Hepialiamides A-C: Aminated Fusaric Acid Derivatives and Related Metabolites with Anti-Inflammatory Activity from the Deep-Sea-Derived Fungus Samsoniella hepiali W7.
Zheng-Biao ZouTai-Zong WuLong-He YangXi-Wen HeWen-Ya LiuKai ZhangXian-Wen YangMing-Min XieYong ZhangXian-Wen YangJun-Song WangPublished in: Marine drugs (2023)
A systematic investigation combined with a Global Natural Products Social (GNPS) molecular networking approach, was conducted on the metabolites of the deep-sea-derived fungus Samsoniella hepiali W7, leading to the isolation of three new fusaric acid derivatives, hepialiamides A-C ( 1 - 3 ) and one novel hybrid polyketide hepialide ( 4 ), together with 18 known miscellaneous compounds ( 5 - 22 ). The structures of the new compounds were elucidated through detailed spectroscopic analysis. as well as TD-DFT-based ECD calculation. All isolates were tested for anti-inflammatory activity in vitro. Under a concentration of 1 µM, compounds 8 , 11 , 13 , 21 , and 22 showed potent inhibitory activity against nitric oxide production in lipopolysaccharide (LPS)-activated BV-2 microglia cells, with inhibition rates of 34.2%, 30.7%, 32.9%, 38.6%, and 58.2%, respectively. Of particularly note is compound 22, which exhibited the most remarkable inhibitory activity, with an IC 50 value of 426.2 nM.