Septosones A-C, in Vivo Anti-inflammatory Meroterpenoids with Rearranged Carbon Skeletons from the Marine Sponge Dysidea septosa.
Yu-Han GuiHou-Wen LinMi ZhouYun ZhangDe-Quan ZengHong-Rui ZhuKe-Chun LiuFan SunHai-Feng ChenHou-Wen LinPublished in: Organic letters (2019)
Three unusual meroterpenoids, septosones A-C (1-3), were isolated from the marine sponge Dysidea septosa. The structures were determined by analysis of spectroscopic data combined with single-crystal X-ray diffraction and ECD calculations. Septosone A (1) features an unprecedented "septosane" carbon skeleton, whereas septosones B (2) and C (3) share a rare spiro[4.5]decane motif. Septosone A showed in vivo anti-inflammatory activity in CuSO4-induced transgenic fluorescent zebrafish likely through inactivation of the NF-κB signaling pathway.
Keyphrases
- signaling pathway
- pi k akt
- anti inflammatory
- high resolution
- diabetic rats
- high glucose
- molecular docking
- induced apoptosis
- epithelial mesenchymal transition
- quantum dots
- density functional theory
- electronic health record
- oxidative stress
- molecular dynamics simulations
- lps induced
- electron microscopy
- big data
- living cells
- magnetic resonance imaging
- drug induced
- endothelial cells
- dual energy
- cell proliferation
- magnetic resonance
- machine learning
- immune response
- artificial intelligence
- inflammatory response
- crystal structure