Aculeatiols A-G: Lovastatin Derivatives Extracted from Aspergillus aculeatus .
Fei LiuXinyi QiaoQin LiJiajun ZhouJie GaoFeng HePeng WuChunmei ChenWeiguang SunHucheng ZhuYong-Hui ZhangPublished in: Journal of natural products (2024)
In this study, we isolated lovastatin derivatives, including aculeatiols A-G ( 1 - 7 ) and three known compounds ( 8 - 10 ), from Aspergillus aculeatus . Their structures and absolute configurations were experimentally determined by high-resolution electrospray ionization mass spectrometry, nuclear magnetic resonance spectroscopy, and X-ray diffraction analyses, and the results were corroborated by quantum-chemical calculations. As members of the lovastatin derivatives, aculeatiols A-C ( 1 - 3 ) possess a γ-lactone functional group in the side chain. Compound 6 represents the first example that features an undescribed aromatized heterotetracyclic 6/6/6/6 ring system. Biologically, the lipid-lowering effects of all of these compounds were evaluated by analyzing the free fatty acid-induced intracellular lipid accumulation. In addition, compound 5 , which regulated the transcription of genes associated with lipid uptake and synthesis, inhibited the accumulation of lipids.
Keyphrases
- high resolution
- mass spectrometry
- fatty acid
- molecular dynamics
- transcription factor
- structure activity relationship
- liquid chromatography
- computed tomography
- molecular dynamics simulations
- gas chromatography
- high performance liquid chromatography
- reactive oxygen species
- monte carlo
- capillary electrophoresis
- ms ms