New Thiodiketopiperazine and 3,4-Dihydroisocoumarin Derivatives from the Marine-Derived Fungus Aspergillus terreus.
Jing-Shuai WuXiao-Hui ShiGuang-Shan YaoChang-Lun ShaoXiu-Mei FuXiu-Li ZhangHua-Shi GuanChang-Yun WangPublished in: Marine drugs (2020)
Aspergillus terreus has been reported to produce many secondary metabolites that exhibit potential bioactivities, such as antibiotic, hypoglycemic, and lipid-lowering activities. In the present study, two new thiodiketopiperazines, emestrins L (1) and M (2), together with five known analogues (3-7), and five known dihydroisocoumarins (8-12), were obtained from the marine-derived fungus Aspergillus terreus RA2905. The structures of the new compounds were elucidated by analysis of the comprehensive spectroscopic data, including high-resolution electrospray ionization mass spectrometry (HRESIMS), one-dimensional (1D) and two-dimensional (2D) nuclear magnetic resonance (NMR), and electronic circular dichroism (ECD) data. This is the first time that the spectroscopic data of compounds 3, 8, and 9 have been reported. Compound 3 displayed antibacterial activity against Pseudomonas aeruginosa (minimum inhibitory concentration (MIC) = 32 μg/mL) and antifungal activity against Candida albicans (MIC = 32 μg/mL). In addition, compound 3 exhibited an inhibitory effect on protein tyrosine phosphatase 1 B (PTP1B), an important hypoglycemic target, with an inhibitory concentration (IC)50 value of 12.25 μM.
Keyphrases
- high resolution
- magnetic resonance
- candida albicans
- mass spectrometry
- molecular docking
- pseudomonas aeruginosa
- electronic health record
- biofilm formation
- big data
- rheumatoid arthritis
- cell wall
- escherichia coli
- systemic sclerosis
- tandem mass spectrometry
- fatty acid
- binding protein
- ankylosing spondylitis
- contrast enhanced
- protein kinase
- multidrug resistant
- gas chromatography
- interstitial lung disease
- simultaneous determination