4.4 Article

One new furanone analogue from the deep-sea fungus Purpureocillium sp. SCSIO 06693

期刊

NATURAL PRODUCT RESEARCH
卷 37, 期 20, 页码 3512-3518

出版社

TAYLOR & FRANCIS LTD
DOI: 10.1080/14786419.2022.2089671

关键词

Deep-sea fungus; Purpureocillium sp; furanone analog; antioxidant; pancreatic lipase

向作者/读者索取更多资源

A new furanone analog and six known compounds were isolated from a deep-sea fungus. One of the compounds exhibited modest antioxidant activity while others showed pancreatic lipase inhibitory activities.
A new furanone analog, (E)-2-(8,9-dihydroxy-6,8-dimethyldec-4-en-2-yl)-met-hylfuran-3(2H)-one (1), together with six known compounds, including two diterpenoids (2 and 3), one butyrolactone (4) and three isocoumarins (5-7), were isolated from a deep-sea fungus, Purpureocillium sp. SCSIO 06693. Among them, compound 1 existed as two tautomeric forms (1a and 1b) differing in configuration of the furan ring. The chemical structures were elucidated by the basis of spectroscopic evidences, including HRESIMS, NMR and optical rotation. Isolated compounds were evaluated for their cytotoxic, antiviral, antibacterial, antioxidant, acetyl cholinesterase (AChE) and pancreatic lipase (PL) enzyme inhibitory activities. Biological evaluation results revealed that compound 4 showed modest antioxidant activity against DPPH with IC50 value of 72.03 mu M. In addition, compounds 1-4 exhibited PL enzyme inhibitory activities.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.4
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据