Chemical investigation of marine fungus Nigrospora oryzae SYSU-MS0024 cultured on solid-rice medium led to the isolation of three new alkaloids, including a pair of epimers, nigrosporines A ( 1 ) and B ( 2 ), and a pair of enantiomers, (+)-nigrosporine C (+)- 3 , and (-)-nigrosporine C (-)- 3 , together with eight known compounds ( 4 - 11 ). Their structures were elucidated based on extensive mass spectrometry (MS) and 1D/2D nuclear magnetic resonance (NMR) spectroscopic analyses and compared with data in the literature. The absolute configurations of compounds 1 - 3 were determined by a combination of electronic circular dichroism (ECD) calculations, Mosher's method, and X-ray single-crystal diffraction technique using Cu Kα radiation. In bioassays, compound 2 exhibited moderate inhibition on NO accumulation induced by lipopolysaccharide (LPS) on BV-2 cells in a dose-dependent manner at 20, 50, and 100 μmol/L and without cytotoxicity in a concentration of 100.0 μmol/L. Moreover, compound 2 also showed moderate acetylcholinesterase (AChE) inhibitory activities with IC 50 values of 103.7 μmol/L. Compound 5 exhibited moderate antioxidant activity with EC 50 values of 167.0 μmol/L.
Keyphrases
- mass spectrometry
- high resolution
- magnetic resonance
- capillary electrophoresis
- high intensity
- liquid chromatography
- multiple sclerosis
- ms ms
- inflammatory response
- gas chromatography
- high performance liquid chromatography
- induced apoptosis
- lps induced
- systematic review
- cell cycle arrest
- molecular docking
- endothelial cells
- lipopolysaccharide induced
- molecular dynamics
- tandem mass spectrometry
- density functional theory
- toll like receptor
- big data
- solid state
- magnetic resonance imaging
- electronic health record
- contrast enhanced
- radiation therapy
- cell death
- anti inflammatory
- electron microscopy
- signaling pathway
- dual energy