Communiferulins, farnesylated coumarins from the roots of Ferula communis and their anti-neuroinflammatory activity.
Yuki YoshinoNaonobu TanakaDaisuke TsujiKohji ItohYoshiki KashiwadaPublished in: Journal of natural medicines (2022)
Three new farnesylated coumarins, communiferulins A-C (1-3), and a farnesylated chromone, ferchromone (4), were isolated from the roots of an Apiaceous plant Ferula communis. Their structures including the relative configurations were elucidated by a combination of spectroscopic analyses and calculations of the NMR data. Communiferulins A-C (1-3) had dihydrofuran rings fused to C-3 and C-4 of their coumarin moieties, while 3 possessed one additional furan ring. HPLC analyses using a chiral column showed 1-4 to be racemates, and the absolute configurations of (+)-1, (-)-1, (+)-2, and (-)-2 were deduced by comparison of their ECD spectra with TDDFT-calculated spectra. Communiferulins A (1) and B (2), and ferchromone (4) showed inhibitory activities on IL-1β production from LPS-stimulated microglial cells.
Keyphrases
- density functional theory
- inflammatory response
- induced apoptosis
- high resolution
- ms ms
- cell cycle arrest
- solid phase extraction
- molecular docking
- molecular dynamics
- lipopolysaccharide induced
- simultaneous determination
- magnetic resonance
- molecular dynamics simulations
- lps induced
- electronic health record
- mass spectrometry
- high performance liquid chromatography
- liquid chromatography
- neuropathic pain
- tandem mass spectrometry
- anti inflammatory
- cell death
- fluorescent probe
- signaling pathway
- capillary electrophoresis
- oxidative stress
- spinal cord
- spinal cord injury
- deep learning