magnetic resonance
  • molecular dynamics simulations