Anti-Neuroinflammatory Meroterpenoids from a Chinese Collection of the Brown Alga Sargassum siliquastrum .
Yu QiZhongle WangJingwen ZhangShuhua TangHaoyun ZhuBing JiangXinhua LiJiabao WangZhongmin SunMin ZhaoHaoru ZhuPengcheng YanPublished in: Journal of natural products (2023)
Nine new chromane-type meroterpenoids, including the rare nor-meroterpenoid sargasilol A ( 1 ) and the eight meroditerpenoids sargasilols B-I ( 2 - 9 ), were isolated from a China Sea collection of the brown alga Sargassum siliquastrum , together with six known analogues ( 10 - 15 ). The structures of the new chromanes were identified by extensive spectroscopic analysis and by comparison with previously reported data. Compounds 1 - 3 and 6 - 15 exhibited inhibition against LPS-induced NO production in BV-2 microglial cells, and 1 , with a shorter carbon chain, was the most active one. Compound 1 was established as an anti-neuroinflammatory agent through targeting the IKK/IκB/NF-κB signaling pathway. As such, the chromanes from brown algae could provide promising anti-neuroinflammatory lead compounds for further structural modification.
Keyphrases
- lps induced
- inflammatory response
- induced apoptosis
- signaling pathway
- molecular docking
- pi k akt
- cell cycle arrest
- endoplasmic reticulum stress
- lipopolysaccharide induced
- electronic health record
- big data
- toll like receptor
- high resolution
- machine learning
- cancer therapy
- spinal cord injury
- cell death
- immune response
- spinal cord
- molecular dynamics simulations
- drug delivery
- data analysis
- nuclear factor